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        <title>Cancer Chemotherapy and Pharmacology via MedWorm.com</title>
        <description>MedWorm.com provides a medical RSS filtering service. Over 6000 RSS medical sources are combined and output via different filters. This feed contains the latest items from the 'Cancer Chemotherapy and Pharmacology' source.</description>
        <link><![CDATA[http://www.medworm.com/rss/search.php?qu=Cancer+Chemotherapy+and+Pharmacology&t=Cancer+Chemotherapy+and+Pharmacology&s=Search&f=source]]></link>
        <lastBuildDate>Wed, 08 Feb 2012 08:41:20 +0100</lastBuildDate>
        <item>
            <title>Gemcitabine in combination with vinorelbine in elderly patients with anthracycline- and taxane-pretreated metastatic breast cancer</title>
            <link>http://www.medworm.com/index.php?rid=5666755&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F0278091141022671%2F</link>
            <description>Conclusion&amp;nbsp;&amp;nbsp;Gemcitabine in combination with vinorelbine is active and safe in elderly patients with anthracycline- and taxane-pretreated
 metastatic breast cancer.
 
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-8DOI 10.1007/s00280-012-1830-1Authors
		Ningning Dong, Key laboratory of Carcinogenesis and Translational Research (Ministry of Education), Medical Oncology Department, Peking University School of Oncology, Beijing Cancer Hospital &amp; Institute, 52 Fucheng Rd, Beijing, 100142 ChinaMingyu Wang, Chemotherapy Department, Shandong Tumor Hospital and Institute, 440 Jiyan Rd, Jinan, 250117 ChinaHuiqing Li, Epidemiology Department, Institute of Basic Medicine, Shandong Academy of Medical Sciences, 18877 Jingshi Rd, Jinan, 250062 ChinaYongchun Cui, Clinical Tr...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5666755</comments>
            <pubDate>Fri, 03 Feb 2012 17:12:25 +0100</pubDate>
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        <item>
            <title>Optimization of patient selection for EGFR-TKIs in advanced non-small cell lung cancer by combined analysis of KRAS, PIK3CA, MET, and non-sensitizing EGFR mutations</title>
            <link>http://www.medworm.com/index.php?rid=5666758&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fdp68w397w2237020%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;When KRAS, PIK3CA, MET, and non-sensitizing EGFR mutations are concomitant, up to 96.0% of NSCLC patients unlikely to respond to TKIs can be identified, and they represented
 independent negative prognostic factors. Comprehensive molecular dissection of EGFR signaling pathways should be considered
 to select advanced NSCLC patients for TKIs therapies.
 
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-11DOI 10.1007/s00280-012-1829-7Authors
		V. Ludovini, Medical Oncology Division, S. Maria della Misericordia Hospital, 1, Via G. Dottori, 06132 Perugia, ItalyF. Bianconi, Department of Electronic and Information Engineering, University of Perugia, Perugia, ItalyL. Pistola, Medical Oncology Division, S. Maria della Misericordia Hospital, 1, Via G. Dott...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5666758</comments>
            <pubDate>Thu, 02 Feb 2012 18:11:01 +0100</pubDate>
            <guid isPermaLink="false">5666758</guid>        </item>
        <item>
            <title>Predicting platinum resistance in primary advanced ovarian cancer patients with an in vitro resistance index</title>
            <link>http://www.medworm.com/index.php?rid=5666757&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fm46r69j2h82848vn%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;This in vitro assay predicted primary platinum resistance, without misclassification of sensitive OC patients, and the results
 were significantly associated with PFS. We suggest that samples from primary tumor and metastatic samples have different responses
 to chemotherapy and that exposure to chemotherapy might induce in vitro platinum resistance.
 
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-8DOI 10.1007/s00280-012-1835-9Authors
		Thea Eline Hetland, Departement of Gynecologic Oncology, Norwegian Radium Hospital, Oslo University Hospital, 0424 Oslo, NorwayJanne Kærn, Departement of Gynecologic Oncology, Norwegian Radium Hospital, Oslo University Hospital, 0424 Oslo, NorwayMartina Skrede, Departement of Pathology, Norwegian Radium Hospital...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5666757</comments>
            <pubDate>Thu, 02 Feb 2012 18:11:01 +0100</pubDate>
            <guid isPermaLink="false">5666757</guid>        </item>
        <item>
            <title>Pharmacokinetics and tissue and tumor exposure of CP-31398, a p53-stabilizing agent, in rats</title>
            <link>http://www.medworm.com/index.php?rid=5666756&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fw311gq829n6666r0%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;CP-31398 is bioavailable and has a relatively long elimination half-life, which supports the achievement of plasma steady-state
 levels with a once daily dosing regimen. CP-31398 exhibits a dramatically high volume of distribution, which is consistent
 with its tissue concentrations being much higher than corresponding plasma levels. It is accumulated in colon tumor tissues,
 albeit at lower concentrations than found in liver, skin, and colon.
 
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-6DOI 10.1007/s00280-011-1811-9Authors
		Izet M. Kapetanovic, Chemopreventive Agent Development Research Group, Division of Cancer Prevention, National Cancer Institute, 6130 Executive Blvd., Rm. 2116, Bethesda, MD 20892, USAMiguel Muzzio, Life Sciences Group,...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5666756</comments>
            <pubDate>Thu, 02 Feb 2012 18:11:01 +0100</pubDate>
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        <item>
            <title>RRM1 and ERCC1 expression in peripheral blood versus tumor tissue in gemcitabine/carboplatin-treated advanced non-small cell lung cancer</title>
            <link>http://www.medworm.com/index.php?rid=5666759&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fv2665220xw75522v%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;Advanced NSCLC patients with low RRM1 mRNA expression both in peripheral blood and in tumor tissue could benefit from gemcitabine/carboplatin
 chemotherapy. ERCC1 mRNA expression in tumor tissue may be a predictive and prognostic indicator in advanced NSCLC patients
 receiving gemcitabine/carboplatin chemotherapy.
 
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-11DOI 10.1007/s00280-012-1834-xAuthors
		Guo Bing Zhang, Department of Pharmacy, The First Affiliated Hospital, School of Medicine, Zhejiang University, 79 Qing Chun Street, Hangzhou, 310003 People’s Republic of ChinaJian Chen, Department of Pharmacy, The First Affiliated Hospital, School of Medicine, Zhejiang University, 79 Qing Chun Street, Hangzhou, 310003 People’s Republic of Chin...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5666759</comments>
            <pubDate>Thu, 02 Feb 2012 18:11:00 +0100</pubDate>
            <guid isPermaLink="false">5666759</guid>        </item>
        <item>
            <title>Non-platinum regimens of gemcitabine plus docetaxel versus platinum-based regimens in first-line treatment of advanced non-small cell lung cancer: a meta-analysis on 9 randomized controlled trials</title>
            <link>http://www.medworm.com/index.php?rid=5659397&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fb6l3m543716542t6%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;GD acquired similar survival with platinum-based regimens in first-line treatment of advanced NSCLC. Platinum-based regimens
 had an advantage in TTP and ORR with more grade 3–4 nausea/vomiting, anemia, neutropenia and febrile neutropenia compared
 with GD.
 
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-11DOI 10.1007/s00280-012-1833-yAuthors
		Yong Yu, Department of Respiratory Medicine, The Second Affiliated Hospital of Soochow University, No. 1055 SanXiang Road, Suzhou, 215004 ChinaXun Xu, Department of Respiratory Medicine, The Second Affiliated Hospital of Soochow University, No. 1055 SanXiang Road, Suzhou, 215004 ChinaZiyan Du, Department of Respiratory Medicine, The Second Affiliated Hospital of Soochow University, No. 1055 SanXiang Roa...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5659397</comments>
            <pubDate>Wed, 01 Feb 2012 17:10:03 +0100</pubDate>
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        <item>
            <title>Midostaurin does not prolong cardiac repolarization defined in a thorough electrocardiogram trial in healthy volunteers</title>
            <link>http://www.medworm.com/index.php?rid=5659398&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fj07842u76v4t3133%2F</link>
            <description>Conclusion&amp;nbsp;&amp;nbsp;Midostaurin demonstrated a good safety profile in healthy volunteers, with no prolonged cardiac repolarization or other changes
 on the electrocardiogram.
 
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-9DOI 10.1007/s00280-012-1825-yAuthors
		Adam del Corral, Novartis Oncology, East Hanover, NJ, USACatherine Dutreix, Novartis Oncology, Basel, SwitzerlandAlice Huntsman-Labed, Novartis Oncology, Basel, SwitzerlandSebastien Lorenzo, Novartis Oncology, Basel, SwitzerlandJoel Morganroth, ERT, East Bridgewater, NJ, USARobert Harrell, Osborne Research Center, LLC, Little Rock, AR, USAYanfeng Wang, Novartis Oncology, East Hanover, NJ, USA
	

	
		Journal Cancer Chemotherapy and PharmacologyOnline ISSN 1432-0843Print ISSN 0344-5704 (Source: Cancer Chemothe...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5659398</comments>
            <pubDate>Tue, 31 Jan 2012 16:48:29 +0100</pubDate>
            <guid isPermaLink="false">5659398</guid>        </item>
        <item>
            <title>The effect of multiple doses of rifampin and ketoconazole on the single-dose pharmacokinetics of ridaforolimus</title>
            <link>http://www.medworm.com/index.php?rid=5659399&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F4h63096281567052%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;Rifampin and ketoconazole both have a clinically meaningful effect on the pharmacokinetics of ridaforolimus.
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-7DOI 10.1007/s00280-011-1819-1Authors
		Mark Stroh, Merck Sharp &amp; Dohme Corp., Whitehouse Station, NJ, USAJohn Palcza, Merck Sharp &amp; Dohme Corp., Whitehouse Station, NJ, USAJacqueline McCrea, Merck Sharp &amp; Dohme Corp., Whitehouse Station, NJ, USASabrina Marsilio, Merck Sharp &amp; Dohme Corp., Whitehouse Station, NJ, USASheila Breidinger, Merck Sharp &amp; Dohme Corp., Whitehouse Station, NJ, USADeborah Panebianco, Merck Sharp &amp; Dohme Corp., Whitehouse Station, NJ, USAAmy Johnson-Levonas, Merck Sharp &amp; Dohme Corp., Whitehouse Station, NJ, USAWalter K. Kraft, Department of Pharmacology and Experimental...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5659399</comments>
            <pubDate>Tue, 31 Jan 2012 07:06:12 +0100</pubDate>
            <guid isPermaLink="false">5659399</guid>        </item>
        <item>
            <title>Prognostic significance of MRP5 immunohistochemical expression in glioblastoma</title>
            <link>http://www.medworm.com/index.php?rid=5638075&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F446180hrp5l600w3%2F</link>
            <description>Conclusion&amp;nbsp;&amp;nbsp;The present results imply that MRP5 index may hold a prognostic role in patients with GBM.
 
 
 
	Content Type Journal ArticleCategory Short CommunicationPages 1-5DOI 10.1007/s00280-012-1832-zAuthors
		George A. Alexiou, Department of Neurosurgery, University Hospital of Ioannina, Ioannina, GreeceAnna Goussia, Department of Pathology, University Hospital of Ioannina, Ioannina, GreeceSpyridon Voulgaris, Department of Neurosurgery, University Hospital of Ioannina, Ioannina, GreeceAndreas D. Fotopoulos, Department of Nuclear Medicine, University Hospital of Ioannina, Ioannina, GreeceGeorge Fotakopoulos, Department of Neurosurgery, University Hospital of Ioannina, Ioannina, GreeceAntigoni Ntoulia, Department of Pathology, University Hospital of Ioannina, Ioannina, GreeceA...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5638075</comments>
            <pubDate>Wed, 25 Jan 2012 18:14:31 +0100</pubDate>
            <guid isPermaLink="false">5638075</guid>        </item>
        <item>
            <title>A phase II trial of erlotinib in patients with EGFR wild-type advanced non-small-cell lung cancer</title>
            <link>http://www.medworm.com/index.php?rid=5647041&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fb483608628253g17%2F</link>
            <description>Conclusion&amp;nbsp;&amp;nbsp;Erlotinib might be an alternative option for patients resistant to cytotoxic chemotherapy even in those with EGFR wild-type
 NSCLC.
 
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-6DOI 10.1007/s00280-012-1831-0Authors
		Takashi Kobayashi, Comprehensive Cancer Center, Division of Clinical Oncology, Shinshu University School of Medicine, Shinshu University Hospital, 3-1-1, Asahi Matsumoto, Matsumoto, 390-8621 JapanTomonobu Koizumi, Comprehensive Cancer Center, Division of Clinical Oncology, Shinshu University School of Medicine, Shinshu University Hospital, 3-1-1, Asahi Matsumoto, Matsumoto, 390-8621 JapanToshihide Agatsuma, First Department of Internal Medicine, Shinshu University School of Medicine, Matsumoto, JapanMasanori Yasuo, First Departmen...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5647041</comments>
            <pubDate>Wed, 25 Jan 2012 18:14:30 +0100</pubDate>
            <guid isPermaLink="false">5647041</guid>        </item>
        <item>
            <title>The efficacy and safety of melatonin in concurrent chemotherapy or radiotherapy for solid tumors: a meta-analysis of randomized controlled trials</title>
            <link>http://www.medworm.com/index.php?rid=5638076&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F3j88215652332760%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;Melatonin as an adjuvant therapy for cancer led to substantial improvements in tumor remission, 1-year survival, and alleviation
 of radiochemotherapy-related side effects.
 
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-8DOI 10.1007/s00280-012-1828-8Authors
		Ye-min Wang, Department of Pharmacy, The First Affiliated Hospital of Xinxiang Medical University, 88 Jiankang Road, The City of Weihui, Xinxiang, Henan Province, ChinaBao-zhe Jin, Department of Surgery, The First Affiliated Hospital of Xinxiang Medical University, 88 Jiankang Road, The City of Weihui, Xinxiang, Henan Province, ChinaFang Ai, Department of Surgery, The First Affiliated Hospital of Xinxiang Medical University, 88 Jiankang Road, The City of Weihui, Xinxiang, Henan Province, C...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5638076</comments>
            <pubDate>Tue, 24 Jan 2012 06:48:04 +0100</pubDate>
            <guid isPermaLink="false">5638076</guid>        </item>
        <item>
            <title>Clinical pharmacology of trastuzumab emtansine (T-DM1): an antibody–drug conjugate in development for the treatment of HER2-positive cancer</title>
            <link>http://www.medworm.com/index.php?rid=5638077&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fj5n2v3236h5707nm%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;The PK profile of single-agent T-DM1 (3.6&amp;nbsp;mg/kg q3w) is predictable, well characterized, and unaffected by circulating levels
 of HER2 extracellular domain or residual trastuzumab. T-DM1 exposure does not correlate with clinical responses or key adverse
 events.
 
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-12DOI 10.1007/s00280-011-1817-3Authors
		Sandhya Girish, Genentech, Inc, 1 DNA Way, South San Francisco, CA 94080, USAManish Gupta, Genentech, Inc, 1 DNA Way, South San Francisco, CA 94080, USABei Wang, Genentech, Inc, 1 DNA Way, South San Francisco, CA 94080, USADan Lu, Genentech, Inc, 1 DNA Way, South San Francisco, CA 94080, USAIan E. Krop, Dana-Farber Cancer Institute, Boston, MA, USACharles L. Vogel, Sylvester Comprehensive Cancer...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5638077</comments>
            <pubDate>Tue, 24 Jan 2012 06:48:02 +0100</pubDate>
            <guid isPermaLink="false">5638077</guid>        </item>
        <item>
            <title>Prospective evaluation of the drug-metabolizing enzyme polymorphisms and toxicity profile of docetaxel in Korean patients with operable lymph node-positive breast cancer receiving adjuvant chemotherapy</title>
            <link>http://www.medworm.com/index.php?rid=5638078&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fh53387686417pk76%2F</link>
            <description>Discussion&amp;nbsp;&amp;nbsp;Although ABCB1 3435 T/T was significantly associated with docetaxel-related neutropenia in our study population, polymorphism
 of pharmacogenetic genes related to docetaxel metabolism did not appear to be evidently associated with docetaxel-related
 adverse events.
 
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-7DOI 10.1007/s00280-011-1816-4Authors
		Kyu-pyo Kim, Department of Oncology, Asan Medical Center, University of Ulsan College of Medicine, 88, Olympic-ro 43-gil, Poongnap-dong, Songpa-gu, Seoul, 138-736 KoreaJin-Hee Ahn, Department of Oncology, Asan Medical Center, University of Ulsan College of Medicine, 88, Olympic-ro 43-gil, Poongnap-dong, Songpa-gu, Seoul, 138-736 KoreaSung-Bae Kim, Department of Oncology, Asan Medical Center, Univers...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5638078</comments>
            <pubDate>Tue, 24 Jan 2012 06:48:00 +0100</pubDate>
            <guid isPermaLink="false">5638078</guid>        </item>
        <item>
            <title>Correlation between low-level expression of the tumor suppressor gene TAp73 and the chemoresistance of human glioma stem cells</title>
            <link>http://www.medworm.com/index.php?rid=5619682&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fa987336264622870%2F</link>
            <description>Conclusion&amp;nbsp;&amp;nbsp;These findings indicate that TAp73 silencing is hallmark of GSC to maintain their chemoresistance phenotype. Thus, targeting
 TAp73 may provide a novel strategy to eradicating GSCs.
 
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-8DOI 10.1007/s00280-012-1823-0Authors
		Xiaogang Hu, Department of Pharmacy, Southwest Hospital, Third Military Medical University, Chongqing, 400038 ChinaNan Wu, Department of Neurosurgery, Southwest Hospital, Third Military Medical University, Chongqing, 400038 ChinaPeiyuan Xia, Department of Pharmacy, Southwest Hospital, Third Military Medical University, Chongqing, 400038 ChinaSicang Yu, Institute of Pathology, Southwest Hospital, Third Military Medical University, Chongqing, 400038 ChinaFengjun Sun, Department of Ph...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5619682</comments>
            <pubDate>Thu, 19 Jan 2012 06:53:40 +0100</pubDate>
            <guid isPermaLink="false">5619682</guid>        </item>
        <item>
            <title>Randomized phase II study of gemcitabine and S-1 combination versus gemcitabine alone in the treatment of unresectable advanced pancreatic cancer (Japan Clinical Cancer Research Organization PC-01 study)</title>
            <link>http://www.medworm.com/index.php?rid=5619683&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fh89261n507k20h03%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;The GS group showed stronger anticancer activity than the G group, suggesting the need for a large randomized phase III study
 to confirm GS advantages in a specific subset.
 
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-8DOI 10.1007/s00280-012-1822-1Authors
		Masato Ozaka, Department of Gastroenterology, Cancer Institute Hospital, 3-8-31 Ariake, Koto-ku, Tokyo, 135-8550 JapanYuji Matsumura, Department of Gastroenterology, Juntendo University School of Medicine, 2-1-1 Hongo, Bunkyo-ku, Tokyo, 113-8421 JapanHiroshi Ishii, Department of Gastroenterology, Cancer Institute Hospital, 3-8-31 Ariake, Koto-ku, Tokyo, 135-8550 JapanYasushi Omuro, Department of Chemotherapy, Tokyo Metropolitan Cancer and Infectious Diseases Center, Komagome Hospital, 3-1...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5619683</comments>
            <pubDate>Tue, 17 Jan 2012 07:12:28 +0100</pubDate>
            <guid isPermaLink="false">5619683</guid>        </item>
        <item>
            <title>The effect of aprepitant and race on the pharmacokinetics of cyclophosphamide in breast cancer patients</title>
            <link>http://www.medworm.com/index.php?rid=5608149&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fn5w250937238w45k%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;Aprepitant altered the exposure of cyclophosphamide and DCE but not the active 4-OH metabolite, making it unlikely that aprepitant
 would change the clinical efficacy of cyclophosphamide. African Americans were also found to have altered PK compared with
 Caucasian patients.
 
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-8DOI 10.1007/s00280-011-1815-5Authors
		Christine M. Walko, UNC Eshelman School of Pharmacy, University of North Carolina, Chapel Hill, NC, USAAustin J. Combest, UNC Eshelman School of Pharmacy, University of North Carolina, Chapel Hill, NC, USAIvan Spasojevic, Duke Cancer Institute Clinical Pharmacology Laboratory, Duke University Medical Center, Durham, NC, USAAngela Y. C. Yu, UNC Eshelman School of Pharmacy, University of No...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5608149</comments>
            <pubDate>Sat, 14 Jan 2012 16:42:36 +0100</pubDate>
            <guid isPermaLink="false">5608149</guid>        </item>
        <item>
            <title>Phase I trial of oral S-1 combined with gemcitabine and cisplatin for advanced biliary tract cancer (KHBO1002)</title>
            <link>http://www.medworm.com/index.php?rid=5596941&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F5732v60u71t75718%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;We determined the RD of gemcitabine/cisplatin/S-1 combination therapy for advanced biliary tract cancer; we are proceeding
 to a phase II study to investigate the efficacy of this combination therapy for advanced biliary tract cancer.
 
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-8DOI 10.1007/s00280-011-1818-2Authors
		Masashi Kanai, Outpatient Oncology Unit, Kyoto University Hospital, Kyoto, JapanEtsuro Hatano, Department of Surgery, Graduate School of Medicine, Kyoto University Hospital, Kyoto, JapanSyogo Kobayashi, Department of Surgery, Graduate School of Medicine, Osaka University, Osaka, JapanYutaka Fujiwara, Department of Medical Oncology and Hematology, Kobe University Graduate School of Medicine, Kobe, JapanDaisuke Sakai, Department o...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5596941</comments>
            <pubDate>Wed, 11 Jan 2012 17:51:05 +0100</pubDate>
            <guid isPermaLink="false">5596941</guid>        </item>
        <item>
            <title>Ugt1a is required for the protective effect of selenium against irinotecan-induced toxicity</title>
            <link>http://www.medworm.com/index.php?rid=5596942&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fl898722l7m163547%2F</link>
            <description>Conclusion&amp;nbsp;&amp;nbsp;These data support the hypothesis that expression of UGT1A is critical for 5-methylselenocysteine to exert its protective effect against irinotecan-induced toxicity.
 
 
 
 
	Content Type Journal ArticleCategory Short CommunicationPages 1-5DOI 10.1007/s00280-011-1820-8Authors
		Shousong Cao, Department of Cancer Biology, Roswell Park Cancer Institute, Elm and Carlton Streets, Buffalo, NY 14263, USAFarukh A. Durrani, Department of Cancer Biology, Roswell Park Cancer Institute, Elm and Carlton Streets, Buffalo, NY 14263, USAYoucef M. Rustum, Department of Cancer Biology, Roswell Park Cancer Institute, Elm and Carlton Streets, Buffalo, NY 14263, USAY. Eugene Yu, Department of Cancer Genetics, Center for Genetics and Pharmacology, Roswell Park Cancer Institute, Elm and Ca...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5596942</comments>
            <pubDate>Wed, 11 Jan 2012 17:51:03 +0100</pubDate>
            <guid isPermaLink="false">5596942</guid>        </item>
        <item>
            <title>Phase I and pharmacologic study of weekly amrubicin in patients with refractory or relapsed lung cancer: Central Japan Lung Study Group (CJLSG) 0601 trial</title>
            <link>http://www.medworm.com/index.php?rid=5596944&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fk4311p45848557j9%2F</link>
            <description>Conclusion&amp;nbsp;&amp;nbsp;In the present phase I study of AMR administered weekly to previously treated lung cancer patients, the maximum tolerated
 dose and RD were 65 and 60&amp;nbsp;mg/m2, respectively. The best response rate was 15.4%, and adverse events with this schedule were tolerable.
 
