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        <title>Journal of Neuro-Oncology 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 'Journal of Neuro-Oncology' source.</description>
        <link><![CDATA[http://www.medworm.com/rss/search.php?qu=Journal+of+Neuro-Oncology&t=Journal+of+Neuro-Oncology&s=Search&f=source]]></link>
        <lastBuildDate>Wed, 08 Feb 2012 08:41:43 +0100</lastBuildDate>
        <item>
            <title>Prospective cohort study of radiotherapy with concomitant and adjuvant temozolomide chemotherapy for glioblastoma patients with no or minimal residual enhancing tumor load after surgery</title>
            <link>http://www.medworm.com/index.php?rid=5666753&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fy3262k2w0ugtj785%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Survival of glioblastoma patients has been linked to the completeness of surgical resection. Available data, however, were
 generated with adjuvant radiotherapy. Data confirming that extensive cytoreduction remains beneficial to patients treated
 with the current standard, concomitant temozolomide radiochemotherapy, are limited. We therefore analyzed the efficacy of
 radiochemotherapy for patients with little or no residual tumor after surgery. In this prospective, non-interventional multicenter
 cohort study, entry criteria were histological diagnosis of glioblastoma, small enhancing or no residual tumor on post-operative
 MRI, and intended temozolomide radiochemotherapy. The primary study objective was progression-free survival; secondary study
 objectives were surviv...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5666753</comments>
            <pubDate>Fri, 03 Feb 2012 17:53:11 +0100</pubDate>
            <guid isPermaLink="false">5666753</guid>        </item>
        <item>
            <title>Stereotactic radiosurgery for central neurocytoma: a quantitative systematic review</title>
            <link>http://www.medworm.com/index.php?rid=5666754&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fe72j6481511u4622%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Central neurocytoma was originally described as a rare benign neuronal tumor. However, progression and local recurrences after
 surgery are well recognized. Stereotactic radiosurgery is another option for treatment of CN. In order to evaluate the efficacy
 of SRS, we performed a quantitative systematic review of the available data on SRS for CN. To identify eligible studies, systematic
 searches for all CNs treated with SRS were conducted in major scientific publication databases. English studies published
 prior to May 2011 were reviewed and summarized with reference to the inclusion and exclusion criteria. Tumor local control
 was analyzed. Heterogeneity and publication bias were assessed, and the summary control rate and 95% confidence interval (CI)
 were calculated ...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5666754</comments>
            <pubDate>Thu, 02 Feb 2012 17:58:52 +0100</pubDate>
            <guid isPermaLink="false">5666754</guid>        </item>
        <item>
            <title>MGMT promoter hypermethylation and its associations with genetic alterations in a series of 350 brain tumors</title>
            <link>http://www.medworm.com/index.php?rid=5647039&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F75027v32117t0m15%2F</link>
            <description>The objective of this study was to retrospectively investigate MGMT promoter hypermethylation status for a series of 350 human brain tumors, including 275 gliomas of different malignancy grade,
 21 glioblastoma multiforme (GBM) cell lines, and 75 non-glial tumors. The analysis was performed by methylation-specific PCR
 and capillary electrophoresis. MGMT expression at the protein level was also evaluated by both immunohistochemistry (IHC)
 and western blotting analysis. Associations of MGMT hypermethylation with IDH1/IDH2 mutations, EGFR amplification, TP53 mutations, and 1p/19q co-deletion, and the prognostic significance of these, were investigated for the gliomas. MGMT promoter hypermethylation was identified in 37.8% of gliomas, but was not present in non-glial tumors, with the excepti...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5647039</comments>
            <pubDate>Fri, 27 Jan 2012 17:56:38 +0100</pubDate>
            <guid isPermaLink="false">5647039</guid>        </item>
        <item>
            <title>Intracranial Masson tumor: case report and literature review</title>
            <link>http://www.medworm.com/index.php?rid=5647040&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fq77834141t045301%2F</link>
            <description>We report a third case of a neonate who presented with the appearance of a metastatic
 brain tumor involving the orbit, sella, and cerebellum that was ultimately proven to be IPEH. A thorough literature review
 of IPEH is presented and we discuss this clinical entity and its management.
 
 
	Content Type Journal ArticleCategory Case ReportPages 1-7DOI 10.1007/s11060-012-0799-2Authors
		Chie-Schin Shih, Section of Pediatric Hematology/Oncology, Department of Pediatrics, Indiana University School of Medicine, 705 Riley Hospital Drive, Room 4340, Indianapolis, IN 46202, USARichard Burgett, Department of Ophthalmology, Indiana University, Indianapolis and Midwest Eye Institute, 200 West 103rd Street, Indianapolis, IN 46290, USAJose Bonnin, Department of Pathology and Laboratory Medicine, India...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5647040</comments>
            <pubDate>Wed, 25 Jan 2012 18:04:09 +0100</pubDate>
            <guid isPermaLink="false">5647040</guid>        </item>
        <item>
            <title>Molecular and genetic profiles of radiographically defined de novo meningiomas</title>
            <link>http://www.medworm.com/index.php?rid=5638070&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fn001363422777q4j%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;With the exception of radiation-induced tumors, benign meningiomas that are known to have developed within a defined time
 period are extremely rare. We have genetically characterized two cases of radiographically defined de novo, sporadic meningiomas—a
 5-cm, left parasagittal tumor in a 61-year-old male and a 2.3-cm, right falx tumor in a 53-year-old female. Neither tumor
 was observed during MRIs performed for unrelated complaints 49 and 28&amp;nbsp;months before surgery, respectively. Both tumors were
 totally resected, and histopathological examination revealed WHO grade I meningiomas. In both cases, the MIB-1 staining indices
 were high for grade I meningioma (5.6% for case 1 and 9.1% for case 2), and abnormal accumulation of p53 were observed by
 immunohistochemist...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5638070</comments>
            <pubDate>Tue, 24 Jan 2012 18:10:08 +0100</pubDate>
            <guid isPermaLink="false">5638070</guid>        </item>
        <item>
            <title>Clinicopathologic and genomic features of gliosarcomas</title>
            <link>http://www.medworm.com/index.php?rid=5638071&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F712760825303q858%2F</link>
            <description>In conclusion, MGMT methylation and IDH1 mutation are rare events in gliosarcomas, and only aggressive and repetitive local control seems to be effective in treatment
 of gliosarcoma.