 
 
 
	Content Type Journal ArticleCategory Clinical Trial ReportPages 1-7DOI 10.1007/s00280-011-1812-8Authors
		Chiyoe Kitagawa, Department of Medical Oncology, National Hospital Organization Nagoya Medical Center, 4-1-1 Sannomaru, Naka-ku, Nagoya, Aichi, 460-0001 JapanHideo Saka, Department of Medical Oncology, National Hospital Organization Nagoya Medical Center, 4-1-1 Sannomaru, Naka-ku, Nagoya, Aichi, 460-0001 JapanShigehisa Kajikawa, Department of Respiratory Medicine, Nagoya University Graduate Schoo...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5596944</comments>
            <pubDate>Wed, 11 Jan 2012 17:51:02 +0100</pubDate>
            <guid isPermaLink="false">5596944</guid>        </item>
        <item>
            <title>Inhibition of Csn3 expression induces growth arrest and apoptosis of hepatocellular carcinoma cells</title>
            <link>http://www.medworm.com/index.php?rid=5596943&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fu05x73m106124178%2F</link>
            <description>Conclusion&amp;nbsp;&amp;nbsp;Collectively, this study demonstrates Csn3 as an oncogene that regulates the tumorigenesis process in HCC cells.
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-8DOI 10.1007/s00280-011-1810-xAuthors
		Yong-sheng Yu, Department of Infectious Diseases, Sixth People’s Hospital, Shanghai Jiaotong University, Yishan Road 600, Shanghai, 200233 ChinaZheng-hao Tang, Department of Infectious Diseases, Sixth People’s Hospital, Shanghai Jiaotong University, Yishan Road 600, Shanghai, 200233 ChinaQing-chun Pan, Department of Infectious Diseases, Sixth People’s Hospital, Shanghai Jiaotong University, Yishan Road 600, Shanghai, 200233 ChinaXiao-hua Chen, Department of Infectious Diseases, Sixth People’s Hospital, Shanghai Jiaotong University, Yishan Road...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5596943</comments>
            <pubDate>Wed, 11 Jan 2012 17:51:02 +0100</pubDate>
            <guid isPermaLink="false">5596943</guid>        </item>
        <item>
            <title>Analysis of the pharmacodynamic activity of the mTOR inhibitor ridaforolimus (AP23573, MK-8669) in a phase 1 clinical trial</title>
            <link>http://www.medworm.com/index.php?rid=5596945&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fy241g406n1p78439%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;Ridaforolimus was shown to inhibit its intended target, mTOR, in PBMCs, skin, and tumors. In PBMCs and skin, inhibition was
 observed at all dose levels tested, thus supporting but not driving the selection of a recommended phase 2 dose.
 
 
 
 
	Content Type Journal ArticleCategory Clinical Trial ReportPages 1-9DOI 10.1007/s00280-011-1813-7Authors
		Lori Berk, ARIAD Pharmaceuticals, Inc., 26 Landsdowne Street, Cambridge, MA 02139, USAMonica M. Mita, Cancer Therapy and Research Center, Institute for Drug Development, The University of Texas Health Science Center, San Antonio, TX, USAJeff Kreisberg, Cancer Therapy and Research Center, Institute for Drug Development, The University of Texas Health Science Center, San Antonio, TX, USACamille L. Bedrosian, ARIAD Pharmace...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5596945</comments>
            <pubDate>Mon, 09 Jan 2012 19:37:50 +0100</pubDate>
            <guid isPermaLink="false">5596945</guid>        </item>
        <item>
            <title>Addition of rituximab to reduced-dose CHOP chemotherapy is feasible for elderly patients with diffuse large B-cell lymphoma</title>
            <link>http://www.medworm.com/index.php?rid=5571957&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fyu331u7j89042q40%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;RD-RCHOP chemotherapy is well tolerated and effective in elderly patients with DLBCL.
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-8DOI 10.1007/s00280-011-1814-6Authors
		Ho-Jin Shin, Division of Hematology-Oncology, Department of Internal Medicine, School of Medicine, Medical Research Institute, Pusan National University Hospital, 1-10, Ami-Dong, Seo-Gu, Busan, KoreaJoo Seop Chung, Division of Hematology-Oncology, Department of Internal Medicine, School of Medicine, Medical Research Institute, Pusan National University Hospital, 1-10, Ami-Dong, Seo-Gu, Busan, KoreaMoo-Kon Song, Division of Hematology-Oncology, Department of Internal Medicine, School of Medicine, Medical Research Institute, Pusan National University Hospital, 1-10, Ami-Dong, Se...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5571957</comments>
            <pubDate>Wed, 04 Jan 2012 06:59:55 +0100</pubDate>
            <guid isPermaLink="false">5571957</guid>        </item>
        <item>
            <title>Mass balance, excretion and metabolism of [14C] ASA404 in cancer patients in a phase I trial</title>
            <link>http://www.medworm.com/index.php?rid=5571958&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ft04x85360162n5l2%2F</link>
            <description>Conclusion&amp;nbsp;&amp;nbsp;This study defined the substantial excretion of ASA404, mainly as metabolites, in both urine (over half of the dose) and faeces
 (about one-third of the dose) after intravenous administration. Two novel metabolites were identified that were not reported
 by previous studies using nonradioactive techniques.
 
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-10DOI 10.1007/s00280-011-1809-3Authors
		M. J. McKeage, Cancer Clinical Pharmacology Research Group, Auckland Cancer Society Research Centre, School of Medical Sciences, Faculty of Medical and Health Sciences, The University of Auckland, 85 Park Road, Grafton, Auckland, 1142 New ZealandP. C. Fong, Cancer Clinical Pharmacology Research Group, Auckland Cancer Society Research Centre, School of Medic...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5571958</comments>
            <pubDate>Mon, 02 Jan 2012 16:46:11 +0100</pubDate>
            <guid isPermaLink="false">5571958</guid>        </item>
        <item>
            <title>Population pharmacokinetics of cytarabine, etoposide, and daunorubicin in the treatment for acute myeloid leukemia</title>
            <link>http://www.medworm.com/index.php?rid=5571959&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F23889u8k71046577%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;Population-based models characterized the PK for all three drugs. bWBC was a significant covariate for etoposide and cytarabine
 and showed a trend for daunorubicin. Linking the significant bWBC relationships and the relationship between kidney function
 and etoposide clearance to clinical end points would support dose individualization. Patients with above-normal creatinine
 clearances and high bWBC may receive sub-optimal treatment due to elevated etoposide clearances.
 
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-9DOI 10.1007/s00280-011-1800-zAuthors
		Mikkel Krogh-Madsen, Department of Pharmacology and Pharmacotherapy, Faculty of Pharmaceutical Sciences, University of Copenhagen, Jagtvej 160, 2100 Copenhagen, DenmarkBrendan Bender, Departm...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5571959</comments>
            <pubDate>Mon, 02 Jan 2012 16:46:10 +0100</pubDate>
            <guid isPermaLink="false">5571959</guid>        </item>
        <item>
            <title>Exposure–response relationship of AMG 386 in combination with weekly paclitaxel in recurrent ovarian cancer and its implication for dose selection</title>
            <link>http://www.medworm.com/index.php?rid=5559433&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fa7h803343k003161%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;Increased exposure to AMG 386 was associated with improved clinical outcomes in recurrent ovarian cancer, supporting the evaluation
 of a higher dose in future studies.
 
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-10DOI 10.1007/s00280-011-1787-5Authors
		Jian-Feng Lu, Amgen Inc., One Amgen Center Drive, Mailstop 28-3-B, Thousand Oaks, CA 91320, USAErik Rasmussen, Amgen Inc., One Amgen Center Drive, Mailstop 28-3-B, Thousand Oaks, CA 91320, USABeth Y. Karlan, Cedars-Sinai Medical Center, 8700 Beverly Blvd., Los Angeles, CA 90048, USAIgnace B. Vergote, Department of Obstetrics and Gynecology, University Hospital Leuven, Herestraat 49, 3000 Leuven, BelgiumLynn Navale, Amgen Inc., One Amgen Center Drive, Mailstop 28-3-B, Thousand Oaks, CA 91320, ...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5559433</comments>
            <pubDate>Sat, 31 Dec 2011 06:37:17 +0100</pubDate>
            <guid isPermaLink="false">5559433</guid>        </item>
        <item>
            <title>A phase I study for adjuvant chemotherapy of gemcitabine plus S-1 in curatively resected patients with biliary tract cancer: adjusting the dose of adjuvant chemotherapy according to the surgical procedures</title>
            <link>http://www.medworm.com/index.php?rid=5559434&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fc801l55pg115vu16%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;The pharmacokinetics of GEM and S-1 indicate that changing the dose of adjuvant chemotherapy based on the operation method
 for biliary cancers is reasonable. We believe that this regimen will be established as an effective adjuvant chemotherapy
 for biliary cancer in the future.
 
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-7DOI 10.1007/s00280-011-1805-7Authors
		Takeshi Takahara, Department of Surgery, Iwate Medical University School of Medicine, 19-1 Uchimaru, Morioka, Iwate 020-8505, JapanHiroyuki Nitta, Department of Surgery, Iwate Medical University School of Medicine, 19-1 Uchimaru, Morioka, Iwate 020-8505, JapanYasushi Hasegawa, Department of Surgery, Iwate Medical University School of Medicine, 19-1 Uchimaru, Morioka, Iwate 020-8505, ...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5559434</comments>
            <pubDate>Fri, 30 Dec 2011 07:10:07 +0100</pubDate>
            <guid isPermaLink="false">5559434</guid>        </item>
        <item>
            <title>Gene therapy with RNAi targeting UHRF1 driven by tumor-specific promoter inhibits tumor growth and enhances the sensitivity of chemotherapeutic drug in breast cancer in vitro and in vivo</title>
            <link>http://www.medworm.com/index.php?rid=5552028&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fd762020687253644%2F</link>
            <description>In this study, we explored whether UHRF1 can be a therapeutic target for human
 breast carcinoma. We successfully constructed the tumor-specific shRNA expression vector driven by survivin promoter targeting
 UHRF1 gene. The tumor-specific RNA interference system efficiently and specifically knocked down UHRF1 expression, induced
 the apoptosis of tumor cells, and enhanced chemosensitivity of tumor cells to cisplatinum, but not in normal cells in vitro
 and in vivo. Therefore, the survivin promoter-driving shRNA expression system targeting UHRF1 may play a vital and potential
 role for the treatment of specificity and high efficacy in human breast carcinomas.
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-9DOI 10.1007/s00280-011-1801-yAuthors
		Lin Fang, Department of Cli...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5552028</comments>
            <pubDate>Wed, 28 Dec 2011 16:45:19 +0100</pubDate>
            <guid isPermaLink="false">5552028</guid>        </item>
        <item>
            <title>Age-stratified phase I trial of a combination of bortezomib, gemcitabine, and liposomal doxorubicin in patients with advanced malignancies</title>
            <link>http://www.medworm.com/index.php?rid=5552027&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fm62559374605qqm8%2F</link>
            <description>Conclusion&amp;nbsp;&amp;nbsp;Combination of bortezomib, gemcitabine, and liposomal doxorubicin is well tolerated, but with a lower recommended phase II
 dose in elderly patients, and demonstrated antitumor activity, especially in T-cell and small cell histology malignancies.
 
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-10DOI 10.1007/s00280-011-1808-4Authors
		G. S. Falchook, Division of Cancer Medicine, Department of Investigational Cancer Therapeutics (Phase I Clinical Trials Program)-Unit 455, The University of Texas MD Anderson Cancer Center, 1515 Holcombe Boulevard, Houston, TX 77030, USAM. Duvic, Division of Internal Medicine, Department of Dermatology, The University of Texas MD Anderson Cancer Center, 1515 Holcombe Boulevard, Houston, TX 77030, USAD. S. Hong, Divis...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5552027</comments>
            <pubDate>Wed, 28 Dec 2011 16:45:19 +0100</pubDate>
            <guid isPermaLink="false">5552027</guid>        </item>
        <item>
            <title>Preclinical pharmacokinetics of MFGR1877A, a human monoclonal antibody to FGFR3, and prediction of its efficacious clinical dose for the treatment of t(4;14)-positive multiple myeloma</title>
            <link>http://www.medworm.com/index.php?rid=5552030&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fe48016u43x26t361%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;The predicted non-specific clearance of MFGR1877A in humans is similar to typical human IgG1 antibodies and will be verified
 in a Phase 1 study. The projected human efficacious dose and regimen appear to be achievable in patients.
 
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-8DOI 10.1007/s00280-011-1807-5Authors
		Amrita V. Kamath, Department of Pharmacokinetics and Pharmacodynamics, Genentech, Inc., 1 DNA Way, South San Francisco, CA 94080, USADan Lu, Department of Pharmacokinetics and Pharmacodynamics, Genentech, Inc., 1 DNA Way, South San Francisco, CA 94080, USAPriyanka Gupta, Department of Pharmacokinetics and Pharmacodynamics, Genentech, Inc., 1 DNA Way, South San Francisco, CA 94080, USADenise Jin, Department of Pharmacokinetics and P...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5552030</comments>
            <pubDate>Tue, 27 Dec 2011 16:50:37 +0100</pubDate>
            <guid isPermaLink="false">5552030</guid>        </item>
        <item>
            <title>Preclinical pharmacokinetics of MEHD7945A, a novel EGFR/HER3 dual-action antibody, and prediction of its human pharmacokinetics and efficacious clinical dose</title>
            <link>http://www.medworm.com/index.php?rid=5552029&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fn3440779l2k112q3%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;The PK of MEHD7945A was nonlinear in mouse and monkey in the dose range tested. The nonspecific clearance in monkey was approximately
 twofold higher than typical humanized IgG1 antibodies. The projected human efficacious dose and dose regimen appear to be
 achievable in patients.
 
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-7DOI 10.1007/s00280-011-1806-6Authors
		Amrita V. Kamath, Department of Pharmacokinetics and Pharmacodynamics, Genentech, Inc., South San Francisco, CA 94080, USADan Lu, Department of Pharmacokinetics and Pharmacodynamics, Genentech, Inc., South San Francisco, CA 94080, USAPriyanka Gupta, Department of Pharmacokinetics and Pharmacodynamics, Genentech, Inc., South San Francisco, CA 94080, USADenise Jin, Department of Pharm...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5552029</comments>
            <pubDate>Tue, 27 Dec 2011 16:50:37 +0100</pubDate>
            <guid isPermaLink="false">5552029</guid>        </item>
        <item>
            <title>Afatinib pharmacokinetics and metabolism after oral administration to healthy male volunteers</title>
            <link>http://www.medworm.com/index.php?rid=5552031&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fg02524523un14102%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;Afatinib displayed a complete mass balance with the main route of excretion via feces. Afatinib undergoes minimal metabolism.
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-11DOI 10.1007/s00280-011-1803-9Authors
		Peter Stopfer, Boehringer Ingelheim Pharma GmbH &amp; Co. KG, Birkendorfer Strasse, 88400 Biberach an der Riss, GermanyKristell Marzin, Boehringer Ingelheim Pharma GmbH &amp; Co. KG, Birkendorfer Strasse, 88400 Biberach an der Riss, GermanyHans Narjes, Boehringer Ingelheim Pharma GmbH &amp; Co. KG, Birkendorfer Strasse, 88400 Biberach an der Riss, GermanyDietmar Gansser, Boehringer Ingelheim Pharma GmbH &amp; Co. KG, Birkendorfer Strasse, 88400 Biberach an der Riss, GermanyMehdi Shahidi, Boehringer Ingelheim, Bracknell, UKMartina Uttereuther-Fischer, B...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5552031</comments>
            <pubDate>Mon, 26 Dec 2011 16:44:10 +0100</pubDate>
            <guid isPermaLink="false">5552031</guid>        </item>
        <item>
            <title>Pharmacokinetics of carboplatin in a hemodialysis patient with small-cell lung cancer</title>
            <link>http://www.medworm.com/index.php?rid=5544158&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fx27r48380536k405%2F</link>
            <description>Conclusion&amp;nbsp;&amp;nbsp;Based on the results of this study, a value close to the targeted AUC can be obtained in a hemodialysis patient with cancer
 when carboplatin is administered at a dose determined based on the Calvert formula. These results may be useful to achieve
 a targeted AUC in hemodialysis patients. A certain amount of carboplatin can be eliminated by performing hemodialysis in an
 early phase when protein binding ratio is low after transition to the elimination phase to enable stable the concentration.
 
 
 
 
	Content Type Journal ArticleCategory Short CommunicationPages 1-4DOI 10.1007/s00280-011-1802-xAuthors
		Mikako Hiraike, Department of Pharmacy, National Hospital Organization Kumamoto Medical Center, 1-5 Ninomaru, Kumamoto, Kumamoto 860-0008, JapanYoichi Hiraki, Departme...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5544158</comments>
            <pubDate>Thu, 22 Dec 2011 12:50:07 +0100</pubDate>
            <guid isPermaLink="false">5544158</guid>        </item>
        <item>
            <title>Anti-tumor activity and mechanism of action for a cyanoaziridine-derivative, AMP423</title>
            <link>http://www.medworm.com/index.php?rid=5537462&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fw073x32217384x72%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;AMP423 has pro-oxidant effects similar to imexon, has greater cytotoxic potency in vitro, and has anti-tumor activity in hematologic
 tumors in vivo.
 
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-11DOI 10.1007/s00280-011-1784-8Authors
		Robert T. Dorr, The University of Arizona Cancer Center, College of Medicine, 1515 N. Campbell Avenue, Tucson, AZ 85724-5024, USALee Wisner, The University of Arizona Cancer Center, College of Medicine, 1515 N. Campbell Avenue, Tucson, AZ 85724-5024, USABetty K. Samulitis, The University of Arizona Cancer Center, College of Medicine, 1515 N. Campbell Avenue, Tucson, AZ 85724-5024, USATerry H. Landowski, The University of Arizona Cancer Center, College of Medicine, 1515 N. Campbell Avenue, Tucson, AZ 85724-5...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5537462</comments>
            <pubDate>Tue, 20 Dec 2011 16:47:30 +0100</pubDate>
            <guid isPermaLink="false">5537462</guid>        </item>
        <item>
            <title>CIP-13F, a novel aminopeptidase N (APN/CD13) inhibitor, inhibits Lewis lung carcinoma growth and metastasis in mice</title>
            <link>http://www.medworm.com/index.php?rid=5537461&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fe1281n456558j559%2F</link>
            <description>Conclusion&amp;nbsp;&amp;nbsp;Our results showed that CIP-13F effectively inhibited LLC growth and pulmonary metastasis in mice and suggested that CIP-13F
 is a potential drug for the treatment for cancers with positive APN/CD13 expression.
 
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-10DOI 10.1007/s00280-011-1799-1Authors
		Ke-Ling Pei, Key Laboratory for Rare Disease of Shandong Province, Department of Pharmacology, Institute of Materia Medica, Shandong Academy of Medical Sciences, Jinan, 250062 ChinaYi Yuan, Department of Pharmacology, School of Pharmaceutical Sciences, Shandong University, Jinan, 250012 ChinaSan-Hai Qin, Key Laboratory for Rare Disease of Shandong Province, Department of Pharmacology, Institute of Materia Medica, Shandong Academy of Medical Sciences, J...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5537461</comments>
            <pubDate>Tue, 20 Dec 2011 16:47:30 +0100</pubDate>
            <guid isPermaLink="false">5537461</guid>        </item>
        <item>
            <title>Tolerability and pharmacokinetic profile of a sunitinib powder formulation in pediatric patients with refractory solid tumors: a Children’s Oncology Group study</title>
            <link>http://www.medworm.com/index.php?rid=5524121&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Flh4282456qw34535%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;The pharmacokinetic profile of sunitinib appears similar between a powder formulation and published data using capsules. The
 powder formulation allows patients unable to swallow capsules to receive sunitinib.
 
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-7DOI 10.1007/s00280-011-1798-2Authors
		Steven G. DuBois, Department of Pediatrics, UCSF School of Medicine, 505 Parnassus Avenue, M646, San Francisco, CA 94143-0106, USASuzanne Shusterman, Department of Pediatrics, Dana-Farber Cancer Institute, Children’s Hospital Boston, Harvard Medical School, Boston, MA, USAJoel M. Reid, Department of Pharmacology, Mayo College of Medicine, Rochester, MN, USAAshish M. Ingle, Children’s Oncology Group Operations Center, Arcadia, CA, USACharlotte H. Ahe...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5524121</comments>
            <pubDate>Sat, 17 Dec 2011 16:43:43 +0100</pubDate>
            <guid isPermaLink="false">5524121</guid>        </item>
        <item>
            <title>A phase I dose-escalation and pharmacokinetic study of enzastaurin and erlotinib in patients with advanced solid tumors</title>
            <link>http://www.medworm.com/index.php?rid=5494595&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fe972267188417777%2F</link>
            <description>Conclusion&amp;nbsp;&amp;nbsp;The combination of enzastaurin 500&amp;nbsp;mg daily and erlotinib 150&amp;nbsp;mg daily is well tolerated and does not alter the pharmacokinetics
 of the individual drugs, with clinical activity seen. A phase II trial of this combination has been initiated in patients
 with advanced-stage NSCLC.
 
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-8DOI 10.1007/s00280-011-1792-8Authors
		Sukhmani K. Padda, Department of Medicine, Division of Oncology, Stanford University, 875 Blake Wilbur Drive, Stanford, CA 94305-5826, USAYelena Krupitskaya, Department of Medicine, Division of Oncology, Stanford University, 875 Blake Wilbur Drive, Stanford, CA 94305-5826, USALaveena Chhatwani, Department of Medicine, Division of Oncology, Stanford University, 875 Blake Wilbu...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5494595</comments>
            <pubDate>Sat, 10 Dec 2011 16:55:07 +0100</pubDate>
            <guid isPermaLink="false">5494595</guid>        </item>
        <item>
            <title>Phase II study of S-1 monotherapy in patients with previously treated, advanced non-small-cell lung cancer</title>
            <link>http://www.medworm.com/index.php?rid=5486437&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fv6062230088856q1%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;S-1 monotherapy is effective and well-tolerated treatment for previously treated advanced NSCLC.
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-7DOI 10.1007/s00280-011-1795-5Authors
		M. Wada, Department of Respiratory Medicine, Kitasato University School of Medicine, 1-15-1 Kitasato Minami-ku, Sagamihara, Kanagawa 252-0374, JapanM. Yamamoto, Department of Respiratory Medicine, Kitasato University School of Medicine, 1-15-1 Kitasato Minami-ku, Sagamihara, Kanagawa 252-0374, JapanS. Ryuge, Department of Respiratory Medicine, Kitasato University School of Medicine, 1-15-1 Kitasato Minami-ku, Sagamihara, Kanagawa 252-0374, JapanY. Nagashima, Department of Respiratory Medicine, Kitasato University School of Medicine, 1-15-1 Kitasato Minami-ku, Sagami...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5486437</comments>
            <pubDate>Wed, 07 Dec 2011 12:54:49 +0100</pubDate>
            <guid isPermaLink="false">5486437</guid>        </item>
        <item>
            <title>Influence of H2-receptor antagonists and proton pump inhibitors on dasatinib pharmacokinetics in Japanese leukemia patients</title>
            <link>http://www.medworm.com/index.php?rid=5486438&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fb851028x660577w5%2F</link>
            <description>Conclusion&amp;nbsp;&amp;nbsp;Clinicians should be aware that administration of an acid suppressant such as famotidine, nizatidine, and lansoprazole can
 decrease the absorption of dasatinib from the gastrointestinal tract, thereby resulting in a significant decrease in the plasma
 concentration of dasatinib. The combination of dasatinib and an acid suppressant requires careful therapeutic drug monitoring
 of the dasatinib plasma concentration to ensure effective patient exposure to the drug.
 
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-6DOI 10.1007/s00280-011-1797-3Authors
		Naoto Takahashi, Department of Hematology, Nephrology, and Rheumatology, Akita University Graduate School of Medicine, Akita, JapanMasatomo Miura, Department of Pharmacy, Akita University Hospital, 1-...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5486438</comments>
            <pubDate>Tue, 06 Dec 2011 17:01:19 +0100</pubDate>
            <guid isPermaLink="false">5486438</guid>        </item>
        <item>
            <title>Going past the data for temozolomide</title>
            <link>http://www.medworm.com/index.php?rid=5486439&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ft71r063086021823%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The benefit of six cycles of adjuvant temozolomide was documented in a randomized phase III (EORTC-NCIC CE.3) trial, and this
 therapy, following combined temozolomide and radiation, is the standard of care for patients with newly diagnosed glioblastoma.
 We comment on the differences in the length of adjuvant therapy in both clinical practice and national studies (e.g. RTOG
 0825), usually doubling the length in the EORTC/NCIC study, and relate to historic adjuvant trials for solid tumors.
 
 
	Content Type Journal ArticleCategory CommentaryPages 1-3DOI 10.1007/s00280-011-1796-4Authors
		J. Lee Villano, Department of Medicine, Section of Hematology/Oncology, University of Illinois at Chicago, 840 S. Wood St. Rm. 839 (M/C 713), Chicago, IL 60612, USANathalie Letarte, Fa...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5486439</comments>
            <pubDate>Tue, 06 Dec 2011 17:01:18 +0100</pubDate>
            <guid isPermaLink="false">5486439</guid>        </item>
        <item>
            <title>The effect of dacomitinib (PF-00299804) on CYP2D6 activity in healthy volunteers who are extensive or intermediate metabolizers</title>
            <link>http://www.medworm.com/index.php?rid=5486440&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fr37jm620725342t7%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;Single-dose administration of dacomitinib plus DM was safe and well tolerated in HVs and resulted in a significant increase
 in systemic exposures of DM in extensive metabolizers. No effect was observed on the pharmacokinetics of dacomitinib. Drug–drug
 interaction may occur when dacomitinib is concomitantly administered with therapeutic agents metabolized by cytochrome P450
 (CYP) 2D6. Administration of drugs which are highly dependent on CYP2D6 metabolism may require dose adjustment, or substitution
 with an alternative medication.
 
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-7DOI 10.1007/s00280-011-1793-7Authors
		Carlo L. Bello, Pfizer Oncology, 235 East 42nd Street, New York, NY 10017, USARobert R. LaBadie, Pfizer PharmaTherapeutics, N...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5486440</comments>
            <pubDate>Tue, 06 Dec 2011 17:01:16 +0100</pubDate>
            <guid isPermaLink="false">5486440</guid>        </item>
        <item>
            <title>Phase I study for ridaforolimus, an oral mTOR inhibitor, in Japanese patients with advanced solid tumors</title>
            <link>http://www.medworm.com/index.php?rid=5486442&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ff067803550817367%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;Ridaforolimus was well tolerated up to a dose of 40&amp;nbsp;mg in Japanese patients. Preliminary evidence of antitumor activity was
 observed for patients with solid tumors. Further investigation at this dose is warranted.
 
 
 
 
	Content Type Journal ArticleCategory Clinical Trial ReportPages 1-7DOI 10.1007/s00280-011-1788-4Authors
		Yoshitaka Seki, Division of Internal Medicine, National Cancer Center Hospital, Tsukiji 5-1-1, Chuo-ku, Tokyo 104-0045, JapanNoboru Yamamoto, Division of Internal Medicine, National Cancer Center Hospital, Tsukiji 5-1-1, Chuo-ku, Tokyo 104-0045, JapanYosuke Tamura, Division of Internal Medicine, National Cancer Center Hospital, Tsukiji 5-1-1, Chuo-ku, Tokyo 104-0045, JapanYasushi Goto, Division of Internal Medicine, National Cancer Center...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5486442</comments>
            <pubDate>Mon, 05 Dec 2011 17:33:57 +0100</pubDate>
            <guid isPermaLink="false">5486442</guid>        </item>
        <item>
            <title>Treatment of experimental extravasation of amrubicin, liposomal doxorubicin, and mitoxantrone with dexrazoxane</title>
            <link>http://www.medworm.com/index.php?rid=5486441&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fp24589r156153t11%2F</link>
            <description>Abstract
 Purpose&amp;nbsp;&amp;nbsp;Dexrazoxane is an established treatment option in extravasation of the classic anthracyclines such as doxorubicin, epirubicin,
 and daunorubicin. However, it is not known whether the protection against the devastating tissue injuries extends into extravasation
 with new types of anthracyclines, the anthracenediones, or the liposomal pegylated anthracycline formulations. We therefore
 tested the antidotal efficacy of dexrazoxane against extravasation of amrubicin, mitoxantrone, and liposomal pegylated doxorubicin
 in mice.
 
 
 
 
 Methods&amp;nbsp;&amp;nbsp;A total of 80 female B6D2F1 mice were tested in an established mouse extravasation model. The mice had experimental extravasations
 of amrubicin, mitoxtanrone, and Caelyx and were immediately hereafter treated with ...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5486441</comments>
            <pubDate>Mon, 05 Dec 2011 17:33:57 +0100</pubDate>
            <guid isPermaLink="false">5486441</guid>        </item>
        <item>
            <title>Differentiation-inducing factor-1 enhances 5-fluorouracil action on oral cancer cells inhibiting E2F1 and thymidylate synthase mRNAs accumulation</title>
            <link>http://www.medworm.com/index.php?rid=5476154&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F26728215300l15v8%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;These findings suggest a tumor-specific action of DIF-1 on oral carcinoma cells. Thus, interfering with E2F1 and TS transcription,
 DIF-1 potentiates TS enzymatic inhibitors.
 
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-7DOI 10.1007/s00280-011-1790-xAuthors
		Andrea Elio Sprio, Department of Clinical and Biological Sciences, University of Turin, Ospedale San Luigi Gonzaga, 10043 Orbassano, ItalyFederica Di Scipio, Department of Clinical and Biological Sciences, University of Turin, Ospedale San Luigi Gonzaga, 10043 Orbassano, ItalyPaolo Ceppi, Department of Clinical and Biological Sciences, University of Turin, Ospedale San Luigi Gonzaga, 10043 Orbassano, ItalyPaolina Salamone, Department of Clinical and Biological Sciences, University of Tur...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5476154</comments>
            <pubDate>Sat, 03 Dec 2011 16:49:38 +0100</pubDate>
            <guid isPermaLink="false">5476154</guid>        </item>
        <item>
            <title>Intratumor heterogeneity and chemotherapy-induced changes in EGFR status in non-small cell lung cancer</title>
            <link>http://www.medworm.com/index.php?rid=5468411&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F37t3g2013402t828%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;Tumor heterogeneity and probably also previous systemic treatment may be an obstacle for correct interpretation of EGFR status
 in NSCLC. Heterogeneity regarding EGFR mutations is probably rare and previously reported intra and intertumor heterogeneity
 may be due to methodological issues. In the current and future clinical scenario with many different options for systemic
 treatment both as 2nd line and beyond, it is increasingly important to further elucidate the role extent of chemotherapy-induced
 changes in biomarker expression for proper use of biomarkers in order to customize treatment and thus improve prognosis.
 
 
 
 
	Content Type Journal ArticleCategory Mini ReviewPages 1-11DOI 10.1007/s00280-011-1791-9Authors
		Jan Nyrop Jakobsen, Department of Oncology,...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5468411</comments>
            <pubDate>Wed, 30 Nov 2011 18:42:27 +0100</pubDate>
            <guid isPermaLink="false">5468411</guid>        </item>
        <item>
            <title>A phase I trial of docetaxel and pulse-dose 17-allylamino-17-demethoxygeldanamycin in adult patients with solid tumors</title>
            <link>http://www.medworm.com/index.php?rid=5456981&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fk1605g5xu456n137%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;The combination of docetaxel and 17-AAG was well tolerated in adult patients with solid tumors, although patient intolerance
 to the DMSO formulation precluded further dose escalation. The recommended phase II dose is docetaxel 70&amp;nbsp;mg/m2 and 17-AAG 500&amp;nbsp;mg/m2.
 
 
 
 
	Content Type Journal ArticleCategory Clinical Trial ReportPages 1-9DOI 10.1007/s00280-011-1789-3Authors
		Gopa Iyer, Department of Medicine, Memorial Sloan-Kettering Cancer Center, 1275 York Avenue, New York, NY 10021, USAMichael J. Morris, Department of Medicine, Memorial Sloan-Kettering Cancer Center, 1275 York Avenue, New York, NY 10021, USADana Rathkopf, Department of Medicine, Memorial Sloan-Kettering Cancer Center, 1275 York Avenue, New York, NY 10021, USASusan F. Slovin, Department of Me...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5456981</comments>
            <pubDate>Mon, 28 Nov 2011 16:59:35 +0100</pubDate>
            <guid isPermaLink="false">5456981</guid>        </item>
        <item>
            <title>Evaluation of nilotinib in advanced GIST previously treated with imatinib and sunitinib</title>
            <link>http://www.medworm.com/index.php?rid=5456982&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ful5n687327722l30%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;Nilotinib was well tolerated in these patients with advanced GIST. Accrual was halted due to insufficient clinical benefit.
 However, nilotinib may provide benefit to specific subsets of advanced GIST with exon 17 mutations.
 
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-6DOI 10.1007/s00280-011-1785-7Authors
		C. Cauchi, Regina Elena Institute for Cancer Research, Rome, ItalyN. Somaiah, Department of Medical Oncology, Fox Chase Cancer Center, Philadelphia, PA, USAP. F. Engstrom, Department of Medical Oncology, Fox Chase Cancer Center, Philadelphia, PA, USAS. Litwin, Department of Biostatistics, Fox Chase Cancer Center, Philadelphia, PA, USAM. Lopez, Regina Elena Institute for Cancer Research, Rome, ItalyJ. Lee, Protocol Management Office, Fox C...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5456982</comments>
            <pubDate>Sat, 26 Nov 2011 16:48:37 +0100</pubDate>
            <guid isPermaLink="false">5456982</guid>        </item>
        <item>
            <title>Phase I/II study of gemcitabine as a fixed dose rate infusion and S-1 combination therapy (FGS) in gemcitabine-refractory pancreatic cancer patients</title>
            <link>http://www.medworm.com/index.php?rid=5449525&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fm4w3652683j12802%2F</link>
            <description>Conclusion&amp;nbsp;&amp;nbsp;This combination regimen of FGS is active and well tolerated in patients with Gem-refractory PC.
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-8DOI 10.1007/s00280-011-1786-6Authors
		Chigusa Morizane, Division of Hepatobiliary and Pancreatic Oncology, National Cancer Center Hospital, 5-1-1 Tsukiji, Chuo-ku, Tokyo, 104-0045 JapanTakuji Okusaka, Division of Hepatobiliary and Pancreatic Oncology, National Cancer Center Hospital, 5-1-1 Tsukiji, Chuo-ku, Tokyo, 104-0045 JapanHideki Ueno, Division of Hepatobiliary and Pancreatic Oncology, National Cancer Center Hospital, 5-1-1 Tsukiji, Chuo-ku, Tokyo, 104-0045 JapanShunsuke Kondo, Division of Hepatobiliary and Pancreatic Oncology, National Cancer Center Hospital, 5-1-1 Tsukiji, Chuo-ku, Tokyo, 104-0045...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5449525</comments>
            <pubDate>Fri, 25 Nov 2011 17:57:53 +0100</pubDate>
            <guid isPermaLink="false">5449525</guid>        </item>
        <item>
            <title>Increased cellular accumulation and distribution of amrubicin contribute to its activity in anthracycline-resistant cancer cells</title>
            <link>http://www.medworm.com/index.php?rid=5449526&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fv7055k55077g2p81%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;Amrubicin appears to have a distinct mode of action that overcomes typical anthracycline resistance mechanisms. Therefore,
 amrubicin may be useful in the treatment of anthracycline-refractory or anthracycline-resistant tumors.
 
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-12DOI 10.1007/s00280-011-1782-xAuthors
		Vidya Mamidipudi, Translational Development Department, Celgene Corporation, 1500 Owens St. Suite 600, San Francisco, CA 94158, USATao Shi, Celgene Corporation, 4550 Town Centre Court, San Diego, CA 92121, USAHelen Brady, Celgene Corporation, 4550 Town Centre Court, San Diego, CA 92121, USASekhar Surapaneni, Drug Metabolism and Pharmacokinetics Department, Celgene Corporation, 86 Morris Ave., Summit, NJ 07901, USARajesh Chopra, Transl...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5449526</comments>
            <pubDate>Fri, 25 Nov 2011 17:57:52 +0100</pubDate>
            <guid isPermaLink="false">5449526</guid>        </item>
        <item>
            <title>Pharmacokinetic analysis of capecitabine and cisplatin in combination with trastuzumab in Japanese patients with advanced HER2-positive gastric cancer</title>
            <link>http://www.medworm.com/index.php?rid=5449527&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fa1878705159m3845%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;Variability in the AUClast and C
 max values for the capecitabine was consistent with the known PK profile of capecitabine and fell within established limits.
 Concurrent trastuzumab therapy is unlikely to alter the PK or safety profile of capecitabine or cisplatin in Japanese patients
 with HER2-positive AGC.
 
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-7DOI 10.1007/s00280-011-1783-9Authors
		Taroh Satoh, Department of Frontier Science for Cancer and Chemotherapy, Graduate School of Medicine, Osaka University, Osaka, JapanYasushi Omuro, Department of Chemotherapy, Tokyo Metropolitan Cancer and Infectious Diseases Center, Komagome Hospital, Tokyo, JapanYasutsuna Sasaki, Department of Medical Oncology, Saitama International Medical Center–Co...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5449527</comments>
            <pubDate>Thu, 24 Nov 2011 17:45:15 +0100</pubDate>
            <guid isPermaLink="false">5449527</guid>        </item>
        <item>
            <title>Plasma and cerebrospinal fluid pharmacokinetics of thalidomide and lenalidomide in nonhuman primates</title>
            <link>http://www.medworm.com/index.php?rid=5449528&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fd757735883523175%2F</link>
            <description>Conclusion&amp;nbsp;&amp;nbsp;Thalidomide and lenalidomide penetrate into the CSF after oral administration of clinically relevant doses. Plasma exposure
 to lenalidomide was similar in our model to that observed in studies involving children who have brain tumors. These results
 support further development of lenalidomide for the treatment of central nervous system malignancies.
 
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-5DOI 10.1007/s00280-011-1781-yAuthors
		Jodi A. Muscal, Texas Children’s Cancer Center, Baylor College of Medicine, 1102 Bates Street, Suite 1220, Houston, TX 77030, USAYongkai Sun, Celgene Corporation, Summit, NJ, USAJed G. Nuchtern, Department of Surgery, Texas Children’s Hospital, Baylor College of Medicine, Houston, TX, USARobert C. Dauser, Depa...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5449528</comments>
            <pubDate>Wed, 23 Nov 2011 16:39:25 +0100</pubDate>
            <guid isPermaLink="false">5449528</guid>        </item>
        <item>
            <title>A phase I and pharmacokinetic study of oral 3-aminopyridine-2-carboxaldehyde thiosemicarbazone (3-AP, NSC #663249) in the treatment of advanced-stage solid cancers: a California Cancer Consortium Study</title>
            <link>http://www.medworm.com/index.php?rid=5440341&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F2m15m031025702p7%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;Oral 3-AP is well tolerated and has an MTD similar to its intravenous form after accounting for the oral bioavailability.
 Oral 3-AP is associated with a modest clinical benefit rate of 25% in our treated patient population with advanced solid tumors.
 
 
 
 
	Content Type Journal ArticleCategory Clinical Trial ReportPages 1-9DOI 10.1007/s00280-011-1779-5Authors
		Joseph Chao, City of Hope Medical Center, Building room 4117, 1500 East Duarte Road, 91010 Duarte, CA, USATimothy W. Synold, City of Hope Medical Center, Building room 4117, 1500 East Duarte Road, 91010 Duarte, CA, USARobert J. Morgan, City of Hope Medical Center, Building room 4117, 1500 East Duarte Road, 91010 Duarte, CA, USACharles Kunos, Case Western Reserve University, Cleveland, OH, USAJeff Longmate, ...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5440341</comments>
            <pubDate>Mon, 21 Nov 2011 18:09:34 +0100</pubDate>
            <guid isPermaLink="false">5440341</guid>        </item>
        <item>
            <title>Involvement of nitric oxide on the pathogenesis of irinotecan-induced intestinal mucositis: role of cytokines on inducible nitric oxide synthase activation</title>
            <link>http://www.medworm.com/index.php?rid=5440342&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fq603385m251r3668%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;This study suggests a role of nitric oxide in the pathogenesis of irinotecan-induced intestinal mucositis and also provides
 evidence for the participation of cytokines on iNOS induction.
 
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-12DOI 10.1007/s00280-011-1780-zAuthors
		Roberto César P. Lima-Júnior, Department of Physiology and Pharmacology, Faculty of Medicine, Federal University of Ceará, Rua Cel Nunes de Melo, 1315, Rodolfo Teófilo, Fortaleza, Ceará 60430-270, BrazilAline A. Figueiredo, Department of Physiology and Pharmacology, Faculty of Medicine, Federal University of Ceará, Rua Cel Nunes de Melo, 1315, Rodolfo Teófilo, Fortaleza, Ceará 60430-270, BrazilHelano C. Freitas, Department of Physiology and Pharmacology, Faculty of ...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5440342</comments>
            <pubDate>Sat, 19 Nov 2011 16:51:35 +0100</pubDate>
            <guid isPermaLink="false">5440342</guid>        </item>
        <item>
            <title>Predictive value of MGMT, hMLH1, hMSH2 and BRCA1 protein expression for pathological complete response to neoadjuvant chemotherapy in basal-like breast cancer patients</title>
            <link>http://www.medworm.com/index.php?rid=5421609&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fj548955405kgt554%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;MGMT status is a predictive factor for pCR with neoadjuvant anthracycline-based plus taxane combination chemotherapy, which
 may be helpful in the selection of appropriate NACT for Japanese patients with BLBC.
 
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-8DOI 10.1007/s00280-011-1777-7Authors
		Katsuya Nakai, Department of Breast Oncology, Juntendo University School of Medicine, Bunkyo-ku, Tokyo, JapanHiroyuki Mitomi, Department of Human Pathology, Juntendo University School of Medicine, 2-1-1 Hongo, Bunkyo-ku, Tokyo 113-8421, JapanYimit Alkam, Department of Breast Oncology, Juntendo University School of Medicine, Bunkyo-ku, Tokyo, JapanAtsushi Arakawa, Department of Human Pathology, Juntendo University School of Medicine, 2-1-1 Hongo, Bunkyo-...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5421609</comments>
            <pubDate>Mon, 14 Nov 2011 16:53:00 +0100</pubDate>
            <guid isPermaLink="false">5421609</guid>        </item>
        <item>
            <title>Chidamide (CS055/HBI-8000): a new histone deacetylase inhibitor of the benzamide class with antitumor activity and the ability to enhance immune cell-mediated tumor cell cytotoxicity</title>
            <link>http://www.medworm.com/index.php?rid=5407128&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fq465k602k221v6w7%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;The results presented in this study provide evidence that chidamide has potential applicability for the treatment of a variety
 of tumor types, either as a single agent or in combination therapies.
 
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-9DOI 10.1007/s00280-011-1766-xAuthors
		Zhi-Qiang Ning, Chipscreen Biosciences Ltd., Bio-Incubator 2-601, 1st Ave. of Gaoxin Road, Hi-Tech Industrial Park, Shenzhen, 518057 Guangdong, ChinaZhi-Bin Li, Chipscreen Biosciences Ltd., Bio-Incubator 2-601, 1st Ave. of Gaoxin Road, Hi-Tech Industrial Park, Shenzhen, 518057 Guangdong, ChinaMichael J. Newman, HUYA Bioscience International, 12531 High Bluff Drive Suite 138, San Diego, CA 92130, USASong Shan, Chipscreen Biosciences Ltd., Bio-Incubator 2-601, 1st Av...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5407128</comments>
            <pubDate>Fri, 11 Nov 2011 12:48:55 +0100</pubDate>
            <guid isPermaLink="false">5407128</guid>        </item>
        <item>
            <title>A novel multi-targeted tyrosine kinase inhibitor, linifanib (ABT-869), produces functional and structural changes in tumor vasculature in an orthotopic rat glioma model</title>
            <link>http://www.medworm.com/index.php?rid=5407127&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F90034676r9g74535%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Tyrosine kinase inhibitors represent a class of targeted therapy that has proven to be successful for cancer treatment. Linifanib
 is a novel, orally active multi-targeted receptor tyrosine kinase (RTK) inhibitor that exhibits potent antitumor and antiangiogenic
 activities against a broad spectrum of experimental tumors and malignancies in patients. The compound is currently being evaluated
 in phase 2 and 3 clinical trials. To investigate the effectiveness of linifinib against gliomas and the mechanism of drug
 action, we characterized treatment-induced antitumor and antiangiogenic responses to linifanib in an orthotopic rat glioma
 model. The effect of linifanib treatment on tumor growth was determined by tumor volume assessment using anatomical magnetic
 resonance i...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5407127</comments>
            <pubDate>Fri, 11 Nov 2011 12:48:55 +0100</pubDate>
            <guid isPermaLink="false">5407127</guid>        </item>
        <item>
            <title>Phase I study of continuous afatinib (BIBW 2992) in patients with advanced non-small cell lung cancer after prior chemotherapy/erlotinib/gefitinib (LUX-Lung 4)</title>
            <link>http://www.medworm.com/index.php?rid=5407129&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F51672w7002511048%2F</link>
            <description>Conclusion&amp;nbsp;&amp;nbsp;Recommended dose for Phase II was defined as 50&amp;nbsp;mg/day for Japanese patients; the same as for non-Japanese patients.
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-9DOI 10.1007/s00280-011-1738-1Authors
		H. Murakami, Division of Thoracic Oncology, Shizuoka Cancer Center, 1007, Shimonagakubo Nagaizumi-cho Sunto-gun, Shizuoka, 411-8777 JapanT. Tamura, National Cancer Center Hospital, Tokyo, JapanT. Takahashi, Division of Thoracic Oncology, Shizuoka Cancer Center, 1007, Shimonagakubo Nagaizumi-cho Sunto-gun, Shizuoka, 411-8777 JapanH. Nokihara, National Cancer Center Hospital, Tokyo, JapanT. Naito, Division of Thoracic Oncology, Shizuoka Cancer Center, 1007, Shimonagakubo Nagaizumi-cho Sunto-gun, Shizuoka, 411-8777 JapanY. Nakamura, Division of ...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5407129</comments>
            <pubDate>Wed, 09 Nov 2011 17:55:57 +0100</pubDate>
            <guid isPermaLink="false">5407129</guid>        </item>
        <item>
            <title>Sorafenib for hepatocellular carcinoma according to Child-Pugh class of liver function</title>
            <link>http://www.medworm.com/index.php?rid=5407130&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fc3078t0005740q61%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorPages 1-2DOI 10.1007/s00280-011-1776-8Authors
		Fabio Farinati, Department of Surgical and Gastroenterological Sciences, University of Padua, Padua, ItalyAnna Giacomin, Department of Surgical and Gastroenterological Sciences, University of Padua, Padua, ItalyVeronica Vanin, Department of Surgical and Gastroenterological Sciences, University of Padua, Padua, Italy
	

	
		Journal Cancer Chemotherapy and PharmacologyOnline ISSN 1432-0843Print ISSN 0344-5704 (Source: Cancer Chemotherapy and Pharmacology)</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5407130</comments>
            <pubDate>Wed, 09 Nov 2011 17:55:56 +0100</pubDate>
            <guid isPermaLink="false">5407130</guid>        </item>
        <item>
            <title>Feasibility of biweekly combination chemotherapy with capecitabine, irinotecan, and oxaliplatin in patients with metastatic solid tumors: results of a two-step phase I trial: XELIRI and XELIRINOX</title>
            <link>http://www.medworm.com/index.php?rid=5407132&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fb178608275r44v20%2F</link>
            <description>Conclusion&amp;nbsp;&amp;nbsp;XELIRI and XELIRINOX regimens are feasible and warrant further investigation in combination with targeted therapy in metastatic
 colorectal cancer patients.
 