 
 
	Content Type Journal ArticleCategory Clinical StudyPages 1-8DOI 10.1007/s11060-011-0790-3Authors
		Dakeun Lee, Department of Pathology, Kyungpook National University Hospital, Kyungpook National University School of Medicine, Daegu, KoreaSo Young Kang, Department of Pathology, Samsung Medical Center, Sungkyunkwan University School of Medicine, 50 Irwon-dong, Gangnam-gu, Seoul, 135-710 Republic of KoreaYeon-Lim Suh, Department of Pathology, Samsung Medical Center, Sungkyunkwan University School of Medicine, 50 Irwon-dong, Gangnam-gu, Seoul, 135-710 Republic of KoreaJi Yun Jeong, Department of Pathology, S...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5638071</comments>
            <pubDate>Tue, 24 Jan 2012 07:32:32 +0100</pubDate>
            <guid isPermaLink="false">5638071</guid>        </item>
        <item>
            <title>P53-dependent antiproliferative and pro-apoptotic effects of trichostatin A (TSA) in glioblastoma cells</title>
            <link>http://www.medworm.com/index.php?rid=5638073&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F67331515q0075115%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Glioblastomas are known to be highly chemoresistant, but HDAC inhibitors (HDACi) have been shown to be of therapeutic relevance
 for this aggressive tumor type. We treated U87 glioblastoma cells with trichostatin A (TSA) to define potential epigenetic
 targets for HDACi-mediated antitumor effects. Using a cDNA array analysis covering 96 cell cycle genes, cyclin-dependent kinase
 inhibitor p21WAF1 was identified as the major player in TSA-induced cell cycle arrest. TSA slightly inhibited proliferation and viability of
 U87 cells, cumulating in a G1/S cell cycle arrest. This effect was accompanied by a significant up-regulation of p53 and its
 transcriptional target p21WAF1 and by down-regulation of key G1/S regulators, such as cdk4, cdk6, and cyclin D1. Nevertheless, TSA...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5638073</comments>
            <pubDate>Tue, 24 Jan 2012 07:32:31 +0100</pubDate>
            <guid isPermaLink="false">5638073</guid>        </item>
        <item>
            <title>Recent advances in the molecular understanding of glioblastoma</title>
            <link>http://www.medworm.com/index.php?rid=5638072&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fe5005w3j17308067%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Glioblastoma is the most common and most aggressive primary brain tumor. Despite maximum treatment, patients only have a median
 survival time of 15&amp;nbsp;months, because of the tumor’s resistance to current therapeutic approaches. Thus far, methylation of
 the O
 6-methylguanine-DNA methyltransferase (MGMT) promoter has been the only confirmed molecular predictive factor in glioblastoma.
 Novel “genome-wide” techniques have identified additional important molecular alterations as mutations in isocitrate dehydrogenase
 1 (IDH1) and its prognostic importance. This review summarizes findings and techniques of genetic, epigenetic, transcriptional, and
 proteomic studies of glioblastoma. It provides the clinician with an up-to-date overview of current identified molecu...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5638072</comments>
            <pubDate>Tue, 24 Jan 2012 07:32:31 +0100</pubDate>
            <guid isPermaLink="false">5638072</guid>        </item>
        <item>
            <title>Lexical access speed is significantly correlated with the return to professional activities after awake surgery for low-grade gliomas</title>
            <link>http://www.medworm.com/index.php?rid=5638074&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fm07213372v2rtg02%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Awake surgery with intraoperative brain mapping is highly recommended for patients with diffuse low-grade gliomas in language
 areas, to maximise the extent of resection while preserving the integrity of functional networks and thus quality of life.
 The picture-naming test “DO.80” is the gold standard for language assessment before, during, and after surgery. Cognitive
 functioning is correlated with quality of life, itself linked with return to work. Our objective was to evaluate the significance
 of measuring naming speed, and its correlation with the return to professional activities. Two complementary studies are reported.
 In the first retrospective study, eleven patients were examined post-operatively. Five patients were selected because they
 were not able t...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5638074</comments>
            <pubDate>Tue, 24 Jan 2012 07:32:29 +0100</pubDate>
            <guid isPermaLink="false">5638074</guid>        </item>
        <item>
            <title>Initial experience with bendamustine in patients with recurrent primary central nervous system lymphoma: a case report</title>
            <link>http://www.medworm.com/index.php?rid=5619678&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fln47g4700802k187%2F</link>
            <description>This report describes the first known experience of patients with RPCNSL treated with bendamustine. Therapy was well-tolerated
 and best response was noted as stable disease after eight cycles of bendamustine followed by a subsequent local systemic recurrence
 found at five months follow-up. CNS involvement in this patient remained stable 20&amp;nbsp;+&amp;nbsp;months post-bendamustine treatment. Based
 on our observations, further neuropharmacokinetic and efficacy studies with bendamustine may be warranted in this patient
 population.