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-8DOI 10.1007/s00280-011-1764-zAuthors
		T. Mazard, Département d’Oncologie Médicale, CHU Saint Eloi, Montpellier, FranceM. Ychou, Département d’Oncologie Médicale, CHU Saint Eloi, Montpellier, FranceS. Thezenas, Département de Biostatistiques, Centre Val d’Aurelle, Montpellier, FranceS. Poujol, Département de Pharmacie et de Pharmacologie, Centre Val d’Aurelle, Montpellier, FranceF. Pinguet, Département de Pharmacie et de Pharmacologie, Centre Val d’Aurelle, Montpellier, FranceA. Thirion, Département de Recherche Clinique, Cent...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5407132</comments>
            <pubDate>Tue, 08 Nov 2011 19:16:03 +0100</pubDate>
            <guid isPermaLink="false">5407132</guid>        </item>
        <item>
            <title>A phase I pharmacokinetic study of bexarotene with paclitaxel and carboplatin in patients with advanced non-small cell lung cancer (NSCLC)</title>
            <link>http://www.medworm.com/index.php?rid=5384565&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fg1608g246226467q%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;The administration of bexarotene, paclitaxel, and carboplatin is feasible and safe; however, the increased bexarotene plasma
 concentrations and exposure warrant further investigation if this combination is to be utilized clinically.
 
 
 
 
	Content Type Journal ArticleCategory Clinical Trial ReportPages 1-10DOI 10.1007/s00280-011-1770-1Authors
		Jordi Rodon, Institute for Drug Development, Cancer Therapy and Research Center at The University of Texas Health Science Center, San Antonio, TX, USACharlotte D. Jacobs, Division of Oncology, Department of Medicine, Stanford University and Stanford Cancer Institute, 875 Blake Wilbur Drive, Stanford, CA 94305-5826, USAQuincy Chu, Institute for Drug Development, Cancer Therapy and Research Center at The University of Texas H...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5384565</comments>
            <pubDate>Sat, 05 Nov 2011 17:10:18 +0100</pubDate>
            <guid isPermaLink="false">5384565</guid>        </item>
        <item>
            <title>The effect of bexarotene on atorvastatin pharmacokinetics: results from a phase I trial of bexarotene plus chemotherapy in patients with advanced non-small cell lung cancer</title>
            <link>http://www.medworm.com/index.php?rid=5384567&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ff500803l8xu76302%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;A drug–drug interaction was seen in this trial with bexarotene co-administration leading to a significant reduction in the
 AUC of atorvastatin. The likely mechanism for this interaction is through induction of CYP3A4 by bexarotene given the role
 of this enzyme in the metabolism of atorvastatin. Knowledge of this interaction is important for optimizing lipid management
 with atorvastatin for patients receiving bexarotene.
 
 
 
 
	Content Type Journal ArticleCategory Clinical Trial ReportPages 1-9DOI 10.1007/s00280-011-1772-zAuthors
		Heather A. Wakelee, Division of Oncology, Department of Medicine, Stanford University and Stanford Cancer Institute, 875 Blake Wilbur Drive, Stanford, CA 94305-5826, USAChris H. Takimoto, Institute for Drug Development, Cancer Therap...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5384567</comments>
            <pubDate>Sat, 05 Nov 2011 17:10:17 +0100</pubDate>
            <guid isPermaLink="false">5384567</guid>        </item>
        <item>
            <title>A phase I pharmacokinetic study of bexarotene with vinorelbine and cisplatin in patients with advanced non-small-cell lung cancer (NSCLC)</title>
            <link>http://www.medworm.com/index.php?rid=5384566&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fp3712105p7158g83%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;Bexarotene does not substantially affect vinorelbine or cisplatin PK, and the combination is well tolerated. The results are
 consistent with the mechanisms of elimination of vinorelbine (high metabolic clearance) and cisplatin (non-enzymatic and renal
 elimination).
 
 
 
 
	Content Type Journal ArticleCategory Clinical Trial ReportPages 1-10DOI 10.1007/s00280-011-1771-0Authors
		Heather A. Wakelee, Division of Oncology, Department of Medicine, Stanford University and Stanford Cancer Institute, 875 Blake Wilbur Drive, Stanford, CA 94305-5826, USAGary Middleton, St. Luke’s Cancer Centre, Royal Surrey County Hospital, Guildford, UKDavid Dunlop, Beatson West of Scotland Cancer Centre, Glasgow, Scotland, UKRodryg Ramlau, Poznan University of Medical Sciences, Poznan, ...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5384566</comments>
            <pubDate>Sat, 05 Nov 2011 17:10:17 +0100</pubDate>
            <guid isPermaLink="false">5384566</guid>        </item>
        <item>
            <title>The effect of food on the bioavailability of panobinostat, an orally active pan-histone deacetylase inhibitor, in patients with advanced cancer</title>
            <link>http://www.medworm.com/index.php?rid=5384568&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F71l412483126r1m2%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;Food produced minor changes in oral panobinostat exposure; thus, panobinostat can be given without regard to food intake in
 future clinical studies.
 
 
 
 
	Content Type Journal ArticleCategory Clinical Trial ReportPages 1-8DOI 10.1007/s00280-011-1758-xAuthors
		Geoffrey I. Shapiro, Early Drug Development Center, Department of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA, USARichard Frank, Whittingham Cancer Center at Norwalk Hospital, Norwalk, CT, USAUday B. Dandamudi, Section of Clinical Pharmacology, Department of Medicine, Dartmouth-Hitchcock Medical Center and Dartmouth Medical School, Lebanon, NH 03756, USAThomas Hengelage, Novartis Pharma AG, Basel, SwitzerlandLily Zhao, Novartis Oncology, East Hanover, NJ, USALucien Gaz...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5384568</comments>
            <pubDate>Sat, 05 Nov 2011 17:10:16 +0100</pubDate>
            <guid isPermaLink="false">5384568</guid>        </item>
        <item>
            <title>The shape of the myelosuppression time profile is related to the probability of developing neutropenic fever in patients with docetaxel-induced grade IV neutropenia</title>
            <link>http://www.medworm.com/index.php?rid=5384569&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fkl62563518j59554%2F</link>
            <description>Conclusion&amp;nbsp;&amp;nbsp;The probability to develop FN in patients who experience grade IV neutropenia was dependent on the myelosuppression time profile.
 Patients with a rapid neutrophil decline and high drug sensitivity had a higher probability to develop FN. Model-based parameter
 estimates were superior predictors over descriptive values such as the nadir or duration of neutropenia.
 
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-10DOI 10.1007/s00280-011-1769-7Authors
		Emma K. Hansson, Department of Pharmaceutical Biosciences, Uppsala University, Box 591, 751 24 Uppsala, SwedenLena E. Friberg, Department of Pharmaceutical Biosciences, Uppsala University, Box 591, 751 24 Uppsala, Sweden
	

	
		Journal Cancer Chemotherapy and PharmacologyOnline ISSN 1432-0843Print IS...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5384569</comments>
            <pubDate>Fri, 04 Nov 2011 16:56:23 +0100</pubDate>
            <guid isPermaLink="false">5384569</guid>        </item>
        <item>
            <title>A phase I study of vinflunine in combination with capecitabine in patients with metastatic breast cancer previously treated with anthracyclines and taxanes</title>
            <link>http://www.medworm.com/index.php?rid=5384570&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fh7256r4566p11n23%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;The combination of vinflunine and capecitabine is safe and showed promising antitumour activity in MBC patients who have failed
 prior anthracyclines and taxanes. Further clinical development of this combination is warranted.
 
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-9DOI 10.1007/s00280-011-1767-9Authors
		M. Campone, Centre René Gauducheau, Nantes-Saint-Herblain, FranceN. Isambert, Centre Georges-François Leclerc, Dijon, FranceE. Bourbouloux, Centre René Gauducheau, Nantes-Saint-Herblain, FranceH. Roché, Institut Claudius Regaud, Toulouse, FranceJ. Bonneterre, Centre Oscar Lambret, Lille, FranceG. Milano, Centre Antoine Lacassagne, Nice, FranceP. Fumoleau, Centre Georges-François Leclerc, Dijon, France
	

	
		Journal Cancer Chemother...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5384570</comments>
            <pubDate>Tue, 01 Nov 2011 16:51:39 +0100</pubDate>
            <guid isPermaLink="false">5384570</guid>        </item>
        <item>
            <title>Pharmacokinetic and pharmacodynamic study on amrubicin and amrubicinol in Japanese patients with lung cancer</title>
            <link>http://www.medworm.com/index.php?rid=5384572&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F0144l162463l75r4%2F</link>
            <description>Conclusion&amp;nbsp;&amp;nbsp;The pharmacokinetic profiles of amrubicin and amrubicinol were clarified, and the subsequent PK–PD analyses indicate that
 the clearance of amrubicinol is the major determinant of neutropenia.
 
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-9DOI 10.1007/s00280-011-1768-8Authors
		Yoshinori Makino, Department of Pharmacy, National Cancer Center Hospital, 5-1-1 Tsukiji, Chuo-ku, Tokyo, 104-0045 JapanNoboru Yamamoto, Division of Internal Medicine and Thoracic Oncology, National Cancer Center Hospital, 5-1-1 Tsukiji, Chuo-ku, Tokyo, 104-0045 JapanHitoshi Sato, Clinical and Molecular Pharmacokinetics/Pharmacodynamics, School of Pharmaceutical Sciences, Showa University, 1-5-8 Hatanodai, Shinagawa-ku, Tokyo, 142-8555 JapanReiko Ando, Department of Ph...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5384572</comments>
            <pubDate>Mon, 31 Oct 2011 16:50:30 +0100</pubDate>
            <guid isPermaLink="false">5384572</guid>        </item>
        <item>
            <title>A systematic approach to the management of patients with brain metastases of known or unknown primary site</title>
            <link>http://www.medworm.com/index.php?rid=5384571&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F88jk744777011w37%2F</link>
            <description>Conclusion&amp;nbsp;&amp;nbsp;Brain metastases should be treated aggressively and independently of the primary site tumor especially if the performance
 status of the patient is good. The role of chemotherapy should be addressed in the context of clinical trials.
 
 
 
 
	Content Type Journal ArticleCategory Mini ReviewPages 1-13DOI 10.1007/s00280-011-1775-9Authors
		Athanassios P. Kyritsis, Neurosurgical Research Institute, University of Ioannina, 45110 Ioannina, GreeceSofia Markoula, Department of Neurology, School of Medicine, University of Ioannina, University Campus, 45110 Ioannina, GreeceVictor A. Levin, Professor Emeritus, Department of Neuro-Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA
	

	
		Journal Cancer Chemotherapy and PharmacologyOnline ISSN 143...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5384571</comments>
            <pubDate>Mon, 31 Oct 2011 16:50:30 +0100</pubDate>
            <guid isPermaLink="false">5384571</guid>        </item>
        <item>
            <title>Ridaforolimus for patients with progressive or recurrent malignant glioma: a perisurgical, sequential, ascending-dose trial</title>
            <link>http://www.medworm.com/index.php?rid=5384573&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fb646r5460t8l3545%2F</link>
            <description>Conclusion&amp;nbsp;&amp;nbsp;Results suggest that ridaforolimus can cross the blood–brain barrier in areas of tumor involvement, and may inhibit mTOR activity
 in advanced gliomas based on decreased pS6 levels. This perisurgical trial design should serve as a template for evaluating
 intratumoral pharmacokinetics and pharmacodynamics of other targeted agents in this patient population.
 
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-12DOI 10.1007/s00280-011-1773-yAuthors
		David A. Reardon, Center for Neuro-Oncology, Dana-Farber Cancer Institute, 450 Brookline Avenue—SW G460F, Boston, MA 02215, USAPatrick Y. Wen, Center for Neuro-Oncology, Dana-Farber/Brigham and Women’s Cancer Center, 44 Binney Street, Shields Warren 430 D, Boston, MA 02115, USAW. K. Alfred Yung, Depa...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5384573</comments>
            <pubDate>Sun, 30 Oct 2011 05:37:54 +0100</pubDate>
            <guid isPermaLink="false">5384573</guid>        </item>
        <item>
            <title>ABT-263 sensitizes TRAIL-resistant hepatocarcinoma cells by downregulating the Bcl-2 family of anti-apoptotic protein</title>
            <link>http://www.medworm.com/index.php?rid=5384574&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F9348237251k2w135%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;These findings provide a novel insight into the clinical application of TRAIL-induced apoptosis of HCC cells.
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-7DOI 10.1007/s00280-011-1763-0Authors
		Guan Wang, College of Life Sciences, Wuhan University, Wuhan, 430072 ChinaYao Zhan, College of Life Sciences, Wuhan University, Wuhan, 430072 ChinaHaiqing Wang, College of Life Sciences, Wuhan University, Wuhan, 430072 ChinaWenhua Li, College of Life Sciences, Wuhan University, Wuhan, 430072 China
	

	
		Journal Cancer Chemotherapy and PharmacologyOnline ISSN 1432-0843Print ISSN 0344-5704 (Source: Cancer Chemotherapy and Pharmacology)</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5384574</comments>
            <pubDate>Sat, 29 Oct 2011 05:50:22 +0100</pubDate>
            <guid isPermaLink="false">5384574</guid>        </item>
        <item>
            <title>Intrapleural paclitaxel for malignant pleural effusion from ovarian and breast cancer: a phase II study with pharmacokinetic analysis</title>
            <link>http://www.medworm.com/index.php?rid=5384575&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fg2t74n9v521705nl%2F</link>
            <description>Conclusion&amp;nbsp;&amp;nbsp;Intrapleural paclitaxel is a safe and effective palliative treatment for MPE from breast and ovarian cancers and may be integrated
 with systemic chemotherapy.
 
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-7DOI 10.1007/s00280-011-1765-yAuthors
		Giuseppe Lombardi, Medical Oncology 1, Istituto Oncologico Veneto—IRCCS, Padova, ItalyMaria Ornella Nicoletto, Medical Oncology 1, Istituto Oncologico Veneto—IRCCS, Padova, ItalyMilena Gusella, Department of Oncology, ULSS 18, Rovigo, ItalyPasquale Fiduccia, Medical Oncology 1, Istituto Oncologico Veneto—IRCCS, Padova, ItalyMaurizia Dalla Palma, Medical Oncology 1, Istituto Oncologico Veneto—IRCCS, Padova, ItalyAndrea Zuin, Division of Thoracic Surgery, Department of Cardio-Thoracic and Vascular...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5384575</comments>
            <pubDate>Sat, 29 Oct 2011 05:50:21 +0100</pubDate>
            <guid isPermaLink="false">5384575</guid>        </item>
        <item>
            <title>Pharmacokinetics, metabolism and excretion of [14C]-lenalidomide following oral administration in healthy male subjects</title>
            <link>http://www.medworm.com/index.php?rid=5384576&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fy1345551563u1742%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;In summary, following oral administration, lenalidomide is highly absorbed and bioavailable, metabolized minimally, and eliminated
 predominantly via urinary excretion in the unchanged form in humans.
 
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-9DOI 10.1007/s00280-011-1760-3Authors
		Nianhang Chen, Clinical Pharmacology, Celgene Corporation, 86 Morris Avenue, Summit, NJ 07920, USALian Wen, ABC Laboratories, Columbia, MO, USAHenry Lau, Clinical Pharmacology, Celgene Corporation, 86 Morris Avenue, Summit, NJ 07920, USASekhar Surapaneni, Nonclinical Development, Celgene Corporation, 86 Morris Avenue, Summit, NJ 07920, USAGondi Kumar, Nonclinical Development, Celgene Corporation, 86 Morris Avenue, Summit, NJ 07920, USA
	

	
		Journal Cancer Chem...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5384576</comments>
            <pubDate>Sat, 29 Oct 2011 05:50:20 +0100</pubDate>
            <guid isPermaLink="false">5384576</guid>        </item>
        <item>
            <title>Phase II trial of sorafenib in combination with 5-fluorouracil infusion in advanced hepatocellular carcinoma</title>
            <link>http://www.medworm.com/index.php?rid=5359963&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fw68658053766706r%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;The results show an encouraging disease control rate, time to progression, and overall survival. The combination of sorafenib
 and 5-fluorouracil was feasible, and the side effects were manageable for patients carefully selected for liver function and
 performance status.
 
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-8DOI 10.1007/s00280-011-1753-2Authors
		Iacopo Petrini, Department of Oncology, Transplant and New Advances in Medicine, BIOS, University of Pisa, 67 Via Roma, 56126 Pisa, ItalyMonica Lencioni, Medical Oncology, Pisa University Hospital, Pisa, ItalyMiriam Ricasoli, Medical Oncology, Pisa University Hospital, Pisa, ItalyMauro Iannopollo, Medical Oncology, Pisa University Hospital, Pisa, ItalyCinzia Orlandini, Medical Oncology, Pisa...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5359963</comments>
            <pubDate>Fri, 28 Oct 2011 06:06:00 +0100</pubDate>
            <guid isPermaLink="false">5359963</guid>        </item>
        <item>
            <title>First-time-in-human study of GSK923295, a novel antimitotic inhibitor of centromere-associated protein E (CENP-E), in patients with refractory cancer</title>
            <link>http://www.medworm.com/index.php?rid=5346891&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fp65v8144t3052n21%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;The novel CENP-E inhibitor, GSK923295, had dose-proportional pharmacokinetics and a low number of grade 3 or 4 adverse events.
 The observed incidence of myelosuppression and neuropathy was low. Further investigations may provide a more complete understanding
 of the potential for GSK923295 as an antiproliferative agent.
 
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-9DOI 10.1007/s00280-011-1756-zAuthors
		Vincent Chung, City of Hope Medical Center, 1500 East Duarte Road, Durate, CA 91010, USAElisabeth I. Heath, Karmanos Cancer Center, Detroit, MI, USAWilliam R. Schelman, University of Wisconsin Carbone Cancer Center, Madison, WI, USABrendan M. Johnson, GlaxoSmithKline, Research Triangle Park, NC, USALyndon C. Kirby, GlaxoSmithKline, Research T...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5346891</comments>
            <pubDate>Fri, 21 Oct 2011 15:59:43 +0100</pubDate>
            <guid isPermaLink="false">5346891</guid>        </item>
        <item>
            <title>A randomized phase II study of two doses of vorinostat in combination with 5-FU/LV in patients with refractory colorectal cancer</title>
            <link>http://www.medworm.com/index.php?rid=5346890&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fp743t57561881334%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;While the addition of vorinostat to 5-FU resulted in 1 partial response and in some disease stabilizations, the limited activity
 does not warrant the unselected use of this combination in chemotherapy-refractory colorectal cancer.
 
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-9DOI 10.1007/s00280-011-1762-1Authors
		M. G. Fakih, Department of Medicine, University of Michigan, Ann Arbor, MI, USAA. Groman, Department of Biostatistics, University at Buffalo, Buffalo, NY, USAJ. McMahon, Clinical Research Services, Roswell Park Cancer Institute, Buffalo, NY, USAG. Wilding, Department of Biostatistics, University at Buffalo, Buffalo, NY, USAJ. R. Muindi, Department of Medicine, Roswell Park Cancer Institute, Buffalo, NY, USA
	

	
		Journal Cancer Ch...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5346890</comments>
            <pubDate>Fri, 21 Oct 2011 15:59:43 +0100</pubDate>
            <guid isPermaLink="false">5346890</guid>        </item>
        <item>
            <title>Phase I rapid dose-escalation study of AGS-1C4D4, a human anti-PSCA (prostate stem cell antigen) monoclonal antibody, in patients with castration-resistant prostate cancer: a PCCTC trial</title>
            <link>http://www.medworm.com/index.php?rid=5346889&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F8h043v00v1p78332%2F</link>
            <description>Conclusion&amp;nbsp;&amp;nbsp;AGS-1C4D4 was well-tolerated and demonstrated linear PK. Despite preclinical differences in antibody-dependent cellular cytotoxicity,
 AGS-1C4D4 and AGS-PSCA have similar safety and PK profiles. The recommended Phase II dose is 48&amp;nbsp;mg/kg.
 
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-9DOI 10.1007/s00280-011-1759-9Authors
		Emmanuel S. Antonarakis, Prostate Cancer Research Program, Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins, Johns Hopkins University School of Medicine, CRB1-1M59, 1650 Orleans Street, Baltimore, MD 21231, USAMichael A. Carducci, Prostate Cancer Research Program, Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins, Johns Hopkins University School of Medicine, CRB1-1M59, 1650 Orleans Street, Baltimore, MD...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5346889</comments>
            <pubDate>Fri, 21 Oct 2011 15:59:43 +0100</pubDate>
            <guid isPermaLink="false">5346889</guid>        </item>
        <item>
            <title>Effect of food and a proton pump inhibitor on the pharmacokinetics of S-1 following oral administration of S-1 in patients with advanced solid tumors</title>
            <link>http://www.medworm.com/index.php?rid=5346892&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fn02w30522g158862%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;Oxo exposure was reduced under fed compared to fasting condition. To increase the bioavailability of S-1, the administration
 of S-1 under fasting condition was more effective in the western countries.
 
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-9DOI 10.1007/s00280-011-1761-2Authors
		Max E. Scheulen, West German Cancer Center, University of Essen, Essen, GermanyKaku Saito, Taiho Pharma USA, Inc, 202 Carnegie Center, Suite 100, Princeton, NJ 08550, USARalf A. Hilger, West German Cancer Center, University of Essen, Essen, GermanyBastian Mende, West German Cancer Center, University of Essen, Essen, GermanyChristopher Zergebel, Taiho Pharma USA, Inc, 202 Carnegie Center, Suite 100, Princeton, NJ 08550, USADirk Strumberg, University of Bochum (M...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5346892</comments>
            <pubDate>Fri, 21 Oct 2011 15:59:40 +0100</pubDate>
            <guid isPermaLink="false">5346892</guid>        </item>
        <item>
            <title>Safety and pharmacokinetics of high-dose gefitinib in patients with solid tumors: results of a phase I study</title>
            <link>http://www.medworm.com/index.php?rid=5323661&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fe723176080481484%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;Exposure to gefitinib did not increase consistently with increasing dose beyond gefitinib 1,500&amp;nbsp;mg once-weekly or twice-weekly.
 These data do not support further evaluation of gefitinib at high-dose schedules.
 
 
 
 
	Content Type Journal ArticleCategory Clinical Trial ReportPages 1-8DOI 10.1007/s00280-011-1757-yAuthors
		Mitchell E. Gross, Center for Applied Molecular Medicine, University of Southern California Westside Cancer Center, Beverly Hills, CA, USALawrence Leichman, Comprehensive Cancer Center and Desert Regional Medical Center, Palm Springs, CA, USAElizabeth S. Lowe, AstraZeneca, Wilmington, DE, USAAlan Swaisland, AstraZeneca, Macclesfield, Cheshire, UKDavid B. Agus, Center for Applied Molecular Medicine, University of Southern California Westside C...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5323661</comments>
            <pubDate>Sat, 15 Oct 2011 05:53:14 +0100</pubDate>
            <guid isPermaLink="false">5323661</guid>        </item>
        <item>
            <title>miR-200bc/429 cluster modulates multidrug resistance of human cancer cell lines by targeting BCL2 and XIAP</title>
            <link>http://www.medworm.com/index.php?rid=5323662&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F5353688831pt8365%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;Our findings first suggest that miR-200bc/429 cluster could play a role in the development of MDR in both gastric and lung
 cancer cell lines, at least in part by modulation of apoptosis via targeting BCL2 and XIAP.
 
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-9DOI 10.1007/s00280-011-1752-3Authors
		Wei Zhu, Department of Oncology, First Affiliated Hospital of Nanjing Medical University, 300 Guangzhou Road, Nanjing, 210029 ChinaHuaguo Xu, Department of Clinical Laboratory, First Affiliated Hospital of Nanjing Medical University, 300 Guangzhou Road, Nanjing, 210029 ChinaDanXia Zhu, Department of Haematology, First Affiliated Hospital of Nanjing Medical University, 300 Guangzhou Road, Nanjing, 210029 ChinaHui Zhi, Department of Oncology, First ...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5323662</comments>
            <pubDate>Thu, 13 Oct 2011 05:48:37 +0100</pubDate>
            <guid isPermaLink="false">5323662</guid>        </item>
        <item>
            <title>A phase I dose-escalation and pharmacokinetic study of sunitinib in combination with pemetrexed in patients with advanced solid malignancies, with an expanded cohort in non-small cell lung cancer</title>
            <link>http://www.medworm.com/index.php?rid=5313882&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F87674k44x8505213%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;In patients with advanced solid malignancies, the MTD of sunitinib plus 500&amp;nbsp;mg/m2 pemetrexed was 37.5&amp;nbsp;mg/day (CDD schedule) or 50&amp;nbsp;mg/day (Schedule 2/1). The CDD schedule MTD was tolerable and demonstrated
 promising clinical benefit in NSCLC.
 
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-14DOI 10.1007/s00280-011-1755-0Authors
		L. Q. M. Chow, The Ottawa Hospital Cancer Centre, Ottawa, CanadaN. Blais, Centre de Lutte Contre le Cancer du CHUM, Montreal, CanadaD. J. Jonker, The Ottawa Hospital Cancer Centre, Ottawa, CanadaS. A. Laurie, The Ottawa Hospital Cancer Centre, Ottawa, CanadaS. G. Diab, Colorado Integrative Cancer Care, Aurora, CO, USAC. Canil, The Ottawa Hospital Cancer Centre, Ottawa, CanadaM. McWilliam, The Ottawa Hospi...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5313882</comments>
            <pubDate>Wed, 12 Oct 2011 05:42:48 +0100</pubDate>
            <guid isPermaLink="false">5313882</guid>        </item>
        <item>
            <title>In vitro evaluation of clinical activity and toxicity of anticancer drugs using tumor cells from patients and cells representing normal tissues</title>
            <link>http://www.medworm.com/index.php?rid=5313883&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F9530ml9j12l87401%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;In preclinical drug development, primary tumor cells from patients can be used for the prediction of cancer diagnosis–specific
 activity and may aid in the selection of diagnoses for clinical trials. By using tumor and toxicity panels together, information
 about therapeutic index may be derived, which may be useful when choosing among drug candidates with similar tumor effects.
 
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-11DOI 10.1007/s00280-011-1746-1Authors
		Caroline Haglund, Division of Clinical Pharmacology, Department of Medical Sciences, Uppsala University, Uppsala, SwedenAnna Åleskog, Division of Haematology, Department of Medical Sciences, Uppsala University, Uppsala, SwedenPeter Nygren, Division of Clinical Pharmacology, Depart...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5313883</comments>
            <pubDate>Sun, 09 Oct 2011 05:36:30 +0100</pubDate>
            <guid isPermaLink="false">5313883</guid>        </item>
        <item>
            <title>Pharmacokinetic drug interaction between AEE788 and RAD001 causing thrombocytopenia in patients with glioblastoma</title>
            <link>http://www.medworm.com/index.php?rid=5313884&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fn4q85q03154x145q%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;The coadministration of AEE788 and RAD001 in glioblastoma patients caused a clinically significant thrombocytopenia and a
 higher-than-expected RAD001 area under the curve concentration when dosed at 200 and 5&amp;nbsp;mg/day, respectively. After a dose
 reduction to AEE788 (150&amp;nbsp;mg/day) and RAD001 (5&amp;nbsp;mg qod), the combination appeared to be better tolerated.
 
 
 
 
	Content Type Journal ArticleCategory Short CommunicationPages 1-7DOI 10.1007/s00280-011-1754-1Authors
		David A. Reardon, Center for Neuro-Oncology, Dana-Farber Cancer Institute, 450 Brookline Avenue, SW-460F, Boston, MA 02215, USATimothy Cloughesy, University of California, Los Angeles, Los Angeles, CA, USAJeremy Rich, Cleveland Clinic Lerner Research Institute, Cleveland, OH, USAW. K. Alfred Yung,...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5313884</comments>
            <pubDate>Sat, 08 Oct 2011 15:45:02 +0100</pubDate>
            <guid isPermaLink="false">5313884</guid>        </item>
        <item>
            <title>The role of MTHFR and RFC1 polymorphisms on toxicity and outcome of adult patients with hematological malignancies treated with high-dose methotrexate followed by leucovorin rescue</title>
            <link>http://www.medworm.com/index.php?rid=5313885&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fm7rq8576n600v345%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;Leucovorin rescue given after high-dose MTX probably accounts for the lack of influence of C677T polymorphism. To better define
 a role of RFC1 polymorphism on patients outcome, it would be worthwhile to perform a study on intracellular MTX level and
 RFC1 substrate binding affinities in different genotypes.
 
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-6DOI 10.1007/s00280-011-1751-4Authors
		Patrizia Chiusolo, Department of Hematology, Università Cattolica del Sacro Cuore, Largo A. Gemelli 8, 00168 Rome, ItalySabrina Giammarco, Department of Hematology, Università Cattolica del Sacro Cuore, Largo A. Gemelli 8, 00168 Rome, ItalySilvia Bellesi, Department of Hematology, Università Cattolica del Sacro Cuore, Largo A. Gemelli 8, 00168 Rome, It...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5313885</comments>
            <pubDate>Sat, 08 Oct 2011 15:45:01 +0100</pubDate>
            <guid isPermaLink="false">5313885</guid>        </item>
        <item>
            <title>Impact of plasma and intracellular exposure and CYP3A4, CYP3A5, and ABCB1 genetic polymorphisms on vincristine-induced neurotoxicity</title>
            <link>http://www.medworm.com/index.php?rid=5296604&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F9785746n33216422%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;None of the different genetic covariates nor plasma and intracellular exposure was predictive of the observed neurotoxicity
 in our pediatric population. Nevertheless, the heterozygote diplotype of ABCB1 appears to influence the intracellular accumulation of vincristine. Owing to the small sample size, further evaluations are
 needed in a larger patient cohort.
 
 
 
 
	Content Type Journal ArticleCategory Short CommunicationPages 1-6DOI 10.1007/s00280-011-1745-2Authors
		Romain Guilhaumou, Aix-Marseille Univ, CRO2, INSERM, UMR 911, 13385 Marseille, FranceCaroline Solas, Aix-Marseille Univ, CRO2, INSERM, UMR 911, 13385 Marseille, FranceVeronique Bourgarel-Rey, Aix-Marseille Univ, CRO2, INSERM, UMR 911, 13385 Marseille, FranceSylvie Quaranta, Laboratoire de Pharmacoci...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5296604</comments>
            <pubDate>Tue, 04 Oct 2011 05:50:36 +0100</pubDate>
            <guid isPermaLink="false">5296604</guid>        </item>
        <item>
            <title>Enhancement of curcumin oral absorption and pharmacokinetics of curcuminoids and curcumin metabolites in mice</title>
            <link>http://www.medworm.com/index.php?rid=5296605&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fglv88170035vg131%2F</link>
            <description>Conclusion&amp;nbsp;&amp;nbsp;This oral absorption enhanced NEC may provide a practical formulation to conduct the correlative study of the PK of curcuminoids
 and their pharmacodynamics, e.g., hypomethylation activity in vivo.
 
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-11DOI 10.1007/s00280-011-1749-yAuthors
		Liu Zhongfa, College of Pharmacy, The Ohio State University, Room 152, Riffe Building, 500 W. 12th Avenue, Columbus, OH 43210, USAMing Chiu, College of Pharmacy, The Ohio State University, Room 152, Riffe Building, 500 W. 12th Avenue, Columbus, OH 43210, USAJiang Wang, College of Pharmacy, The Ohio State University, Room 152, Riffe Building, 500 W. 12th Avenue, Columbus, OH 43210, USAWei Chen, College of Pharmacy, The Ohio State University, Room 152, Riffe Building...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5296605</comments>
            <pubDate>Tue, 04 Oct 2011 05:50:34 +0100</pubDate>
            <guid isPermaLink="false">5296605</guid>        </item>
        <item>
            <title>Phase II study of use of a single cycle of induction chemotherapy and concurrent chemoradiotherapy containing capecitabine/cisplatin followed by surgery for patients with resectable esophageal squamous cell carcinoma: long-term follow-up data</title>
            <link>http://www.medworm.com/index.php?rid=5296606&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F8774198224710517%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;A trimodal approach, consisting of a single cycle of induction chemotherapy, CRT containing capecitabine and cisplatin, and
 surgery, was feasible and effective in patients with resectable esophageal squamous cell carcinoma.
 
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-9DOI 10.1007/s00280-011-1750-5Authors
		Dong Hoe Koo, Department of Oncology, University of Ulsan College of Medicine, Esophageal Cancer Study Group (ECSG), Asan Medical Center, 86, Asanbyeongwon-gil, Songpa-gu, Seoul, 138-736 KoreaSeung-Il Park, Department of Thoracic Surgery, University of Ulsan College of Medicine, Esophageal Cancer Study Group (ECSG), Asan Medical Center, Seoul, KoreaYong-Hee Kim, Department of Thoracic Surgery, University of Ulsan College of Medicine, Esop...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5296606</comments>
            <pubDate>Tue, 04 Oct 2011 05:50:33 +0100</pubDate>
            <guid isPermaLink="false">5296606</guid>        </item>
        <item>
            <title>Debio 0507 primarily forms diaminocyclohexane-Pt-d(GpG) and -d(ApG) DNA adducts in HCT116 cells</title>
            <link>http://www.medworm.com/index.php?rid=5296607&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fyt4610q73t258026%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;These data show that the major DNA adducts formed by Debio 0507 are the dach-Pt-d(GpG) and dach-Pt-d(ApG) adducts and at equitoxic
 doses Debio 0507 and oxaliplatin form similar levels of dach-Pt-d(GpG) and dach-Pt-d(ApG) adducts. This suggests that the
 action mechanisms of Debio 0507 and oxaliplatin are similar at a cellular level.
 
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-13DOI 10.1007/s00280-011-1744-3Authors
		C. L. King, Department of Biochemistry and Biophysics, School of Medicine, University of North Carolina, CB #7260, Genetic Medicine Building, Chapel Hill, NC 27599-7260, USAS. Ramachandran, Department of Biochemistry and Biophysics, School of Medicine, University of North Carolina, CB #7260, Genetic Medicine Building, Chapel Hil...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5296607</comments>
            <pubDate>Tue, 04 Oct 2011 05:50:32 +0100</pubDate>
            <guid isPermaLink="false">5296607</guid>        </item>
        <item>
            <title>Pharmacokinetics of TH-302: a hypoxically activated prodrug of bromo-isophosphoramide mustard in mice, rats, dogs and monkeys</title>
            <link>http://www.medworm.com/index.php?rid=5285169&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fw374r60950237mh1%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;TH-302 exhibited good safety, efficacy and pharmacokinetic properties in nonclinical species, translating into favorable properties
 in humans.
 
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-12DOI 10.1007/s00280-011-1741-6Authors
		Donald Jung, Department of Nonclinical and Clinical Pharmacology, Threshold Pharmaceuticals, Inc., 170 Harbor Way, Suite 300, South San Francisco, CA 94080, USALin Lin, Department of Nonclinical and Clinical Pharmacology, Threshold Pharmaceuticals, Inc., 170 Harbor Way, Suite 300, South San Francisco, CA 94080, USAHailong Jiao, Department of Medicinal Chemistry, Threshold Pharmaceuticals, Inc., South San Francisco, CA, USAXiaohong Cai, Department of Medicinal Chemistry, Threshold Pharmaceuticals, Inc., South San Fran...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5285169</comments>
            <pubDate>Sat, 01 Oct 2011 06:45:04 +0100</pubDate>
            <guid isPermaLink="false">5285169</guid>        </item>
        <item>
            <title>Phase II study of weekly docetaxel and fixed dose rate gemcitabine in patients with previously treated advanced soft tissue and bone sarcoma</title>
            <link>http://www.medworm.com/index.php?rid=5285170&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fk006461131087752%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;The combination of weekly docetaxel and fixed dose rate gemcitabine was tolerable and may be an active regimen in patients
 with previously treated advanced sarcoma.
 
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-8DOI 10.1007/s00280-011-1742-5Authors
		Eun Mi Lee, Department of Oncology, Asan Medical Center, University of Ulsan College of Medicine, 388-1 Pungnap-Dong Songpa-Gu, Seoul, 138-736 KoreaSun Young Rha, Division of Medical Oncology, Department of Internal Medicine, Yonsei Cancer Center, Yonsei University College of Medicine, Seoul, KoreaJeeyun Lee, Division of Hematology and Oncology, Department of Internal Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, KoreaKyong Hwa Park, Division of Hematology a...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5285170</comments>
            <pubDate>Fri, 30 Sep 2011 05:53:14 +0100</pubDate>
            <guid isPermaLink="false">5285170</guid>        </item>
        <item>
            <title>A phase I, open-label, randomized crossover study to assess the effect of dosing of the MEK 1/2 inhibitor Selumetinib (AZD6244; ARRY-142866) in the presence and absence of food in patients with advanced solid tumors</title>
            <link>http://www.medworm.com/index.php?rid=5273234&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fy88g472558848451%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;The presence of food decreased the extent of absorption of selumetinib. It is recommended that for further clinical studies,
 selumetinib be taken on an empty stomach. Selumetinib demonstrated an acceptable safety profile in the advanced cancer population.
 
 
 
 
	Content Type Journal ArticleCategory Clinical Trial ReportPages 1-10DOI 10.1007/s00280-011-1732-7Authors
		Suzanne Leijen, Division of Experimental Therapy, The Netherlands Cancer Institute, Plesmanlaan 121, 1066 CX Amsterdam, The NetherlandsPatricia M. M. B. Soetekouw, Division of Medical Oncology, Department of Internal Medicine, GROW—School for Oncology and Developmental Biology, Maastricht University Medical Centre, Maastricht, The NetherlandsT. R. Jeffry Evans, Translational Cancer Research, Beatson...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5273234</comments>
            <pubDate>Wed, 28 Sep 2011 05:51:06 +0100</pubDate>
            <guid isPermaLink="false">5273234</guid>        </item>
        <item>
            <title>Targeting autophagy enhances BO-1051-induced apoptosis in human malignant glioma cells</title>
            <link>http://www.medworm.com/index.php?rid=5273235&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fw315056178036262%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;BO-1051 induced both apoptosis and autophagy, and inhibition of autophagy significantly augmented the cytotoxic effect of
 BO-1051. Thus, a combination of BO-1051 and autophagic inhibitors offers a potentially new therapeutic modality for the treatment
 of malignant glioma.
 
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-13DOI 10.1007/s00280-011-1747-0Authors
		Pei-Ming Chu, Graduate Institutes of Life Sciences, National Defense Medical Center, Taipei, Taiwan, ROCLi-Hsin Chen, Institute of Pharmacology, National Yang-Ming University, Taipei, TaiwanMing-Teh Chen, Department of Neurosurgery, Neurological Institute, Taipei Veterans General Hospital, Taipei, TaiwanHsin-I Ma, Graduate Institutes of Life Sciences, National Defense Medical Center, Taip...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5273235</comments>
            <pubDate>Tue, 27 Sep 2011 05:46:35 +0100</pubDate>
            <guid isPermaLink="false">5273235</guid>        </item>
        <item>
            <title>Adjuvant therapy for resectable high-risk soft tissue sarcoma: feasibility and efficacy of a sandwich chemoradiotherapy strategy</title>
            <link>http://www.medworm.com/index.php?rid=5260148&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F2t658581628710u4%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;The sandwich chemoradiation protocol proved to be feasible with manageable toxicity. The patient outcome compared favorably
 with other adjuvant trials in preventing relapse, particularly distant relapse which is predictive of poor outcome. This multidisciplinary
 approach warrants further investigation in a larger randomized trial.
 
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-8DOI 10.1007/s00280-011-1731-8Authors
		Christian H. Brandts, Department of Medicine, Hematology and Oncology, University Hospital Muenster, Albert-Schweitzer-Str. 33, 48149 Muenster, GermanyChristiane Schulz, Department of Medicine, Hematology and Oncology, University Hospital Muenster, Albert-Schweitzer-Str. 33, 48149 Muenster, GermanyNormann Willich, Department of Ra...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5260148</comments>
            <pubDate>Sat, 24 Sep 2011 05:42:46 +0100</pubDate>
            <guid isPermaLink="false">5260148</guid>        </item>
        <item>
            <title>Translational research of a novel humanized epidermal growth factor receptor-related protein: a putative inhibitor of pan-ErbB</title>
            <link>http://www.medworm.com/index.php?rid=5260149&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fb72747770jp70659%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;As rat ERRP protein is expected to generate an immune response in humans, we propose a hypothesis that a humanized version
 of ERRP has potential therapeutic value for cancer patients.
 
 
 
 
	Content Type Journal ArticleCategory Mini ReviewPages 1-4DOI 10.1007/s00280-011-1748-zAuthors
		Xian-Hua Fu, Cancer Institute (Key Laboratory of Cancer Prevention and Intervention, China National Ministry of Education), The Second Affiliated Hospital, School of Medicine, Zhejiang University, 88 Jiefang Road, Hangzhou, Zhejiang Province 310009, People’s Republic of ChinaJun Li, Cancer Institute (Key Laboratory of Cancer Prevention and Intervention, China National Ministry of Education), The Second Affiliated Hospital, School of Medicine, Zhejiang University, 88 Jiefang Road, ...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5260149</comments>
            <pubDate>Fri, 23 Sep 2011 05:54:32 +0100</pubDate>
            <guid isPermaLink="false">5260149</guid>        </item>
        <item>
            <title>An open-label study to describe pharmacokinetic parameters of erlotinib in patients with advanced solid tumors with adequate and moderately impaired hepatic function</title>
            <link>http://www.medworm.com/index.php?rid=5260150&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F10430242xgn27772%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;The PK and safety profiles of erlotinib in patients with MHI were similar to those with AHF. As a result, a reduced starting
 dose of erlotinib in patients with MHI is not required and treatment should be guided by patients’ tolerability.
 
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-8DOI 10.1007/s00280-011-1733-6Authors
		Cindy L. O’Bryant, Department of Clinical Pharmacy, School of Pharmacy, University of Colorado Cancer Center, Mail Stop C238, 12850 East Montview Blvd., V20-1223, Aurora, CO 80045, USAPaul Haluska, Mayo Clinic, Rochester, MN, USALee Rosen, Premiere Oncology, Santa Monica, CA, USARamesh K. Ramanathan, University of Pittsburgh Cancer Institute, Pittsburgh, PA, USABalaji Venugopal, Beatson Oncology Centre, University of Gla...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5260150</comments>
            <pubDate>Thu, 22 Sep 2011 06:38:13 +0100</pubDate>
            <guid isPermaLink="false">5260150</guid>        </item>
        <item>
            <title>Evaluation of a formula for individual dosage of nedaplatin based on renal function</title>
            <link>http://www.medworm.com/index.php?rid=5236797&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F16wnq3l027774t82%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;Ishibashi’s formula would be predictable and useful for estimating the individual dose of NDP.
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-5DOI 10.1007/s00280-011-1739-0Authors
		Shinya Sato, Department of Obstetrics and Gynecology, Tottori University, 36-1, Nishi-cho, Yonago City, Tottori 683 8504, JapanHiroyuki Fujiwara, Department of Obstetrics and Gynecology, Jichi Medical College, Kawachi-gun, Tochigi, JapanTetsuro Oishi, Department of Obstetrics and Gynecology, Tottori University, 36-1, Nishi-cho, Yonago City, Tottori 683 8504, JapanMuneaki Shimada, Department of Obstetrics and Gynecology, Tottori University, 36-1, Nishi-cho, Yonago City, Tottori 683 8504, JapanShizuo Machida, Department of Obstetrics and Gynecology, Jichi Medical Coll...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5236797</comments>
            <pubDate>Thu, 15 Sep 2011 05:53:56 +0100</pubDate>
            <guid isPermaLink="false">5236797</guid>        </item>
        <item>
            <title>A phase I study of daily everolimus plus low-dose weekly cisplatin for patients with advanced solid tumors</title>
            <link>http://www.medworm.com/index.php?rid=5224741&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F247707h460166673%2F</link>
            <description>Conclusion&amp;nbsp;&amp;nbsp;The phase II recommended dose is everolimus 10&amp;nbsp;mg/day (days 1–21)&amp;nbsp;+&amp;nbsp;cisplatin 20&amp;nbsp;mg/m2 (days 1, 8, and 15) of a 28-day cycle. PK data demonstrate dose-proportional increases in exposure, as previously described
 for everolimus monotherapy. Anti-tumor activity was observed in several tumor types.
 