 
 
	Content Type Journal ArticleCategory Case ReportPages 1-5DOI 10.1007/s11060-011-0788-xAuthors
		Jaclyn J. Renfrow, Wake Forest School of Medicine, Winston-Salem, NC 27157, USAAlisha DeTroye, Department of Internal Medicine, Section on Hematology and Oncology, C...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5619678</comments>
            <pubDate>Tue, 17 Jan 2012 07:19:32 +0100</pubDate>
            <guid isPermaLink="false">5619678</guid>        </item>
        <item>
            <title>Physiological 18F-FDG uptake by the spinal cord: is it a point of consideration for cancer patients?</title>
            <link>http://www.medworm.com/index.php?rid=5619677&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fv7263225041m7025%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;It is essential to be familiar with normal patterns of 18F FDG distribution in the whole body for accurate PET interpretation. We assessed FDG uptake by the spinal cord to evaluate
 its characteristics in cancer patients. For 101 cancer patients who underwent 18F FDG PET/CT the spinal cord along its segments was visually assessed for FDG uptake, regarding MaxSUV-measurement ≥1 as cut-off
 point. This assessment was correlated with the patient’s database variables. MRI and FDG PET-CT follow-up were included in
 the evaluation of positive subjects with FDG cord uptake. Forty-nine (48.5%) were positive for FDG cord uptake. The most encountered
 sites were the eleventh and twelfth dorsal vertebrae (36/49; 73.5%), all cervical (24/49; 49%), and the first lumbar segments
...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5619677</comments>
            <pubDate>Tue, 17 Jan 2012 07:19:32 +0100</pubDate>
            <guid isPermaLink="false">5619677</guid>        </item>
        <item>
            <title>Induction of cell-cycle arrest and apoptosis in glioblastoma stem-like cells by WP1193, a novel small molecule inhibitor of the JAK2/STAT3 pathway</title>
            <link>http://www.medworm.com/index.php?rid=5619676&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fd41746283777544l%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Glioma stem-like cells (GSCs) may be the initiating cells in glioblastoma (GBM) and contribute to the resistance of these
 tumors to conventional therapies. Development of novel chemotherapeutic agents and treatment approaches against GBM, especially
 those specifically targeting GSCs are thus necessary. In the present study, we found that a novel Janus kinase 2/Signal Transducer
 and Activator of Transcription 3 (JAK2/STAT3) pathway inhibitor (WP1193) significantly decreased the proliferation of established
 glioma cell lines in vitro and inhibit the growth of glioma in vivo. To test the efficacy of WP1193 against GSCs, we then
 administrated WP1193 to GSCs isolated and expanded from multiple human GBM tumors. We revealed that WP1193 suppressed phosphorylation
 of JAK2...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5619676</comments>
            <pubDate>Tue, 17 Jan 2012 07:19:32 +0100</pubDate>
            <guid isPermaLink="false">5619676</guid>        </item>
        <item>
            <title>Risk of ischemia in glioma surgery: comparison of first and repeat procedures</title>
            <link>http://www.medworm.com/index.php?rid=5619679&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fu24j2p6v5t9n2743%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The role of repeat resection in the multimodal treatment of gliomas is unclear. Repeat surgery theoretically carries a higher
 risk of inducing neurological deficits, which might even out any advantage of cytoreduction. We sought to determine whether
 the occurrence of perioperative infarction is higher for repeat surgery than for first surgery, and sought to identify factors
 associated with the occurrence of postoperative infarction. Therefore, we searched our database to identify patients who were
 operated for primary or recurrent glial tumors between October 2007 and October 2010. We analyzed 177 procedures, of which
 130 (73.4%) were first surgeries and 47 (26.5%) were repeat. Initial WHO grades, KPS scores, and age were evenly distributed
 between the groups. For...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5619679</comments>
            <pubDate>Tue, 17 Jan 2012 07:19:31 +0100</pubDate>
            <guid isPermaLink="false">5619679</guid>        </item>
        <item>
            <title>Targeting Aurora Kinase A enhances radiation sensitivity of atypical teratoid rhabdoid tumor cells</title>
            <link>http://www.medworm.com/index.php?rid=5608146&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fmw08ku69544kj647%2F</link>
            <description>The objective of this study was to evaluate the impact of Aurora Kinase A inhibition in ATRT cell lines.
 Our analysis revealed that inhibition of Aurora Kinase A induces cell death in ATRT cells and the small molecule inhibitor
 MLN 8237 sensitizes these cells to radiation. Furthermore, inhibition of Aurora Kinase A resulted in decreased activity of
 pro-proliferative signaling pathways. These data indicate that inhibition of Aurora Kinase A is a promising small molecule
 target for ATRT therapy.
 
 
	Content Type Journal ArticleCategory Laboratory InvestigationPages 1-10DOI 10.1007/s11060-011-0795-yAuthors
		Sujatha Venkataraman, Department of Pediatrics, Children’s Hospital Colorado, University of Colorado School of Medicine, Anschutz Medical Campus, Aurora, CO, USAIrina Alimova, Depa...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5608146</comments>
            <pubDate>Sat, 14 Jan 2012 16:41:36 +0100</pubDate>
            <guid isPermaLink="false">5608146</guid>        </item>
        <item>
            <title>Stereotactic radiosurgery for primary and metastatic sarcomas involving the spine</title>
            <link>http://www.medworm.com/index.php?rid=5608147&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fv60v657284882w16%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The treatment for spinal sarcomas is difficult due to inadequate surgical margin and an inability to deliver high dose radiation.
 Advanced technology of stereotactic radiosurgery (SRS) enabled higher biological effective doses of radiation to be delivered
 to spinal sarcomas by hypofractionation method. The authors evaluated local control rate following SRS for primary and metastatic
 spinal sarcomas. Thirty-two spinal sarcomas (10 primary tumors, 22 metastatic tumors) in 27 patients were treated by SRS from
 November 2002 to September 2009. Patients were assessed for pain status, neurological status and radiological response by
 regular follow-up. Overall survival and local progression-free survival were calculated and prognostic factors were sought.