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-8DOI 10.1007/s00280-011-1734-5Authors
		Matthew G. Fury, Department of Medicine, Head and Neck Medical Oncology Service, Memorial Sloan-Kettering Cancer Center, 1275 York Avenue, Box 532, New York, NY 10021, USAEric Sherman, Department of Medicine, Head and Neck Medical Oncology Service, Memorial Sloan-Kettering Cancer Center, 1275 York Avenue, Box 532, New York, NY 10021, USASofia Haqu...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5224741</comments>
            <pubDate>Tue, 13 Sep 2011 05:56:36 +0100</pubDate>
            <guid isPermaLink="false">5224741</guid>        </item>
        <item>
            <title>Drug-induced interstitial lung disease in tyrosine kinase inhibitor therapy for non-small cell lung cancer: a review on current insight</title>
            <link>http://www.medworm.com/index.php?rid=5224742&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fh56582168n746206%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;It is important to recognize the various patterns of TKI-induced ILDs, which increase in incidence with the introduction of
 diverse types of molecularly targeted agents. Poor prognoses are expected when there is a short interval from the initiation
 of target therapy to the onset of ILD, acute interstitial pneumonia pattern of ILD, and preexisting pulmonary fibrosis.
 
 
 
 
	Content Type Journal ArticleCategory Mini ReviewPages 1-11DOI 10.1007/s00280-011-1737-2Authors
		Ji Hye Min, Deparment of Radiology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South KoreaHo Yun Lee, Deparment of Radiology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South KoreaHoyeong Lim, The Division of Hematology-Oncology, Depart...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5224742</comments>
            <pubDate>Tue, 13 Sep 2011 05:56:35 +0100</pubDate>
            <guid isPermaLink="false">5224742</guid>        </item>
        <item>
            <title>Pharmacodynamics of DT-IgG, a dual-targeting antibody against VEGF-EGFR, in tumor xenografted mice</title>
            <link>http://www.medworm.com/index.php?rid=5224743&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F82961451u451m850%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;A lower IC50 of DT-IgG partially compensated for lower serum concentrations than bevacizumab and cetuximab, but may require higher doses
 for comparable efficacy as the combination. The model adequately predicted variations of tumor response at the DT-IgG doses
 tested and could be used for targeting specific tumor efficacies for future testing.
 
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-14DOI 10.1007/s00280-011-1713-xAuthors
		Selwyn J. Hurwitz, Center for AIDS Research, Laboratory of Biochemical Pharmacology, Department of Pediatrics, Emory University School of Medicine/VA Medical Center, Medical Research # 151H, 1670 Clairmont Road, Decatur, GA 30300, USAHongzheng Zhang, Department of Hematology and Medical Oncology, Winship Cancer Insti...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5224743</comments>
            <pubDate>Tue, 13 Sep 2011 05:56:33 +0100</pubDate>
            <guid isPermaLink="false">5224743</guid>        </item>
        <item>
            <title>A pilot pharmacologic biomarker study of busulfan and fludarabine in hematopoietic cell transplant recipients</title>
            <link>http://www.medworm.com/index.php?rid=5224744&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fu56712h588u75071%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;The low rates of GvHD, particularly in its chronic form, were encouraging, and further biomarker studies are warranted to
 optimize the fludarabine/Tbusulfan/rATG conditioning regimen.
 
 
 
 
	Content Type Journal ArticleCategory Clinical Trial ReportPages 1-10DOI 10.1007/s00280-011-1736-3Authors
		Jeannine S. McCune, School of Pharmacy, University of Washington, Box 357630, Seattle, WA 98195-7630, USAErica L. Woodahl, School of Pharmacy, University of Washington, Box 357630, Seattle, WA 98195-7630, USATerry Furlong, Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA, USABarry Storer, Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA, USAJoanne Wang, School of Pharmacy, University of Washington, Box 357630, ...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5224744</comments>
            <pubDate>Sat, 10 Sep 2011 15:48:27 +0100</pubDate>
            <guid isPermaLink="false">5224744</guid>        </item>
        <item>
            <title>A phase I-II study of elacytarabine (CP-4055) in the treatment of patients with ovarian cancer resistant or refractory to platinum therapy</title>
            <link>http://www.medworm.com/index.php?rid=5207903&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fw311q10784x13268%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;The RD for elacytarabine was 100&amp;nbsp;mg/m2/day, D1-5 and D8-12 q4w. The safety profile was comparable to the safety profiles reported in previous clinical studies with
 elacytarabine in solid tumours. Despite some longer-lasting disease stabilisations, two of them exceeding the previous progression-free
 interval, further investigations of elacytarabine in the ovarian cancer indication are not warranted.
 
 
 
 
	Content Type Journal ArticleCategory Clinical Trial ReportPages 1-7DOI 10.1007/s00280-011-1735-4Authors
		S. Pignata, Istituto Nazionale Tumori, IRCCS “Fondazione G. Pascale”, Naples, EU, ItalyF. Amant, Leuven Cancer Institute, Gynaecological Oncology, Leuven, BelgiumG. Scambia, Università Cattolica del Sacro Cuore, Rome, ItalyR. Sorio, Centro di Rifer...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5207903</comments>
            <pubDate>Fri, 09 Sep 2011 16:46:16 +0100</pubDate>
            <guid isPermaLink="false">5207903</guid>        </item>
        <item>
            <title>A phase I study of 5-azacytidine and erlotinib in advanced solid tumor malignancies</title>
            <link>http://www.medworm.com/index.php?rid=5207904&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fe2p7264j5h82n51t%2F</link>
            <description>Conclusion&amp;nbsp;&amp;nbsp;The combination of erlotinib and 5-azacytidine was well tolerated with interesting clinical activity in lung, head and neck,
 and ovarian cancer. The recommended dose for phase II study is erlotinib 150&amp;nbsp;mg daily and 5-azacytidine 75 mg/m2 daily on days 1–4 and 15–18 of a 28-day cycle.
 
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-8DOI 10.1007/s00280-011-1729-2Authors
		Julie Bauman, Division of Hematology/Oncology, University of New Mexico Cancer Center, Albuquerque, NM, USAClaire Verschraegen, Division of Hematology/Oncology, University of Vermont, Burlington, VT, USASteven Belinsky, Lovelace Respiratory Research Institute, Lung Cancer Program, Albuquerque, NM, USACarolyn Muller, Division of Gynecology Oncology, University of New Mexi...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5207904</comments>
            <pubDate>Thu, 08 Sep 2011 06:10:50 +0100</pubDate>
            <guid isPermaLink="false">5207904</guid>        </item>
        <item>
            <title>Triple-negative phenotype is of adverse prognostic value in patients treated with dose-dense sequential adjuvant chemotherapy: a translational research analysis in the context of a Hellenic Cooperative Oncology Group (HeCOG) randomized phase III trial</title>
            <link>http://www.medworm.com/index.php?rid=5207905&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F67838739r664lh67%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;The results of this study confirm that triple negative, luminal B and HER2-enriched phenotypes identified by IHC are of adverse
 prognostic value in high-risk breast cancer patients treated with dose-dense sequential adjuvant chemotherapy.
 
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-14DOI 10.1007/s00280-011-1730-9Authors
		P. Skarlos, Department of Radiotherapy, Agios Savvas Cancer Hospital, Athens, GreeceC. Christodoulou, Second Department of Medical Oncology, Metropolitan Hospital, Piraeus, GreeceK. T. Kalogeras, Translational Research Section, Hellenic Cooperative Oncology Group, Data Office, Athens, GreeceA. G. Eleftheraki, Section of Biostatistics, Hellenic Cooperative Oncology Group, Data Office, Athens, GreeceM. Bobos, Laboratory of M...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5207905</comments>
            <pubDate>Thu, 08 Sep 2011 06:10:49 +0100</pubDate>
            <guid isPermaLink="false">5207905</guid>        </item>
        <item>
            <title>Phase I dose escalation study of KOS-1584, a novel epothilone, in patients with advanced solid tumors</title>
            <link>http://www.medworm.com/index.php?rid=5175469&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F28088745g313773h%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;The RP2D of KOS-1584 is 36&amp;nbsp;mg/m2. The lack of severe neurologic toxicity, diarrhea, neutropenia, or hypersensitivity reactions; favorable pharmacokinetic
 profile; and early evidence of activity support further evaluation.
 
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-9DOI 10.1007/s00280-011-1724-7Authors
		Elaine T. Lam, The Ohio State University Comprehensive Cancer Center, Columbus, OH, USASanjay Goel, Montefiore-Einstein Center for Cancer Care, Bronx, NY, USALarry J. Schaaf, The Ohio State University Comprehensive Cancer Center, Columbus, OH, USAGillian F. Cropp, Kosan Biosciences, Inc., Hayward, CA, USAAlison L. Hannah, Kosan Biosciences, Inc., Hayward, CA, USAYiqing Zhou, Kosan Biosciences, Inc., Hayward, CA, USABarbara McCracken, T...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5175469</comments>
            <pubDate>Fri, 26 Aug 2011 16:16:34 +0100</pubDate>
            <guid isPermaLink="false">5175469</guid>        </item>
        <item>
            <title>An all-oral combination of metronomic cyclophosphamide plus capecitabine in patients with anthracycline- and taxane-pretreated metastatic breast cancer: a phase II study</title>
            <link>http://www.medworm.com/index.php?rid=5175470&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F172138722471273h%2F</link>
            <description>Conclusion&amp;nbsp;&amp;nbsp;The all-oral combination of metronomic CTX plus capecitabine is an effective and convenient and well-tolerated regimen for
 MBC. (ClinicalTrials.gov number, NCT00589901).
 
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-8DOI 10.1007/s00280-011-1728-3Authors
		Zhonghua Wang, Department of Medical Oncology, Cancer Hospital of Fudan University, Shanghai Medical College, 270 Dongan Road, Shanghai, 200032 ChinaJingsong Lu, Department of Breast Surgery, Cancer Hospital of Fudan University, Shanghai Medical College, Shanghai, ChinaShiangjiin Leaw, Department of Medical Oncology, Cancer Hospital of Fudan University, Shanghai Medical College, 270 Dongan Road, Shanghai, 200032 ChinaXiaonan Hong, Department of Medical Oncology, Cancer Hospital of Fudan Unive...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5175470</comments>
            <pubDate>Fri, 26 Aug 2011 16:16:33 +0100</pubDate>
            <guid isPermaLink="false">5175470</guid>        </item>
        <item>
            <title>The effect of thalidomide on the pharmacokinetics of irinotecan and metabolites in advanced solid tumor patients</title>
            <link>http://www.medworm.com/index.php?rid=5161031&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F473215v5k1833t53%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;This study did not find any clinically meaningful effects of thalidomide on the pharmacokinetics of irinotecan or its metabolites.
 
 
 
	Content Type Journal ArticleCategory Short CommunicationPages 1-4DOI 10.1007/s00280-011-1727-4Authors
		Jacqueline Ramírez, Department of Medicine, Section of Hematology/Oncology, University of Chicago, 5841 S. Maryland Avenue, MC2115, Chicago, IL 60637, USAKehua Wu, Department of Medicine, Section of Hematology/Oncology, University of Chicago, 5841 S. Maryland Avenue, MC2115, Chicago, IL 60637, USALinda Janisch, Department of Medicine, Section of Hematology/Oncology, University of Chicago, 5841 S. Maryland Avenue, MC2115, Chicago, IL 60637, USATheodore Karrison, Department of Health Studies, University of Chicago, Chicago, IL 606...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5161031</comments>
            <pubDate>Mon, 22 Aug 2011 16:00:16 +0100</pubDate>
            <guid isPermaLink="false">5161031</guid>        </item>
        <item>
            <title>Probenecid is a chemosensitizer in cancer cell lines</title>
            <link>http://www.medworm.com/index.php?rid=5161030&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fc72u81333223u15p%2F</link>
            <description>In this study,
 we tested in vitro co-administration of the antineoplastic agents cisplatin or paclitaxel with probenecid, an anion channel
 inhibitor, in a panel of cancer cell lines to determine the cytotoxicity and synergistic effects of these drug combinations.
 In addition, we measured the clonogenicity and apoptotic index in these cells. We observed a synergistic interaction between
 probenecid and the chemotherapeutic agents, and increasing doses of probenecid resulted in a significant decrease in the effective
 doses of the chemotherapeutic agents. For the antineoplastic agent and probenecid combinations, we found increased cell death,
 reduced colony formation, and a higher number of apoptotic cells, compared with treatment of cisplatin or paclitaxel alone.
 Further research is ne...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5161030</comments>
            <pubDate>Mon, 22 Aug 2011 16:00:16 +0100</pubDate>
            <guid isPermaLink="false">5161030</guid>        </item>
        <item>
            <title>Docetaxel plus gemcitabine in combination with capecitabine as treatment for inoperable pancreatic cancer: a phase II study</title>
            <link>http://www.medworm.com/index.php?rid=5161032&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ft37k2t6x2210q313%2F</link>
            <description>Conclusion&amp;nbsp;&amp;nbsp;The combination of gemcitabine with docetaxel and capecitabine is feasible and exhibits satisfactory degree of activity in
 patients with advanced pancreatic cancer, deserving further exploration.
 
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-8DOI 10.1007/s00280-011-1717-6Authors
		N. Xenidis, Department of Medical Oncology, University General Hospital of Alexandroupolis, Dragana, 68100 Alexandroupolis, Thrace, GreeceL. Chelis, Department of Medical Oncology, University General Hospital of Alexandroupolis, Dragana, 68100 Alexandroupolis, Thrace, GreeceK. Amarantidis, Department of Medical Oncology, University General Hospital of Alexandroupolis, Dragana, 68100 Alexandroupolis, Thrace, GreeceE. Chamalidou, Department of Medical Oncology, Univers...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5161032</comments>
            <pubDate>Fri, 19 Aug 2011 15:53:06 +0100</pubDate>
            <guid isPermaLink="false">5161032</guid>        </item>
        <item>
            <title>Phase I and pharmacokinetic study of nab-paclitaxel, nanoparticle albumin-bound paclitaxel, administered weekly to Japanese patients with solid tumors and metastatic breast cancer</title>
            <link>http://www.medworm.com/index.php?rid=5161034&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fk762133551x50273%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;Weekly administration of nab-paclitaxel was well tolerated up to 100&amp;nbsp;mg/m2 by heavily pretreated patients. For MBC patients, 150&amp;nbsp;mg/m2 nab-paclitaxel as a first-line therapy was well tolerated. Dose reduction due to neuropathy allows multiple cycles of treatment.
 
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-9DOI 10.1007/s00280-011-1726-5Authors
		Masashi Ando, Department of Breast and Medical Oncology, National Cancer Center Hospital, Tsukiji 5-1-1, Chuo-ku, Tokyo, 104-0045 JapanKan Yonemori, Department of Breast and Medical Oncology, National Cancer Center Hospital, Tsukiji 5-1-1, Chuo-ku, Tokyo, 104-0045 JapanNoriyuki Katsumata, Department of Breast and Medical Oncology, National Cancer Center Hospital, Tsukiji 5-1-1, Chuo-ku, Tok...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5161034</comments>
            <pubDate>Fri, 19 Aug 2011 06:40:43 +0100</pubDate>
            <guid isPermaLink="false">5161034</guid>        </item>
        <item>
            <title>Phase I study of cediranib in combination with cisplatin plus fluoropyrimidine (S-1 or capecitabine) in Japanese patients with previously untreated advanced gastric cancer</title>
            <link>http://www.medworm.com/index.php?rid=5161033&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fu56q628522322033%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;Cediranib 20&amp;nbsp;mg/day in combination with cisplatin and S-1 or capecitabine was tolerable, with no new toxicities identified,
 and showed preliminary evidence of antitumour activity.
 
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-8DOI 10.1007/s00280-011-1723-8Authors
		Taroh Satoh, Kinki University School of Medicine, Osaka, JapanYasuhide Yamada, National Cancer Centre Hospital, Tokyo, JapanKei Muro, Aichi Cancer Centre Hospital, Aichi, JapanHidetoshi Hayashi, Kinki University School of Medicine, Osaka, JapanYasuhiro Shimada, National Cancer Centre Hospital, Tokyo, JapanDaisuke Takahari, Aichi Cancer Centre Hospital, Aichi, JapanKeisei Taku, Shizuoka Cancer Centre, Shizuoka, JapanTakako Eguchi Nakajima, St. Marianna University School of Medi...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5161033</comments>
            <pubDate>Fri, 19 Aug 2011 06:40:43 +0100</pubDate>
            <guid isPermaLink="false">5161033</guid>        </item>
        <item>
            <title>The use of GTX as second-line and later chemotherapy for metastatic pancreatic cancer: a retrospective analysis</title>
            <link>http://www.medworm.com/index.php?rid=5161035&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fg1537814p2647ppr%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;GTX is an active regimen in patients previously treated with gemcitabine for mPC. Better performance status and &amp;gt;75% drop
 in pretreatment CA 19-9 were associated with longer survival. The number of prior regimens did not predict for survival duration.
 
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-6DOI 10.1007/s00280-011-1705-xAuthors
		Hassan K. Dakik, Duke University Medical Center, Durham, NC, USADaniel J. Moskovic, Baylor College of Medicine, Houston, TX, USAPeter J. Carlson, Baylor College of Medicine, Houston, TX, USAEric P. Tamm, The University of Texas MD Anderson Cancer Center, 1515 Holcombe Blvd. Unit 426, Houston, TX 77030, USAWei Qiao, The University of Texas MD Anderson Cancer Center, 1515 Holcombe Blvd. Unit 426, Houston, TX 7...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5161035</comments>
            <pubDate>Thu, 18 Aug 2011 05:59:58 +0100</pubDate>
            <guid isPermaLink="false">5161035</guid>        </item>
        <item>
            <title>Pharmacokinetics of trabectedin on hemodialysis: an application for the management of cancer patients with end-stage renal disease</title>
            <link>http://www.medworm.com/index.php?rid=5161037&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fx238l774h8007571%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;This case reports for the first time the feasibility of trabectedin therapy in a hemodialyzed patient. Given the rising incidence
 of cancer in patients with end-stage renal disease, it is crucial to provide data that improve the management of anticancer
 drugs in dialyzed patients.
 
 
 
 
	Content Type Journal ArticleCategory Short CommunicationPages 1-5DOI 10.1007/s00280-011-1718-5Authors
		Juliette Thariat, Department of Radiation Oncology/IBDC CNRS 6543, Centre Antoine Lacassagne, 33 Av. de Valombrose, 06189 Nice Cedex 2, FranceMarie-Christine Etienne-Grimaldi, Oncopharmacology Unit, EA 3836, Centre Antoine Lacassagne, Nice, FranceVincent Launay-Vacher, Service ICAR, Department of Nephrology, Hôpital Pitié-Salpetrière, Paris, FranceArturo Soto-Matos, Clinical...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5161037</comments>
            <pubDate>Thu, 18 Aug 2011 05:59:55 +0100</pubDate>
            <guid isPermaLink="false">5161037</guid>        </item>
        <item>
            <title>A phase I study of bortezomib and temozolomide in patients with advanced solid tumors</title>
            <link>http://www.medworm.com/index.php?rid=5161036&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F72j4071277484np6%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;The MTDs for the combination of bortezomib and temozolomide in patients not taking HEIAs are 1.3 and 200&amp;nbsp;mg/m2, respectively. The rate of bortezomib elimination in patients taking HEIAs was increased twofold. Additional trials are needed
 to better define the optimal dosing in such patients.
 
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-10DOI 10.1007/s00280-011-1721-xAuthors
		J. Portnow, Department of Medical Oncology, City of Hope, 1500 East Duarte Road, Duarte, CA 91030, USAP. Frankel, Department of Medical Oncology, City of Hope, 1500 East Duarte Road, Duarte, CA 91030, USAS. Koehler, Department of Medical Oncology, City of Hope, 1500 East Duarte Road, Duarte, CA 91030, USAP. Twardowski, Department of Medical Oncology, City of Hope, 1...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5161036</comments>
            <pubDate>Thu, 18 Aug 2011 05:59:55 +0100</pubDate>
            <guid isPermaLink="false">5161036</guid>        </item>
        <item>
            <title>Reply</title>
            <link>http://www.medworm.com/index.php?rid=5131706&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fp556328245421pgu%2F</link>
            <description>Content Type Journal ArticlePages 1-1DOI 10.1007/s00280-011-1720-yAuthors
		Velia D’Angelo, Naples, Italy
	

	
		Journal Cancer Chemotherapy and PharmacologyOnline ISSN 1432-0843Print ISSN 0344-5704 (Source: Cancer Chemotherapy and Pharmacology)</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5131706</comments>
            <pubDate>Sat, 13 Aug 2011 06:15:37 +0100</pubDate>
            <guid isPermaLink="false">5131706</guid>        </item>
        <item>
            <title>Nrf2 knockdown by shRNA inhibits tumor growth and increases efficacy of chemotherapy in cervical cancer</title>
            <link>http://www.medworm.com/index.php?rid=5131705&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fy1k74t5883v6h737%2F</link>
            <description>Conclusion&amp;nbsp;&amp;nbsp;Our findings provide evidence that the inhibition of Nrf2 activity by shRNA might be a promising therapeutic strategy to enhance
 the efficacy of anticancer drugs and thus can be applied further during the course of chemotherapy in the treatment of cervical
 cancer.
 