 Median tumor vol...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5608147</comments>
            <pubDate>Sat, 14 Jan 2012 16:41:35 +0100</pubDate>
            <guid isPermaLink="false">5608147</guid>        </item>
        <item>
            <title>Spurious progression in pediatric brain tumors</title>
            <link>http://www.medworm.com/index.php?rid=5596933&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fxn52712187434h85%2F</link>
            <description>In this study, we sought to characterize post-therapy MRI changes mimicking progression, which we refer to as “spurious progression”
 (SP) in children with brain tumors. We analyzed whether SP is associated with particular tumor types or therapeutic modalities.
 Between 2000 and 2009, we identified 181 consecutive children &amp;lt;21&amp;nbsp;years of age at our center who were treated for brain tumors
 and had at least three MRI scans within a year after completing therapy. SP was defined as MRI abnormalities characterized
 by increase in size, enhancement, edema, or cystic changes within 12&amp;nbsp;months following therapy, and stabilization or improvement
 on subsequent imaging. One-hundred forty-one patients with brain tumors were evaluable. Fifty-six (40%) had imaging abnormalities
 initiall...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5596933</comments>
            <pubDate>Thu, 12 Jan 2012 06:42:15 +0100</pubDate>
            <guid isPermaLink="false">5596933</guid>        </item>
        <item>
            <title>Characterization and outcomes of optic nerve gliomas: a population-based analysis</title>
            <link>http://www.medworm.com/index.php?rid=5596934&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fw351p04j5mp18303%2F</link>
            <description>In conclusion, ONG are rare tumors seen predominantly in children. The overall prognosis of high-grade
 tumors remains poor in all age groups despite multi-modality treatment.
 
 
	Content Type Journal ArticleCategory Clinical StudyPages 1-7DOI 10.1007/s11060-011-0783-2Authors
		Mark V. Mishra, Department of Radiation Oncology, Jefferson Medical College, Philadelphia, PA, USADavid W. Andrews, Department of Neurosurgery, Jefferson Medical College, Philadelphia, PA, USAJon Glass, Department of Neurosurgery, Jefferson Medical College, Philadelphia, PA, USAJames J. Evans, Department of Neurosurgery, Jefferson Medical College, Philadelphia, PA, USAAdam P. Dicker, Department of Radiation Oncology, Jefferson Medical College, Philadelphia, PA, USAXinglei Shen, Department of Radiation Oncology, Jef...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5596934</comments>
            <pubDate>Thu, 12 Jan 2012 06:42:14 +0100</pubDate>
            <guid isPermaLink="false">5596934</guid>        </item>
        <item>
            <title>An experimental xenograft mouse model of diffuse pontine glioma designed for therapeutic testing</title>
            <link>http://www.medworm.com/index.php?rid=5596935&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fl6884m1064lm46x0%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The prognosis for diffuse infiltrating pontine gliomas (DIPG) remains extremely poor, with the majority of patients surviving
 less than 2&amp;nbsp;years. Here, we have adapted standard xenograft techniques to study glioma growth in the mouse brainstem, and
 have utilized the mouse model for studying a relevant therapeutic for treating DIPGs. bioluminescence imaging monitoring revealed
 a progressive increase in signal following the injection of either of two tumor cell types into the brainstem. Mice with orthotopic
 GS2 tumors, and receiving a single 100&amp;nbsp;mg/kg dose of temozolomide showed a lengthy period of decreased tumor luminescence,
 with substantially increased survival relative to untreated mice (P&amp;nbsp;&amp;lt;&amp;nbsp;0.001). A small molecule inhibitor that targets c...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5596935</comments>
            <pubDate>Mon, 09 Jan 2012 19:34:42 +0100</pubDate>
            <guid isPermaLink="false">5596935</guid>        </item>
        <item>
            <title>Contribution of CSF cytology in the diagnostic work-up of breast cancer patients with neurological symptoms: a retrospective analysis over two decades</title>
            <link>http://www.medworm.com/index.php?rid=5571953&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F93741l40814385l2%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The aim of this study was to evaluate the contribution of cytological analysis of cerebrospinal fluid (CSF) in the diagnostic
 work-up of breast cancer patients who present with neurological symptoms suspected for central nervous system (CNS) metastases.
 In the period 1989–2009, a total of 81 patients with breast cancer underwent CSF cytological examination. Relevant tumour
 characteristics, clinical presentation and radiological findings were scored. The CSF cytological diagnosis was classified
 according to the 1996 NCI-sponsored conference approach as malignant, suspicious for malignancy, atypical, benign or inadequate.
 During the course of 20&amp;nbsp;years, 145 CSF cytological examinations were performed. Relatively common neurological symptoms resulting
 in cytolo...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5571953</comments>
            <pubDate>Wed, 04 Jan 2012 06:58:45 +0100</pubDate>
            <guid isPermaLink="false">5571953</guid>        </item>
        <item>
            <title>Outcomes after discontinuation of antiepileptic drugs after surgery in patients with low grade brain tumors and meningiomas</title>
            <link>http://www.medworm.com/index.php?rid=5571954&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F33345570584g6p34%2F</link>
            <description>We examined patients with
 low grade supratentorial brain tumors to determine characteristics of patients who underwent AED withdrawal. A retrospective
 chart review was performed in patients who underwent resection between 1/1/2004 and 12/31/2005 at a single center. Data were
 collected regarding the use of postoperative AEDs, occurrence of postoperative seizures, and patient/tumor characteristics.