 
 
 
	Content Type Journal ArticlePages 1-10DOI 10.1007/s00280-011-1722-9Authors
		Xiangdong Ma, Department of Obstetrics and Gynecology, Xijing Hospital, Fourth Military Medical University, 17 Changle West Road, Xi’an, 710032 People’s Republic of ChinaJianfang Zhang, Department of Obstetrics and Gynecology, Xijing Hospital, Fourth Military Medical University, 17 Changle West Road, Xi’an, 710032 People’s Republic of ChinaShujuan Liu, Department of Obstetrics and Gynecology, Xijing Hospital, Four...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5131705</comments>
            <pubDate>Sat, 13 Aug 2011 06:15:37 +0100</pubDate>
            <guid isPermaLink="false">5131705</guid>        </item>
        <item>
            <title>Severe fluoropyrimidine-related toxicity: clinical implications of DPYD analysis and UH2/U ratio evaluation</title>
            <link>http://www.medworm.com/index.php?rid=5131707&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F81g1277pqg542258%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The fluoropyrimidines are commonly used in chemotherapeutic cancer medicine, but many patients still experience severe adverse
 side effects from these drugs. We observed a severe toxicity in a 50-year-old woman treated with capecitabine and docetaxel
 for a metastatic breast cancer. Since dihydropyrimidine dehydrogenase (DPD) is the main candidate for pharmacogenetic studies
 on 5-FU toxicity, the entire coding sequence and exon-flanking intronic regions of the DPYD gene were sequenced in the patient. None of the previously described deleterious variants were detected. Also, the haplotype-based
 analysis failed to reveal DPYD variations associated with 5-FU toxicity. We also evaluated the UH2/U ratio in plasma as an index of 5-FU pharmacokinetics.
 The UH2/U value did ...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5131707</comments>
            <pubDate>Thu, 11 Aug 2011 05:54:10 +0100</pubDate>
            <guid isPermaLink="false">5131707</guid>        </item>
        <item>
            <title>MTHFR 677TT genotype and toxicity of methotrexate: controversial results</title>
            <link>http://www.medworm.com/index.php?rid=5108968&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fxu2432m2g6h701wr%2F</link>
            <description>Content Type Journal ArticlePages 1-2DOI 10.1007/s00280-011-1719-4Authors
		Elixabet Lopez–Lopez, Department of Genetics, Physic Anthropology and Animal Physiology, Faculty of Medicine and Dentistry, University of the Basque Country, Barrio Sarriena s/n, 48940 Leioa, SpainJavier Ballesteros, Department of Neurosciences, University of the Basque Country, Leioa, SpainAfrica Garcia-Orad, Department of Genetics, Physic Anthropology and Animal Physiology, Faculty of Medicine and Dentistry, University of the Basque Country, Barrio Sarriena s/n, 48940 Leioa, Spain
	

	
		Journal Cancer Chemotherapy and PharmacologyOnline ISSN 1432-0843Print ISSN 0344-5704 (Source: Cancer Chemotherapy and Pharmacology)</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5108968</comments>
            <pubDate>Sat, 06 Aug 2011 05:46:55 +0100</pubDate>
            <guid isPermaLink="false">5108968</guid>        </item>
        <item>
            <title>Nucleoside transporters are widely expressed in ovarian carcinoma effusions</title>
            <link>http://www.medworm.com/index.php?rid=5108969&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fnj47762228524h16%2F</link>
            <description>Conclusion&amp;nbsp;&amp;nbsp;Nucleoside transporters are frequently expressed in ovarian carcinoma effusions, but their expression generally appears to
 be unrelated to chemoresponse in this cancer in a cohort of patients treated by platinum-based chemotherapy. The role of ENT2
 as a prognostic marker in this disease, as well as the role of these molecules in determining chemoresponse in patients treated
 by nucleoside analogs, merits further research.
 
 
 
 
	Content Type Journal ArticlePages 1-9DOI 10.1007/s00280-011-1716-7Authors
		Annika J. Bock, Department of Pathology, Oslo University Hospital, Norwegian Radium Hospital, Montebello, 0424 Oslo, NorwayHiep Phuc Dong, Department of Pathology, Oslo University Hospital, Norwegian Radium Hospital, Montebello, 0424 Oslo, NorwayClaes G. Tropé, De...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5108969</comments>
            <pubDate>Sat, 06 Aug 2011 05:46:54 +0100</pubDate>
            <guid isPermaLink="false">5108969</guid>        </item>
        <item>
            <title>Dose adaptation of capecitabine based on individual prediction of limiting toxicity grade: evaluation by clinical trial simulation</title>
            <link>http://www.medworm.com/index.php?rid=5103736&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fr8738l0195724586%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;These results indicate that individual prediction-based dose adaptation based on ordinal data may be feasible and beneficial.
 
 
 
	Content Type Journal ArticlePages 1-9DOI 10.1007/s00280-011-1714-9Authors
		Ines Paule, Université de Lyon, 69622 Lyon, FranceMichel Tod, Université de Lyon, 69622 Lyon, FranceEmilie Hénin, Université de Lyon, 69622 Lyon, FranceBenoit You, Université de Lyon, 69622 Lyon, FranceGilles Freyer, Université de Lyon, 69622 Lyon, FrancePascal Girard, Université de Lyon, 69622 Lyon, France
	

	
		Journal Cancer Chemotherapy and PharmacologyOnline ISSN 1432-0843Print ISSN 0344-5704 (Source: Cancer Chemotherapy and Pharmacology)</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5103736</comments>
            <pubDate>Tue, 02 Aug 2011 06:17:28 +0100</pubDate>
            <guid isPermaLink="false">5103736</guid>        </item>
        <item>
            <title>Interaction potential of the endothelin-A receptor antagonist atrasentan with drug transporters and drug-metabolising enzymes assessed in vitro</title>
            <link>http://www.medworm.com/index.php?rid=5087235&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fn31567880v0m4867%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;Our data provide a comprehensive analysis of the induction profile of atrasentan and its interaction with P-gp and BCRP. The
 profound induction effects stress the need for thorough assessment of its interaction potential in vivo.
 
 
 
 
	Content Type Journal ArticlePages 1-6DOI 10.1007/s00280-011-1715-8Authors
		Johanna Weiss, Department of Clinical Pharmacology and Pharmacoepidemiology, University of Heidelberg, Im Neuenheimer Feld 410, 69120 Heidelberg, GermanyWalter Emil Haefeli, Department of Clinical Pharmacology and Pharmacoepidemiology, University of Heidelberg, Im Neuenheimer Feld 410, 69120 Heidelberg, Germany
	

	
		Journal Cancer Chemotherapy and PharmacologyOnline ISSN 1432-0843Print ISSN 0344-5704 (Source: Cancer Chemotherapy and Pharmacology)</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5087235</comments>
            <pubDate>Sat, 30 Jul 2011 15:53:05 +0100</pubDate>
            <guid isPermaLink="false">5087235</guid>        </item>
        <item>
            <title>Phase I study of the synthetic triterpenoid, 2-cyano-3, 12-dioxoolean-1, 9-dien-28-oic acid (CDDO), in advanced solid tumors</title>
            <link>http://www.medworm.com/index.php?rid=5087236&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fw74h54v222328853%2F</link>
            <description>Conclusion&amp;nbsp;&amp;nbsp;A causal relationship of observed thromboembolic events to CDDO was considered possible but could not be established.
 
 
 
	Content Type Journal ArticlePages 1-8DOI 10.1007/s00280-011-1712-yAuthors
		Giovanna Speranza, Division of Cancer Treatment and Diagnosis, National Cancer Institute, Bethesda, MD, USAMartin E. Gutierrez, Center for Cancer Research, National Cancer Institute, Bethesda, MD, USAShivaani Kummar, Division of Cancer Treatment and Diagnosis, National Cancer Institute, Bethesda, MD, USAJohn M. Strong, Laboratory of Clinical Pharmacology, Center for Drug Evaluation and Research, Food and Drug Administration, Silver Spring, MD, USARobert J. Parker, Laboratory of Clinical Pharmacology, Center for Drug Evaluation and Research, Food and Drug Administration, ...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5087236</comments>
            <pubDate>Sat, 30 Jul 2011 15:53:04 +0100</pubDate>
            <guid isPermaLink="false">5087236</guid>        </item>
        <item>
            <title>A multicenter analysis of GTX chemotherapy in patients with locally advanced and metastatic pancreatic adenocarcinoma</title>
            <link>http://www.medworm.com/index.php?rid=5087237&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Few4625l134605541%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;We observe a substantial survival benefit with GTX chemotherapy in our cohort of patients with advanced pancreatic cancer.
 These findings warrant further investigation of this combination in this patient population.
 
 
 
 
	Content Type Journal ArticlePages 1-10DOI 10.1007/s00280-011-1704-yAuthors
		Ana De Jesus-Acosta, Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins, 1650 Orleans Street, CRB I, Room 590, Baltimore, MD 21231, USAGeorge R. Oliver, Cancer Institute of Dallas, Duncanville, TX 75137, USAAmanda Blackford, Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins, 1650 Orleans Street, CRB I, Room 590, Baltimore, MD 21231, USAKatharine Kinsman, Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins, 1650 Orleans Street, CRB I, Room 590, Ba...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5087237</comments>
            <pubDate>Thu, 28 Jul 2011 15:59:07 +0100</pubDate>
            <guid isPermaLink="false">5087237</guid>        </item>
        <item>
            <title>A multicenter phase II study of combined chemotherapy with docetaxel, cisplatin, and S-1 in patients with unresectable or recurrent gastric cancer (KDOG 0601)</title>
            <link>http://www.medworm.com/index.php?rid=5087238&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F968376001437n173%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;Triplet of docetaxel, cisplatin, and S-1 is a well-tolerated and highly active regimen for advanced or recurrent gastric cancer.
 A 60&amp;nbsp;mg/m2 of cisplatin is as effective as 70&amp;nbsp;mg/m2 of cisplatin.
 
 
 
 
	Content Type Journal ArticlePages 1-7DOI 10.1007/s00280-011-1701-1Authors
		Wasaburo Koizumi, Department of Gastroenterology/Gastrointestinal Oncology, Kitasato University East Hospital, 2-1-1 Asamizodai, Sagamihara, Kanagawa, 228-8520 JapanNorisuke Nakayama, Division of Gastroenterology, Kanagawa Cancer Center, Kanagawa, JapanSatoshi Tanabe, Department of Gastroenterology/Gastrointestinal Oncology, Kitasato University East Hospital, 2-1-1 Asamizodai, Sagamihara, Kanagawa, 228-8520 JapanTohru Sasaki, Department of Gastroenterology/Gastrointestinal Oncology...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5087238</comments>
            <pubDate>Wed, 27 Jul 2011 18:48:26 +0100</pubDate>
            <guid isPermaLink="false">5087238</guid>        </item>
        <item>
            <title>Physiologically based pharmacokinetic modelling of high- and low-dose etoposide: from adults to children</title>
            <link>http://www.medworm.com/index.php?rid=5087239&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F01x53316555207t8%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;The PBPK model matched the pharmacokinetics in different dosing regimens in adults. Furthermore, the scaling procedure from
 the adult model to children provides useful predictions for paediatric patients. Comedication with drugs influencing the metabolism
 and excretion has to be taken into account. This approach could be useful for planning pharmacokinetic studies in children.
 
 
 
 
	Content Type Journal ArticlePages 1-9DOI 10.1007/s00280-011-1706-9Authors
		Gisela Kersting, Department of Pharmaceutical and Medical Chemistry, Clinical Pharmacy, University of Münster, Münster, GermanyStefan Willmann, Bayer Technology Services GmbH, Competence Centre Systems Biology and Computational Solutions, 51368 Leverkusen, GermanyGudrun Würthwein, Centre for Clinical Trial...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5087239</comments>
            <pubDate>Tue, 26 Jul 2011 05:47:45 +0100</pubDate>
            <guid isPermaLink="false">5087239</guid>        </item>
        <item>
            <title>Oral fludarabine in combination with doxorubicin and dexamethasone as first-line therapy for nodal peripheral T-cell lymphomas: early results of a prospective multicenter study</title>
            <link>http://www.medworm.com/index.php?rid=5087240&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fp2rv0146t821300t%2F</link>
            <description>Conclusion&amp;nbsp;&amp;nbsp;The FAD regimen had encouraging efficacy with an acceptable toxicity profile in patients with nodal PTCLs.
 
 
 
	Content Type Journal ArticlePages 1-9DOI 10.1007/s00280-011-1711-zAuthors
		Xiao-Jian Liu, Department of Medical Oncology, Fudan University Shanghai Cancer center, 270 Dong-An Road, Shanghai, 200032 People’s Republic of ChinaYe Guo, Department of Medical Oncology, Fudan University Shanghai Cancer center, 270 Dong-An Road, Shanghai, 200032 People’s Republic of ChinaYun Fan, Department of Oncology, Zhejiang Provincial Cancer Hospital, 38 Guangji Road, Hangzhou, 310022 People’s Republic of ChinaKang-Sheng Gu, Department of Medical Oncology, The First Affiliated Hospital of Anhui Medical University, 218 Jixi Road, Hefei, 230022 People’s Republic of Chi...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5087240</comments>
            <pubDate>Tue, 26 Jul 2011 05:47:44 +0100</pubDate>
            <guid isPermaLink="false">5087240</guid>        </item>
        <item>
            <title>Inhibition of glutathione synthesis reverses Krüppel-like factor 4-mediated cisplatin resistance</title>
            <link>http://www.medworm.com/index.php?rid=5063315&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fb30x5407777155k4%2F</link>
            <description>Conclusion&amp;nbsp;&amp;nbsp;We conclude that KLF4 regulates the cellular sensitivity to cisplatin in hepatocarcinoma stem-like cells and hepatocarcinoma
 cells by elevating intracellular glutathione levels.
 
 
 
 
	Content Type Journal ArticlePages 1-9DOI 10.1007/s00280-011-1708-7Authors
		Yongsheng Jia, Graduate School, Peking Union Medical College, Chinese Academy of Medical Sciences, Beijing, 100730 People’s Republic of ChinaWenjian Zhang, Institute of Clinical Medical Sciences, China–Japan Friendship Hospital, 2 East Yinghuayuan Street, Beijing, 100029 People’s Republic of ChinaHonglin Liu, Institute of Clinical Medical Sciences, China–Japan Friendship Hospital, 2 East Yinghuayuan Street, Beijing, 100029 People’s Republic of ChinaLiang Peng, Institute of Clinical Medical Sciences,...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5063315</comments>
            <pubDate>Thu, 21 Jul 2011 18:13:27 +0100</pubDate>
            <guid isPermaLink="false">5063315</guid>        </item>
        <item>
            <title>A randomised phase II trial of two sequential schedules of docetaxel and cisplatin followed by gemcitabine in patients with advanced non-small-cell lung cancer</title>
            <link>http://www.medworm.com/index.php?rid=5063314&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fk816r02g26vn8221%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;Our data demonstrate the feasibility of a sequential approach of cisplatin plus docetaxel followed by single-agent gemcitabine.
 Weekly administration of platinum-docetaxel is associated with an improved safety profile but lower efficacy than the conventional
 three-weekly schedule (registration ID 2004-001044-72).
 
 
 
 
	Content Type Journal ArticlePages 1-7DOI 10.1007/s00280-011-1710-0Authors
		Francesco Grossi, Istituto Nazionale per la Ricerca sul Cancro, S.S. Tumori Polmonari, Largo R. Benzi, 10, 16132 Genoa, ItalyFilippo de Marinis, Ospedale S. Camillo Forlanini, Rome, ItalyVittorio Gebbia, Casa di Cura La Maddalena, Palermo, ItalyFerdinando Riccardi, Ospedale Cardarelli, Naples, ItalyOrazio Caffo, Ospedale S. Chiara, Trento, ItalyTeresa Gamucci, P.O. SS. Tri...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5063314</comments>
            <pubDate>Thu, 21 Jul 2011 18:13:27 +0100</pubDate>
            <guid isPermaLink="false">5063314</guid>        </item>
        <item>
            <title>Phase II clinical trial evaluating docetaxel, vinorelbine and GM-CSF in stage IV melanoma</title>
            <link>http://www.medworm.com/index.php?rid=5063316&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fg58qr8r07380121k%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;The DVS regimen was active in patients with advanced, previously treated melanoma, with manageable toxicity. The favorable
 1-year overall survival and median survival rates suggest that further evaluation of the DVS regimen is warranted.
 
 
 
 
	Content Type Journal ArticlePages 1-7DOI 10.1007/s00280-011-1703-zAuthors
		Zeynep Eroglu, Departments of Medicine, University of California Irvine Medical Center, Orange, CA 92868, USAKevin M. Kong, Departments of Medicine, University of California Irvine Medical Center, Orange, CA 92868, USAJames G. Jakowatz, Departments of Surgery, University of California Irvine Medical Center, Orange, CA 92868, USAWolfram Samlowski, Nevada Cancer Institute, Las Vegas, NV 89135, USAJohn P. Fruehauf, Departments of Medicine, University o...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5063316</comments>
            <pubDate>Tue, 19 Jul 2011 05:49:25 +0100</pubDate>
            <guid isPermaLink="false">5063316</guid>        </item>
        <item>
            <title>Doxorubicin and ifosfamide for high-grade sarcoma during pregnancy</title>
            <link>http://www.medworm.com/index.php?rid=5063317&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ff4710ppx21k3j133%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;In view of this single-centre experience, we suggest that the treatment of high-grade sarcoma during the third trimester of
 pregnancy should include an adapted regimen tailored to the pharmacological specificities of the pregnant patients.
 
 
 
 
	Content Type Journal ArticlePages 1-11DOI 10.1007/s00280-011-1707-8Authors
		Olivier Mir, Department of Medicine, Sarcoma Unit, Herault Ward, Institut Gustave Roussy, Paris Sud University, 39, rue Camille Desmoulins, 94800 Villejuif cedex, FranceNarjiss Berrada, Department of Medicine, Sarcoma Unit, Herault Ward, Institut Gustave Roussy, Paris Sud University, 39, rue Camille Desmoulins, 94800 Villejuif cedex, FranceJulien Domont, Department of Medicine, Sarcoma Unit, Herault Ward, Institut Gustave Roussy, Paris Sud Univer...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5063317</comments>
            <pubDate>Tue, 19 Jul 2011 05:49:24 +0100</pubDate>
            <guid isPermaLink="false">5063317</guid>        </item>
        <item>
            <title>Phase I trial examining addition of gemcitabine to CHOP in intermediate grade NHL</title>
            <link>http://www.medworm.com/index.php?rid=5038056&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ff14vn2l5084012l2%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;This Phase I trial concludes that gemcitabine 500&amp;nbsp;mg/m2 on days 1 and 4 of each 21-day cycle is the maximum tolerated dose when combined with standard CHOP chemotherapy with G-CSF
 support for intermediate grade NHL.
 
 
 
 
	Content Type Journal ArticlePages 1-6DOI 10.1007/s00280-011-1702-0Authors
		John L. Reagan, Department of Hematology/Oncology, The Miriam Hospital, 164 Summit Avenue, Providence, RI 02906, USAAlan Rosmarin, Department of Hematology/Oncology, The Miriam Hospital, 164 Summit Avenue, Providence, RI 02906, USAJames N. Butera, Department of Hematology/Oncology, The Miriam Hospital, 164 Summit Avenue, Providence, RI 02906, USAAhmed Nadeem, Department of Hematology/Oncology, The Miriam Hospital, 164 Summit Avenue, Providence, RI 02906, USAFred J. ...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5038056</comments>
            <pubDate>Thu, 14 Jul 2011 16:52:00 +0100</pubDate>
            <guid isPermaLink="false">5038056</guid>        </item>
        <item>
            <title>Chemotherapy with gemcitabine, cisplatin, and docetaxel in the treatment for patients with muscle-invasive bladder cancer: a multicenter phase II study of the Hellenic Oncology Research Group (HORG)</title>
            <link>http://www.medworm.com/index.php?rid=5030060&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F97jv2723604278j6%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;The GCD combination is an active and well-tolerated regimen in patients with chemotherapy-naive locally advanced or metastatic
 TCC and merits to be further investigated.
 
 
 
 
	Content Type Journal ArticlePages 1-6DOI 10.1007/s00280-011-1694-9Authors
		Ioannis Boukovinas, Hellenic Oncology Research Group (HORG), 55 Lomvardou str, 11740 Athens, GreeceNikolaos Androulakis, Hellenic Oncology Research Group (HORG), 55 Lomvardou str, 11740 Athens, GreeceNikolaos Kentepozidis, Hellenic Oncology Research Group (HORG), 55 Lomvardou str, 11740 Athens, GreeceAris Polyzos, Hellenic Oncology Research Group (HORG), 55 Lomvardou str, 11740 Athens, GreecePavlos Papakotoulas, Hellenic Oncology Research Group (HORG), 55 Lomvardou str, 11740 Athens, GreeceNikolaos Ziras, Hellenic O...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5030060</comments>
            <pubDate>Tue, 12 Jul 2011 06:04:23 +0100</pubDate>
            <guid isPermaLink="false">5030060</guid>        </item>
        <item>
            <title>Effect of trabectedin on the QT interval in patients with advanced solid tumor malignancies</title>
            <link>http://www.medworm.com/index.php?rid=5020065&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fc15465gn0wp66112%2F</link>
            <description>Conclusion&amp;nbsp;&amp;nbsp;Trabectedin did not prolong the QTc interval. Safety and pharmacokinetic profiles of trabectedin were similar to that observed
 in other ovarian and breast cancer studies.
 
 
 
 
	Content Type Journal ArticlePages 1-10DOI 10.1007/s00280-011-1697-6Authors
		R. Thertulien, Cancer Centers of North Carolina-Asheville, 20 Medical Park Drive, Asheville, NC 28803, USAG. M. Manikhas, City Clinical Oncology Dispensary, St. Petersburg, RussiaL. Y. Dirix, AZ Sint-Augustinus, Oncologisch Centrum, Wilrijk, BelgiumJ. B. Vermorken, Universitair Ziekenhuis Antwerpen, Edegem, BelgiumK. Park, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, KoreaM. M. Jain, Ruby Hall Clinic, Pune, IndiaJ. J. Jiao, Johnson &amp; Johnson Pharmaceutical Research &amp; Development, L.L.C...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5020065</comments>
            <pubDate>Fri, 08 Jul 2011 06:29:08 +0100</pubDate>
            <guid isPermaLink="false">5020065</guid>        </item>
        <item>
            <title>Phase IB study of sorafenib in combination with gemcitabine and cisplatin in patients with refractory solid tumors</title>
            <link>http://www.medworm.com/index.php?rid=5020066&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F0772l14522836562%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;Sorafenib as continuous oral treatment in combination with gemcitabine and cisplatin demonstrated an acceptable safety profile.
 No clinically relevant pharmacokinetic interaction was detected. Preliminary antitumor activity, pharmacokinetic, and safety
 data support the recommendation of 400&amp;nbsp;mg sorafenib twice daily in combination with cisplatin and gemcitabine to be further
 evaluated in clinical studies.
 
 
 
 
	Content Type Journal ArticlePages 1-7DOI 10.1007/s00280-011-1685-xAuthors
		B. Schultheis, Department of Haematology and Medical Oncology, University of Bochum (Marienhospital Herne), Hoelkeskampring 40, 44625 Herne, GermanyG. Kummer, Department of Haematology and Medical Oncology, University of Bochum (Marienhospital Herne), Hoelkeskampring 40, 4462...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5020066</comments>
            <pubDate>Thu, 07 Jul 2011 05:51:24 +0100</pubDate>
            <guid isPermaLink="false">5020066</guid>        </item>
        <item>
            <title>Matrine induces caspase-dependent apoptosis in human osteosarcoma cells in vitro and in vivo through the upregulation of Bax and Fas/FasL and downregulation of Bcl-2</title>
            <link>http://www.medworm.com/index.php?rid=4993539&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fw1670pq336278023%2F</link>
            <description>Conclusion&amp;nbsp;&amp;nbsp;Our results demonstrate that matrine inhibits the proliferation and induces apoptosis of human osteosarcoma cells in vitro
 and in vivo. The induction of apoptosis appears to occur through the upregulation of Fas/FasL and Bax, downregulation of Bcl-2,
 and activation of caspase-3, -8, and -9, which then trigger major apoptotic cascades.
 
 
 
 
	Content Type Journal ArticlePages 1-15DOI 10.1007/s00280-011-1699-4Authors
		Cheng Zhen Liang, Department of Orthopedics, 2nd Affiliated Hospital, School of Medicine, Zhejiang University, #88 Jie Fang Road, Hangzhou, 310009 Zhejiang, People’s Republic of ChinaJia Kai Zhang, Department of Orthopedics, 2nd Affiliated Hospital, School of Medicine, Zhejiang University, #88 Jie Fang Road, Hangzhou, 310009 Zhejiang, People’s Rep...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4993539</comments>
            <pubDate>Wed, 29 Jun 2011 15:50:40 +0100</pubDate>
            <guid isPermaLink="false">4993539</guid>        </item>
        <item>
            <title>The role of Tau protein in resistance to paclitaxel</title>
            <link>http://www.medworm.com/index.php?rid=4993541&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fm68011x7147r7051%2F</link>
            <description>This article reviews
 current knowledge on predictive value of protein Tau in response to taxanes. Better understanding of its role may facilitate
 patients selection to this sort of treatment and lead to treatment optimization.
 