 We examined 169 patients with a median follow-up of 3.1&amp;nbsp;years. AEDs were withdrawn or never started in 111 patients; post-withdrawal
 seizures occurred in 11 (9.9%). The rate was similar between meningiomas and primary brain tumors. No independent risk factors
 for post-withdrawal seizures were found. Of 58 patients whose AEDs were not withdrawn, postoperative seizures occurred in
 28 (48...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5571954</comments>
            <pubDate>Mon, 02 Jan 2012 16:53:20 +0100</pubDate>
            <guid isPermaLink="false">5571954</guid>        </item>
        <item>
            <title>Bevacizumab for glioblastoma refractory to vascular endothelial growth factor receptor inhibitors</title>
            <link>http://www.medworm.com/index.php?rid=5552023&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F84n881368622m813%2F</link>
            <description>We report our experience with bevacizumab
 (BEV), a VEGF targeting antibody, following failure of a VEGF receptor targeting tyrosine kinase inhibitor (TKI). We retrospectively
 identified patients treated on clinical trials with VEGFR–TKIs for recurrent GBM followed by BEV at next recurrence. Survival
 was estimated by the Kaplan–Meier method. Fourteen patients were identified (six women; median age 57). All received VEGFR–TKIs
 (sunitinib 11, cediranib 2, sorafenib 1) then BEV at next recurrence. There were no radiographic responses to VEGFR–TKIs;
 best response was stable disease in 50% (7/14). Patients received BEV alone (21%, 3/14) or in combination with chemotherapy
 (79%, 11/14). On BEV, 29% (4/14) had a partial response, and 36% (5/14) stabilized. Of evaluable patients, 42% ...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5552023</comments>
            <pubDate>Wed, 28 Dec 2011 06:53:39 +0100</pubDate>
            <guid isPermaLink="false">5552023</guid>        </item>
        <item>
            <title>Secondary intramedullary spinal cord non-Hodgkin’s lymphoma</title>
            <link>http://www.medworm.com/index.php?rid=5544156&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fvk322q4978753501%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Intramedullary spinal cord metastases of solid neoplasms are associated with poor long-term survival. As the characteristics
 of secondary intramedullary spinal cord non-Hodgkin’s lymphoma (NHL) are not well understood, we sought to describe its clinical
 features and outcome. We retrospectively reviewed the Mayo Clinic patient database, lymphoma database, and pathology records
 from 1996 to 2010 and identified patients with clinical myelopathy and neuroimaging evidence of secondary intramedullary spinal
 cord involvement from pathologically confirmed systemic NHL. Seven patients were included in this study. The median age was
 61&amp;nbsp;years (range, 41–81). Symptom onset was subacute (≤8&amp;nbsp;weeks) in six. Four patients were wheelchair-dependent at diagnosis.
 Sp...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5544156</comments>
            <pubDate>Thu, 22 Dec 2011 06:44:04 +0100</pubDate>
            <guid isPermaLink="false">5544156</guid>        </item>
        <item>
            <title>Expression of RECK in endothelial cells of glioma: comparison with CD34 and VEGF expressions</title>
            <link>http://www.medworm.com/index.php?rid=5537460&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Far25p6576h44v81t%2F</link>
            <description>In this study, we aimed to determine whether high
 micro-vessel density (MVD) expressed by RECK in glioma tissue is correlated with grades of glioma. We also compared RECK expression
 with that of the formerly known vessel marker, CD34, and vascular endothelial growth factor (VEGF). RECK, CD34, and VEGF immuno-reactivities
 of 72 glioma tissues were studied. RECK was seen in microvessels of glioma tissues. CD34 showed a similar pattern to RECK,
 whereas VEGF showed positive staining in cytoplasm of tumor cells and endothelial cells. Average MVD with RECK was 107.6 microvessels
 (range 7–290). RECK was positively correlated with grades of glioma. RECK and CD34 also showed a strong correlation (P&amp;nbsp;=&amp;nbsp;0.001). Higher frequency of VEGF staining was also correlated with higher grade of...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5537460</comments>
            <pubDate>Tue, 20 Dec 2011 06:47:31 +0100</pubDate>
            <guid isPermaLink="false">5537460</guid>        </item>
        <item>
            <title>Use of recombinant tissue plasminogen activator in cancer patients with acute stroke</title>
            <link>http://www.medworm.com/index.php?rid=5524120&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Frh27gw81w0122864%2F</link>
            <description>We report six patients
 with cancer treated with rTPA at our institution, four of whom had early neurologic recovery. Only one of our six patients
 suffered minor bleeding as a complication of rTPA. Acute stroke in patients with cancer may be treated with rTPA, and active
 cancer should not be considered an absolute contraindication to rTPA use.
 
 
	Content Type Journal ArticleCategory Clinical Study - Patient StudyPages 1-3DOI 10.1007/s11060-011-0780-5Authors
		Jerome J. Graber, Department of Neurology, Memorial Sloan-Kettering Cancer Center, 1275 York Avenue, New York, NY 10065, USALakshmi Nayak, Department of Neurology, Memorial Sloan-Kettering Cancer Center, 1275 York Avenue, New York, NY 10065, USALisa M. DeAngelis, Department of Neurology, Memorial Sloan-Kettering Cancer Center, 127...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5524120</comments>
            <pubDate>Sat, 17 Dec 2011 16:43:39 +0100</pubDate>
            <guid isPermaLink="false">5524120</guid>        </item>
        <item>
            <title>Medulloblasoma: challenges for effective immunotherapy</title>
            <link>http://www.medworm.com/index.php?rid=5515046&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F1648603865504775%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;For medulloblastoma patients, the current therapeutic paradigm of surgery followed by radiation and chemotherapy can lead
 to long-term remission. However, the sequelae of treatment can be very debilitating, particularly in young children. Immunotherapy
 is an attractive treatment approach to optimize the targeting of tumor cells while sparing the vulnerable surrounding brain
 that is still developing in children. Understanding the relationship between medulloblastoma and the immune system is critical
 to develop effective immunologic-based treatment strategies for these patients. This review focuses on current knowledge of
 tumor immunology and the factors that contribute to the lack of immune system recognition of these tumors. The specificity
 of tumor antigens prese...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5515046</comments>
            <pubDate>Thu, 15 Dec 2011 16:51:12 +0100</pubDate>
            <guid isPermaLink="false">5515046</guid>        </item>
        <item>
            <title>Independent prognostic value of pre-treatment 18-FDG-PET in high-grade gliomas</title>
            <link>http://www.medworm.com/index.php?rid=5515047&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F617614358506j477%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The prognostic value of PET with (18F)-fluoro-2-deoxy-d-glucose (FDG) has been shown in high-grade gliomas (HGG), but not compared with consensual prognostic factors. We sought
 to evaluate the independent predictive value of pre-treatment FDG-PET on overall (OS) and event-free survival (EFS). We retrospectively
 analyzed 41 patients with histologically-confirmed HGG (31 glioblastomas and 10 anaplastic gliomas). The pre-treatment uptake
 of FDG was assessed qualitatively by five-step visual metabolic grading, and quantitatively by the ratio between the tumor
 and contralateral maximal standardized uptake value (T/CL). EFS and OS following PET were compared with FDG uptake by univariate
 analysis, and by two multivariate analyses: one including main consensual prognostic...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5515047</comments>
            <pubDate>Thu, 15 Dec 2011 06:43:55 +0100</pubDate>
            <guid isPermaLink="false">5515047</guid>        </item>
        <item>
            <title>F10 gene hypomethylation, a putative biomarker for glioma prognosis</title>
            <link>http://www.medworm.com/index.php?rid=5515048&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F3324j7u476175754%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Tumors are usually characterized by an imbalance in cytosine methylation, including hypomethylation of CpG islands. In this
 study, bisulfite sequencing PCR was used to assess the promoter methylation status of coagulation factor X (F10) gene in tumors
 of 96 glioma patients and in glioma cells U251, SF767, and SF126, and the effect of promoter hypomethylation on protein expression
 was evaluated immunohistochemically. The study showed that the demethylation ratio of F10 in SF126, SF767, and U251 cells
 was 38.6, 26.4, and 24.3% respectively. Hypomethylation of F10 was detected in 82.3% of glioma specimens and in no normal
 brain tissues, with significant correlation with its protein expression. However there was no remarkable relationship between
 F10 hypomethylation a...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5515048</comments>
            <pubDate>Tue, 13 Dec 2011 06:57:24 +0100</pubDate>
            <guid isPermaLink="false">5515048</guid>        </item>
        <item>
            <title>β-Elemene inhibits Hsp90/Raf-1 molecular complex inducing apoptosis of glioblastoma cells</title>
            <link>http://www.medworm.com/index.php?rid=5504338&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F0j246lr84151j832%2F</link>
            <description>In this study, we report that β-elemene
 disrupted the formation of the Hsp90/Raf-1 complex, a key step in maintaining the conformation stability of Raf-1, and caused
 deactivation of Raf-1 and inhibition of the ERK pathway, thereby leading to apoptosis of glioblastoma cells. Specifically,
 treatment of glioblastoma cell lines with β-elemene attenuated phosphorylation of multiple members of the kinase families
 in the Ras/Raf/MEK/ERK cascade, including Raf-1 and ERK as well as downstream signaling targets such as Bcl-2. These results
 suggest that the Hsp90/Raf-1 complex could be a promising molecular target for new drug development for the treatment of glioblastoma.
 
 
	Content Type Journal ArticleCategory Laboratory Investigation - Human/Animal TissuePages 1-8DOI 10.1007/s11060-011-07...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5504338</comments>
            <pubDate>Sun, 11 Dec 2011 06:33:35 +0100</pubDate>
            <guid isPermaLink="false">5504338</guid>        </item>
        <item>
            <title>Unrecognized visual field deficits in children with primary central nervous system brain tumors</title>
            <link>http://www.medworm.com/index.php?rid=5476152&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F2507q0183q28g875%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Visual field deficits can be a consequence of brain tumor location or treatment. The prevalence of unrecognized visual field
 deficits in children diagnosed with brain tumors is not known. All children at a single tertiary care pediatric children’s
 hospital diagnosed with a primary brain tumor were tested for visual field deficits by a child neurologist and neuro-ophthalmologist
 over 16&amp;nbsp;months. Children with reproducible visual field deficits on two separate occasions were included in the analysis.
 Patients with optic glioma, craniopharyngioma, or previously known visual field deficits were excluded. Fourteen of 92 (15.2%)
 children (average 8.9&amp;nbsp;years, 8 girls) had undiagnosed visual field deficits. Average time between diagnosis of tumor and unrecognized...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5476152</comments>
            <pubDate>Sat, 03 Dec 2011 16:50:40 +0100</pubDate>
            <guid isPermaLink="false">5476152</guid>        </item>
        <item>
            <title>Atypical teratoid/rhabdoid tumors: the need for more active therapeutic measures in younger patients</title>
            <link>http://www.medworm.com/index.php?rid=5476153&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fx028h8046t055225%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Despite active and aggressive therapeutic measures, atypical teratoid/rhabdoid tumors (AT/RTs) are without doubt one of the
 most malignant brain tumors that occur during childhood. These tumors are more prevalent in children less than 3&amp;nbsp;years of
 age, and the prognosis is worse in these young children. Medical records of 14 patients diagnosed at our institution were
 reviewed. Patients diagnosed with AT/RT at our institution between 1997 and 2009 were identified. Clinical data for those
 patients with pathologic confirmation of AT/RTs were reviewed regarding surgery, adjuvant treatment, and survival. A total
 of 14 patients were identified. One patient who died 3&amp;nbsp;days after initial surgery was excluded, and 13 patients were recruited.
 Of the 13 patients, 7 w...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5476153</comments>
            <pubDate>Fri, 02 Dec 2011 06:47:36 +0100</pubDate>
            <guid isPermaLink="false">5476153</guid>        </item>
        <item>
            <title>Hydroxyurea for recurrent surgery and radiation refractory high-grade meningioma</title>
            <link>http://www.medworm.com/index.php?rid=5468407&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fn83q2504w4074874%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Hydroxyurea (HU), an orally administered chemotherapy, has become the de facto standard chemotherapeutic agent in patients with surgically and radiation refractory meningiomas based on a limited literature.