 
	Content Type Journal ArticlePages 1-5DOI 10.1007/s00280-011-1696-7Authors
		Marta Smoter, Klinika Onkologii Kobiet, Wojskowy Instytut Medyczny, Ul. Szaserów 128, 04-141 Warszawa, PolandLubomir Bodnar, Klinika Onkologii Kobiet, Wojskowy Instytut Medyczny, Ul. Szaserów 128, 04-141 Warszawa, PolandRenata Duchnowska, Klinika Onkologii Kobiet, Wojskowy Instytut Medyczny, Ul. Szaserów 128, 04-141 Warszawa, PolandRafał Stec, Klinika Onkologii Kobiet, Wojskowy Instytut Medyczny, Ul. Szaserów 128, 04-141 Warszawa, PolandBartłomiej Grala, Zakład Patomorfologii, W...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4993541</comments>
            <pubDate>Tue, 28 Jun 2011 15:49:57 +0100</pubDate>
            <guid isPermaLink="false">4993541</guid>        </item>
        <item>
            <title>Triptolide augments the effects of 5-lipoxygenase RNA interference in suppressing pancreatic tumor growth in a xenograft mouse model</title>
            <link>http://www.medworm.com/index.php?rid=4993540&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fe08406t725706716%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;Both treatments exerted antitumor effects in vivo, and combined use of the two approaches produced more powerful antitumor
 effects. Synergistic effects of combined treatment in VEGF expression may contribute to the mechanisms of the strong antitumor
 effects.
 
 
 
 
	Content Type Journal ArticlePages 1-9DOI 10.1007/s00280-011-1698-5Authors
		Xiaoling Ding, Department of Gastroenterology, Affiliated Hospital of Nantong University, 20 Xisi Road, 226001 Nangtong, Jiangsu, People’s Republic of ChinaXiaorong Zhou, Department of Microbiology and Immunology, Medical school of Nantong University, 19 Qixiu Road, 226001 Nantong, Jiangsu, People’s Republic of ChinaHaifeng Zhang, Department of Gastroenterology, Affiliated Hospital of Nantong University, 20 Xisi Road, 22600...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4993540</comments>
            <pubDate>Tue, 28 Jun 2011 15:49:57 +0100</pubDate>
            <guid isPermaLink="false">4993540</guid>        </item>
        <item>
            <title>Oxidative damage to guanine nucleosides following combination chemotherapy with 5-fluorouracil and oxaliplatin</title>
            <link>http://www.medworm.com/index.php?rid=4985519&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F2v46307489710w70%2F</link>
            <description>Conclusion&amp;nbsp;&amp;nbsp;These results indicate that FOLFOX induces ROS in patients and that ROS-generating mechanisms interact.
 
 
 
	Content Type Journal ArticlePages 1-7DOI 10.1007/s00280-011-1700-2Authors
		Shoaib Afzal, Laboratory of Clinical Pharmacology Q7642, Rigshospitalet, 20 Tagensvej, 2200 Copenhagen, DenmarkSøren Astrup Jensen, Department of Oncology, Rigshospitalet, Copenhagen, DenmarkJens Benn Sørensen, Department of Oncology, Rigshospitalet, Copenhagen, DenmarkTrine Henriksen, Laboratory of Clinical Pharmacology Q7642, Rigshospitalet, 20 Tagensvej, 2200 Copenhagen, DenmarkAllan Weimann, Laboratory of Clinical Pharmacology Q7642, Rigshospitalet, 20 Tagensvej, 2200 Copenhagen, DenmarkHenrik Enghusen Poulsen, Laboratory of Clinical Pharmacology Q7642, Rigshospitalet, 20 Tagens...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4985519</comments>
            <pubDate>Mon, 27 Jun 2011 18:11:32 +0100</pubDate>
            <guid isPermaLink="false">4985519</guid>        </item>
        <item>
            <title>Imatinib mesylate in thymic epithelial malignancies</title>
            <link>http://www.medworm.com/index.php?rid=4985518&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fa10254836w553327%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;This trial indicates the lack of effectiveness of imatinib in unselected patients with thymic epithelial tumors. Nevertheless,
 imatinib may represent a valuable option in selected patients with TETs, such as those harboring the V560del c-KIT mutation.
 
 
 
 
	Content Type Journal ArticlePages 1-7DOI 10.1007/s00280-011-1690-0Authors
		Giovannella Palmieri, Molecular and Clinical Endocrinology and Oncology Department, University Federico II, Via Pansini 5, 80128 Naples, ItalyMirella Marino, Department of Pathology, Regina Elena National Cancer Institute, Rome, ItalyCarlo Buonerba, Molecular and Clinical Endocrinology and Oncology Department, University Federico II, Via Pansini 5, 80128 Naples, ItalyPiera Federico, Molecular and Clinical Endocrinology and Oncology Dep...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4985518</comments>
            <pubDate>Mon, 27 Jun 2011 18:11:32 +0100</pubDate>
            <guid isPermaLink="false">4985518</guid>        </item>
        <item>
            <title>The plasma and cerebrospinal fluid pharmacokinetics of the platinum analog satraplatin after intravenous administration in non-human primates</title>
            <link>http://www.medworm.com/index.php?rid=4977347&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fc373x3224l4n6150%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;Satraplatin penetration into CSF is similar to that of carboplatin and cisplatin, despite its greater lipophilicity. The development
 of a phase I trial of satraplatin for refractory childhood solid tumors including brain tumors is in progress.
 
 
 
 
	Content Type Journal ArticlePages 1-6DOI 10.1007/s00280-011-1659-zAuthors
		Leigh Marcus, National Cancer Institute, Pediatric Oncology Branch, 10 Center Drive, Building 10-CRC, Room 1-5742, Bethesda, MD 20892-1101, USARobert Murphy, National Cancer Institute, Pediatric Oncology Branch, 10 Center Drive, Building 10-CRC, Room 1-5742, Bethesda, MD 20892-1101, USAElizabeth Fox, Children’s Hospital of Philadelphia, 3615 Civic Center Blvd, Philadelphia, PA 19104, USACynthia McCully, National Cancer Institute, Pediatric O...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4977347</comments>
            <pubDate>Sat, 25 Jun 2011 15:54:22 +0100</pubDate>
            <guid isPermaLink="false">4977347</guid>        </item>
        <item>
            <title>Effect of ketoconazole-mediated CYP3A4 inhibition on clinical pharmacokinetics of panobinostat (LBH589), an orally active histone deacetylase inhibitor</title>
            <link>http://www.medworm.com/index.php?rid=4977349&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F412q4230377q118l%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;Co-administration of panobinostat with CYP3A inhibitors is feasible as the observed increase in panobinostat PK parameters
 was not considered clinically relevant. Considering the variability in exposure following enzyme inhibition and the fact that
 chronic dosing of panobinostat was not studied with CYP3A inhibitors, close monitoring of panobinostat-related adverse events
 is necessary.
 
 
 
 
	Content Type Journal ArticlePages 1-9DOI 10.1007/s00280-011-1693-xAuthors
		Paul Hamberg, Department of Medical Oncology, Erasmus University Medical Center, Daniel den Hoed Cancer Center, P.O. Box 5201, 3008 AE Rotterdam, The NetherlandsMargaret M. Woo, Novartis Pharmaceutical Corporation, Florham Park, NJ, USALin-Chi Chen, Nevada Cancer Institute, Las Vegas, NV, USAJaap Ve...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4977349</comments>
            <pubDate>Sat, 25 Jun 2011 15:54:21 +0100</pubDate>
            <guid isPermaLink="false">4977349</guid>        </item>
        <item>
            <title>Different combination schedules of gemcitabine with endostar affect antitumor efficacy</title>
            <link>http://www.medworm.com/index.php?rid=4977350&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fh4w5805t7691048w%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;Our finding suggested that endostar given simultaneously with or following gemcitabine might be optimal to enhance the antitumor
 effect.
 
 
 
 
	Content Type Journal ArticlePages 1-8DOI 10.1007/s00280-011-1695-8Authors
		Xing-Chen Peng, Department of Medical Oncology, Cancer Center, The State Key Laboratory of Biotherapy, West China Hospital, West China Medical School, Sichuan University, No. 37, Guo Xue Xiang, Chengdu, 610041 Sichuan Province, ChinaMeng Qiu, Department of Medical Oncology, Cancer Center, The State Key Laboratory of Biotherapy, West China Hospital, West China Medical School, Sichuan University, No. 37, Guo Xue Xiang, Chengdu, 610041 Sichuan Province, ChinaMeng Wei, Department of Medical Oncology, Cancer Center, The State Key Laboratory of Biotherap...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4977350</comments>
            <pubDate>Sat, 25 Jun 2011 05:42:42 +0100</pubDate>
            <guid isPermaLink="false">4977350</guid>        </item>
        <item>
            <title>Pharmacokinetic characterization of a natural product–inspired novel MEK1 inhibitor E6201 in preclinical species</title>
            <link>http://www.medworm.com/index.php?rid=4969912&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Flhk77u9004468616%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;E6201 exhibited high clearance, high to moderate distribution, and fast elimination in preclinical species. In vitro results
 suggested that E6201 has low risk of drug–drug interactions due to CYP inhibition and induction in humans. In the first-in-man
 study, E6201 exhibited high clearance, which was well predicted by allometric scaling.
 
 
 
 
	Content Type Journal ArticlePages 1-9DOI 10.1007/s00280-011-1687-8Authors
		Vipul Kumar, Non-clinical Drug Development, Cubist Pharmaceuticals, 65 Hayden Avenue, Lexington, MA 02421, USAEdgar L. Schuck, DMPK-Andover, Biopharmaceutical Assessments CFU, Eisai Inc., Andover, MA 01810, USARobert D. Pelletier, DMPK-Andover, Biopharmaceutical Assessments CFU, Eisai Inc., Andover, MA 01810, USANadia Farah, DMPK-Andover, Biopharm...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4969912</comments>
            <pubDate>Wed, 22 Jun 2011 16:01:50 +0100</pubDate>
            <guid isPermaLink="false">4969912</guid>        </item>
        <item>
            <title>Phase II study of combined belotecan and cisplatin as first-line chemotherapy in patients with extensive disease of small cell lung cancer</title>
            <link>http://www.medworm.com/index.php?rid=4969913&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fdl23v261505142t4%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;Belotecan and cisplatin combination therapy showed significant efficacy in ED SCLC with improved non-hematologic toxicities.
 
 
 
	Content Type Journal ArticlePages 1-6DOI 10.1007/s00280-011-1689-6Authors
		Junshik Hong, Department of Internal Medicine, Gachon University Gil Hospital, Gachon University of Medicine and Science School of Medicine, 21 Namdongdae-ro 774-gil, Guwol 1-dong, Namdong-gu, Incheon, 405-760 Republic of KoreaMinkyu Jung, Department of Internal Medicine, Gachon University Gil Hospital, Gachon University of Medicine and Science School of Medicine, 21 Namdongdae-ro 774-gil, Guwol 1-dong, Namdong-gu, Incheon, 405-760 Republic of KoreaYu Jin Kim, Department of Internal Medicine, Gachon University Gil Hospital, Gachon University of Medicine and Scien...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4969913</comments>
            <pubDate>Tue, 21 Jun 2011 16:42:40 +0100</pubDate>
            <guid isPermaLink="false">4969913</guid>        </item>
        <item>
            <title>A phase I ascending single-dose study of the safety, tolerability, and pharmacokinetics of bosutinib (SKI-606) in healthy adult subjects</title>
            <link>http://www.medworm.com/index.php?rid=4969914&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fl11xt544611331m5%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;Bosutinib 200–600&amp;nbsp;mg with food was safe and well tolerated. Under fed conditions, bosutinib exposures were linear and dose
 proportional, and C
 max increased by ~1.5-fold. The t
 1/2 supported a once-daily dosing regimen.
 
 
 
 
	Content Type Journal ArticlePages 1-7DOI 10.1007/s00280-011-1688-7Authors
		Richat Abbas, Department of Clinical Pharmacology, Pfizer Inc, 500 Arcola Road, Collegeville, PA 19426, USABruce A. Hug, Department of Clinical Pharmacology, Pfizer Inc, 500 Arcola Road, Collegeville, PA 19426, USACathie Leister, Department of Clinical Pharmacology, Pfizer Inc, 500 Arcola Road, Collegeville, PA 19426, USAMyriam El Gaaloul, Department of Clinical Pharmacology, Pfizer Global Research and Development, Paris, FranceStephan Chalon, Department of ...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4969914</comments>
            <pubDate>Tue, 21 Jun 2011 16:42:39 +0100</pubDate>
            <guid isPermaLink="false">4969914</guid>        </item>
        <item>
            <title>Montelukast attenuates side effects of cisplatin including testicular, spermatological, and hormonal damage in male rats</title>
            <link>http://www.medworm.com/index.php?rid=4946295&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fq509075447460072%2F</link>
            <description>In conclusion, the current study demonstrated that the reproductive
 toxicity caused by CP may be prevented by ML treatment. Thus, it was judged that co-administration of ML with CP may be useful
 to attenuate the negative effects of CP on male reproductive system.
 
 
	Content Type Journal ArticlePages 1-7DOI 10.1007/s00280-011-1692-yAuthors
		Ali Beytur, Faculty of Medicine, Department of Urology, University of Inonu, 44280 Malatya, TurkeyOsman Ciftci, Faculty of Pharmacy, Department of Pharmaceutical Toxicology, University of Inonu, 44280 Malatya, TurkeyFatih Oguz, Faculty of Medicine, Department of Urology, University of Inonu, 44280 Malatya, TurkeyHakan Oguzturk, Faculty Medicine, Department of Emergency Medicine, University of Inonu, 44280 Malatya, TurkeyFethi Yılmaz, Elazig School ...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4946295</comments>
            <pubDate>Fri, 17 Jun 2011 11:58:46 +0100</pubDate>
            <guid isPermaLink="false">4946295</guid>        </item>
        <item>
            <title>Efficacy of increased-dose erlotinib for central nervous system metastases in non-small cell lung cancer patients with epidermal growth factor receptor mutation</title>
            <link>http://www.medworm.com/index.php?rid=4946296&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F0526542223l42733%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;This study indicates that CSF concentrations of erlotinib depend on its plasma concentration. As seen in this patient, high
 CSF concentrations of erlotinib can be achieved by high-dose administration, and this finding suggests the efficacy of high-dose
 administration, especially to refractory CNS metastases of NSCLC patients.
 
 
 
 
	Content Type Journal ArticlePages 1-4DOI 10.1007/s00280-011-1691-zAuthors
		Yosuke Togashi, Department of Respiratory Medicine, Graduate School of Medicine, Kyoto University, 54 Shogoin-Kawaracho, Sakyo-ku, Kyoto, 606-8507 JapanKatsuhiro Masago, Department of Respiratory Medicine, Graduate School of Medicine, Kyoto University, 54 Shogoin-Kawaracho, Sakyo-ku, Kyoto, 606-8507 JapanMasahide Fukudo, Department of Pharmacy, Graduate School...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4946296</comments>
            <pubDate>Fri, 17 Jun 2011 11:58:44 +0100</pubDate>
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        <item>
            <title>5, 7-Dimethoxyflavone sensitizes TRAIL-induced apoptosis through DR5 upregulation in hepatocellular carcinoma cells</title>
            <link>http://www.medworm.com/index.php?rid=4936250&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fa16h962n7243k073%2F</link>
            <description>Conclusion&amp;nbsp;&amp;nbsp;The present study demonstrates that DMF selectively enhances TRAIL-induced apoptosis by ROS-stimulated ER-stress triggering
 CHOP-mediated DR5 upregulation in HCC.
 
 
 
 
	Content Type Journal ArticlePages 1-12DOI 10.1007/s00280-011-1686-9Authors
		Jian-Feng Yang, Medical College, Hunan Normal University, Changsha, 410013 ChinaJian-Guo Cao, Medical College, Hunan Normal University, Changsha, 410013 ChinaLi Tian, Medical College, Hunan Normal University, Changsha, 410013 ChinaFei Liu, Medical College, Hunan Normal University, Changsha, 410013 China
	

	
		Journal Cancer Chemotherapy and PharmacologyOnline ISSN 1432-0843Print ISSN 0344-5704 (Source: Cancer Chemotherapy and Pharmacology)</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4936250</comments>
            <pubDate>Fri, 10 Jun 2011 06:34:30 +0100</pubDate>
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        <item>
            <title>Evaluating rational non-cross-resistant combination therapy in advanced clear cell renal cell carcinoma: combined mTOR and AKT inhibitor therapy</title>
            <link>http://www.medworm.com/index.php?rid=4913233&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fc740552308725155%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;Perifosine is active in select RCC lines, abrogating the induction of AKT phosphorylation mediated by mTOR inhibition. Combined
 mTOR and AKT inhibition resulted in the modulation of pro-angiogenesis pathways, providing a basis for future investigations.
 
 
 
 
	Content Type Journal ArticlePages 1-10DOI 10.1007/s00280-011-1684-yAuthors
		William S. Holland, University of California, Davis Cancer Center, 4501 X Street, Suite, 3016, Sacramento, CA 95817, USAClifford G. Tepper, University of California, Davis Cancer Center, 4501 X Street, Suite, 3016, Sacramento, CA 95817, USAJose E. Pietri, University of California, Davis Cancer Center, 4501 X Street, Suite, 3016, Sacramento, CA 95817, USADanielle C. Chinn, University of California, Davis Cancer Center, 4501 X Street,...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4913233</comments>
            <pubDate>Sun, 05 Jun 2011 05:46:48 +0100</pubDate>
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        <item>
            <title>Preclinical anti-angiogenesis and anti-tumor activity of SIM010603, an oral, multi-targets receptor tyrosine kinases inhibitor</title>
            <link>http://www.medworm.com/index.php?rid=4903692&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fn0nq508846815p65%2F</link>
            <description>Conclusions&amp;nbsp;&amp;nbsp;These results support the clinical assessment of SIM010603 as a therapeutic agent for cancer.
 
 
 
	Content Type Journal ArticlePages 1-11DOI 10.1007/s00280-011-1681-1Authors
		Dongchun Wang, Jiangsu Center for Drug Screening, China Pharmaceutical University, 24 Tong Jia Xiang, Nanjing, 210009 ChinaFeng Tang, Jiangsu Simcere Pharmaceutical R&amp;D Co., Ltd., Nanjing, 210042 ChinaSen Wang, Jiangsu Simcere Pharmaceutical R&amp;D Co., Ltd., Nanjing, 210042 ChinaZhenzhou Jiang, Jiangsu Center for Drug Screening, China Pharmaceutical University, 24 Tong Jia Xiang, Nanjing, 210009 ChinaLuyong Zhang, Jiangsu Center for Drug Screening, China Pharmaceutical University, 24 Tong Jia Xiang, Nanjing, 210009 China
	

	
		Journal Cancer Chemotherapy and PharmacologyOnline ISSN 1432-0843Pr...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4903692</comments>
            <pubDate>Fri, 03 Jun 2011 06:01:11 +0100</pubDate>
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        <item>
            <title>Vascular normalization: a real benefit?</title>
            <link>http://www.medworm.com/index.php?rid=4903693&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fm2x078218k546020%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;It is well established that antibodies to vascular endothelial growth factor (VEGF) in combination with chemotherapeutic agents
 produce synergistic cytotoxicity in a range of cancer. In this review article, it has been analyzed whether the so-called
 vascular normalization of abnormal tumor blood vessels as an effect of VEGF inhibition in association with chemotherapeutic
 agents in the treatment of tumors produces a real benefit. Literature data show that the process of normalization of the structure
 of tumor blood vessels is not always accompanied with a real benefit. In fact as in the case of cerebral tumors, the process
 of normalization may induce a re-establishment of the low permeability characteristics of normal brain microvasculature, preventing
 the delivery...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4903693</comments>
            <pubDate>Fri, 03 Jun 2011 06:01:10 +0100</pubDate>
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        <item>
            <title>A Phase I study to assess the safety, tolerability, and pharmacokinetics of AZD4877, an intravenous Eg5 inhibitor in patients with advanced solid tumors</title>
            <link>http://www.medworm.com/index.php?rid=4903694&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F534271v32m108717%2F</link>
            <description>Conclusion&amp;nbsp;&amp;nbsp;The MTD of AZD4877 given as a 1-h iv infusion on days 1, 8, and 15 of a 28-day cycle was 30&amp;nbsp;mg. At the selected 25&amp;nbsp;mg dose,
 AZD4877 had an acceptable safety profile.
 
 
 
 
	Content Type Journal ArticlePages 1-8DOI 10.1007/s00280-011-1667-zAuthors
		J. R. Infante, Sarah Cannon Research Institute, Nashville, TN, USAR. Kurzrock, The University of Texas M.D. Anderson Cancer Center, 1515 Holcombe Boulevard, Houston, TX 77030, USAJ. Spratlin, University of Colorado Cancer Center, Denver, CO, USAH. A. Burris, Sarah Cannon Research Institute, Nashville, TN, USAS. G. Eckhardt, University of Colorado Cancer Center, Denver, CO, USAJ. Li, AstraZeneca Pharmaceuticals, Wilmington, DE, USAK. Wu, AstraZeneca Pharmaceuticals, Waltham, MA, USAJ. M. Skolnik, AstraZeneca Pha...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4903694</comments>
            <pubDate>Fri, 03 Jun 2011 06:01:09 +0100</pubDate>
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        <item>
            <title>Regulation of chemosensitivity and migration by clusterin in non-small cell lung cancer cells</title>
            <link>http://www.medworm.com/index.php?rid=4903696&amp;cid=s_33439_6_f&amp;fid=33439&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F097378715322077k%2F</link>
            <description>Conclusion&amp;nbsp;&amp;nbsp;Lung cancer cells with high level of CLU have reduced chemosensitivity. High level of CLU may result in migratory inhibition
 and thus favorable prognosis in lung cancer.
 
 
 
 
	Content Type Journal ArticlePages 1-10DOI 10.1007/s00280-011-1682-0Authors
		Ching-Yuan Cheng, Division of General Thoracic Surgery, Department of Surgery, Changhua Christian Hospital, 135 Nanxiao St., Changhua City, Changhua County 500, TaiwanShur-Hueih Cherng, Department of Biotechnology, Hung Kuang University, 34 Chung-Chie Rd, Sha Lu, Taichung City, 443 TaiwanWen-Jun Wu, Institute of Medicine, Chung Shan Medical University, Research Building Room 702, No. 110, Sec. 1, Jianguo N. Road, Taichung City, 402 TaiwanTsung-Ying Yang, Institute of Medicine, Chung Shan Medical University, Research...</description>
            <author>Cancer Chemotherapy and Pharmacology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4903696</comments>
            <pubDate>Wed, 01 Jun 2011 06:00:37 +0100</pubDate>
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