 A retrospective case series of 35 patients with recurrent WHO Grade 2 (n&amp;nbsp;=&amp;nbsp;22) or 3 (n&amp;nbsp;=&amp;nbsp;13) meningioma treated with HU following progression after surgery and radiotherapy was collated with primary study objectives
 of overall response rate, median and progression free survival (PFS) at 6-months. Thirty-five patients (25 women; 10 men:
 median age 63&amp;nbsp;years, range 34–86) with recurrent high-grade meningioma were treated with HU (1,000&amp;nbsp;mg/m2 orally divided twice per day; one cycle operationally defined as 4&amp;nbsp;weeks of daily HU). Pat...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5468407</comments>
            <pubDate>Wed, 30 Nov 2011 04:54:49 +0100</pubDate>
            <guid isPermaLink="false">5468407</guid>        </item>
        <item>
            <title>Early rehabilitation after surgery improves functional outcome in inpatients with brain tumours</title>
            <link>http://www.medworm.com/index.php?rid=5456979&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F40646213172r12pu%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Clinical experience suggests that application of the fundamental principles of rehabilitation medicine can improve the care
 of patients with cancer. Despite the high incidence of neurological and functional deficits in patients affected by brain
 tumours (BTs), rehabilitation treatment of this population is not as well established as it is for patients with other neurological
 conditions. To assess functional outcome in brain tumour inpatients who underwent early rehabilitation after surgery. 75 patients
 who had undergone neurosurgery for primary BTs and 75 patients affected by stroke were enrolled in a case-control study. All
 patients were evaluated by means of a core set of clinical scales (Functional Independence Measure, Sitting Balance score,
 Standing Balance s...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5456979</comments>
            <pubDate>Mon, 28 Nov 2011 16:50:13 +0100</pubDate>
            <guid isPermaLink="false">5456979</guid>        </item>
        <item>
            <title>Novel cell lines established from pediatric brain tumors</title>
            <link>http://www.medworm.com/index.php?rid=5456980&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fb36365x213352101%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The paucity of cell culture models for childhood brain tumors prompted us to establish pediatric cell lines for use in biological
 experiments and preclinical developmental therapeutic studies. Three cell lines were established, CHLA-200 (GBM), CHLA-259
 (anaplastic medulloblastoma) and CHLA-266 (atypical teratoid rhabdoid tumor, AT/RT). Consistent with an AT/RT origin, CHLA-266
 lacked INI1 expression and had monosomy 22. All lines had unique DNA short tandem repeat “fingerprints” matching that of the
 patient’s tumor tissue and were adherent on tissue culture plastic, but differed in morphology and doubling times. CHLA-200
 had a silent mutation in TP53. CHLA-259 and CHLA-266 had wild-type TP53. All three lines were relatively resistant to multiple drugs when co...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5456980</comments>
            <pubDate>Sat, 26 Nov 2011 16:48:04 +0100</pubDate>
            <guid isPermaLink="false">5456980</guid>        </item>
        <item>
            <title>Erratum to: Sporadic CNS hemangioblastomatosis, response to sunitinib and secondary polycythemia</title>
            <link>http://www.medworm.com/index.php?rid=5449521&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fv595816217085462%2F</link>
            <description>Content Type Journal ArticleCategory ErratumPages 1-1DOI 10.1007/s11060-011-0773-4Authors
		German Reyes-Botero, AP-HP, Groupe Hospitalier Pitié-Salpêtrière, Service de Neurologie Mazarin, Hôpital de la Salpêtrière, 47 Bd de l’Hôpital, 75013 Paris, FranceJaime Gállego Pérez-Larraya, AP-HP, Groupe Hospitalier Pitié-Salpêtrière, Service de Neurologie Mazarin, Hôpital de la Salpêtrière, 47 Bd de l’Hôpital, 75013 Paris, FranceMarc Sanson, AP-HP, Groupe Hospitalier Pitié-Salpêtrière, Service de Neurologie Mazarin, Hôpital de la Salpêtrière, 47 Bd de l’Hôpital, 75013 Paris, France
	

	
		Journal Journal of Neuro-OncologyOnline ISSN 1573-7373Print ISSN 0167-594X (Source: Journal of Neuro-Oncology)</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5449521</comments>
            <pubDate>Fri, 25 Nov 2011 17:56:56 +0100</pubDate>
            <guid isPermaLink="false">5449521</guid>        </item>
        <item>
            <title>Treatment of chordoma with imatinib complicated by intracranial hemorrhage: a case showing dissociation between biological effect and therapeutic outcome</title>
            <link>http://www.medworm.com/index.php?rid=5449520&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F53400jh10q497331%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorPages 1-3DOI 10.1007/s11060-011-0767-2Authors
		François Mercier, Massachusetts General Hospital, 185 Cambridge Street, Boston, MA 02114, USAMarie-Christine Guiot, Montreal Neurological Institute, Montreal, CanadaMichel W. Bojanowski, Centre Hospitalier de l’Universite de Montreal, Montreal, Canada
	

	
		Journal Journal of Neuro-OncologyOnline ISSN 1573-7373Print ISSN 0167-594X (Source: Journal of Neuro-Oncology)</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5449520</comments>
            <pubDate>Fri, 25 Nov 2011 17:56:56 +0100</pubDate>
            <guid isPermaLink="false">5449520</guid>        </item>
        <item>
            <title>Targeting DNA repair and the cell cycle in glioblastoma</title>
            <link>http://www.medworm.com/index.php?rid=5449522&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fy511443467152u7l%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Glioblastoma is a disease with poor outcomes despite standard therapy. Specific targeting of the DNA damage response is a
 strategy that is becoming increasingly employed in oncology and has intriguing potential for improving outcomes in glioblastoma.
 DNA damage targeting has implications for improving current therapy as well as the potential to leverage inherent differences
 in glioblastoma cells to widen the therapeutic window.
 
 
	Content Type Journal ArticleCategory Topic ReviewPages 1-15DOI 10.1007/s11060-011-0765-4Authors
		Brian M. Alexander, Department of Radiation Oncology, Dana-Farber/Brigham and Women’s Cancer Center, Harvard Medical School, 75 Francis Street, ASB1-L2, Boston, MA 02115, USANancy Pinnell, Department of Radiation Oncology, Dana-Farber/Brigh...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5449522</comments>
            <pubDate>Wed, 23 Nov 2011 17:42:39 +0100</pubDate>
            <guid isPermaLink="false">5449522</guid>        </item>
        <item>
            <title>Chlorotoxin-conjugated nanoparticles as potential glioma-targeted drugs</title>
            <link>http://www.medworm.com/index.php?rid=5449523&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fw62688vl6664vn45%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Development of glioma-specific nanoparticles has been an area of intense research over the past several years. Iron oxide,
 multifunctional superparamagnetic, and NaYF4:Yb,rare-earth upconversion nanoparticles, conjugated with chlorotoxin (CTX, a key toxin in scorpion venom which has been
 shown to bind specifically to glioma cell surface as a specific chloride channel and matrix metalloproteinase-2 blocker),
 exhibit high affinity for glioma and direct tumor visualization. We review the latest improvements of CTX-modified nanoparticle
 platforms which might enable development of more effective therapeutic agents in clinical treatment of glioma.
 
 
	Content Type Journal ArticleCategory Topic ReviewPages 1-6DOI 10.1007/s11060-011-0763-6Authors
		Yuejun Fu, Key Laborator...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5449523</comments>
            <pubDate>Tue, 22 Nov 2011 17:56:32 +0100</pubDate>
            <guid isPermaLink="false">5449523</guid>        </item>
        <item>
            <title>Hypofractionated radiotherapy with or without concurrent temozolomide in elderly patients with glioblastoma multiforme: a review of ten-year single institutional experience</title>
            <link>http://www.medworm.com/index.php?rid=5440338&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fk420176111462531%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The landmark Stupp study demonstrated a survival advantage with concomitant and adjuvant temozolomide (TMZ) with standard
 radiotherapy (RT) in glioblastoma multiforme (GBM) patients but excluded those older than 70&amp;nbsp;years. The prospective Roa study
 of older GBM patients treated with hypofractionated 3-week course RT demonstrated equivalence to standard 6-week course
 RT. Taken together, these trials suggest hypofractionated RT with TMZ may be a reasonable treatment option for elderly GBM
 patients. We conducted a retrospective review of GBM patients (age ≥60&amp;nbsp;years) treated with hypofractionated RT and temozolomide
 at our institution between 2000 and 2010. We identified 112 patients who received hypofractionated RT, with 57 receiving
 concurrent and adjuvan...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5440338</comments>
            <pubDate>Mon, 21 Nov 2011 18:07:25 +0100</pubDate>
            <guid isPermaLink="false">5440338</guid>        </item>
        <item>
            <title>Pilot study on sex hormone levels and fertility in women with malignant gliomas</title>
            <link>http://www.medworm.com/index.php?rid=5440339&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fn02485t7n3856036%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The standard treatment of patients with high-grade gliomas based on conformal radiation therapy (RT) with or without chemotherapy
 (CT) may induce endocrine deficiencies of pituitary and subsequently also of peripheral hormones. In 24 premenopausal women
 with high-grade gliomas treated with RT and CT, hormonal changes and their impact on quality of life were investigated. Serum
 concentrations of gonadal, pituitary and of thyroid hormones were measured at various time points after initial anti-neoplastic
 therapy. Additionally, endovaginal ultrasound was performed and patients’ quality of life (QLQ) and female role functioning
 were assessed. Of 24 patients, 23 (96%) reported a change in their menstrual pattern. Twenty-one patients reported at least
 transient amenor...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5440339</comments>
            <pubDate>Sat, 19 Nov 2011 16:54:50 +0100</pubDate>
            <guid isPermaLink="false">5440339</guid>        </item>
        <item>
            <title>Higher topoisomerase 2 alpha gene transcript levels predict better prognosis in GBM patients receiving temozolomide chemotherapy: identification of temozolomide as a TOP2A inhibitor</title>
            <link>http://www.medworm.com/index.php?rid=5431349&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F2030l508028l5100%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The search for molecular markers which predict response to chemotherapy is an important aspect of current neuro-oncology research.
 MGMT promoter methylation is the only proved marker of glioblastoma. The purpose of this study was to assess the effect of
 topoisomerase expression on glioblastoma survival and study the mechanisms involved. The transcript levels of all isoforms
 of the topoisomerase family in all grades of diffuse astrocytoma were assessed. A prospective study of patients with glioblastoma
 treated by a uniform treatment procedure was performed with the objective of correlating outcome with gene expression. The
 ability of TOP2A enzyme to relax the super coiled plasmid DNA in the presence of temozolomide was evaluated to assess its
 effect on TOP2A. The t...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5431349</comments>
            <pubDate>Fri, 18 Nov 2011 17:32:22 +0100</pubDate>
            <guid isPermaLink="false">5431349</guid>        </item>
        <item>
            <title>Serum YKL-40 following resection for cerebral glioblastoma</title>
            <link>http://www.medworm.com/index.php?rid=5431350&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F931n387j4h0q48w1%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The lack of serum biomarkers for assessing the prognosis of patients with cerebral glioblastoma multiforme (GBM) prompted
 the present study in order to evaluate the significance of serum YKL-40 values in patients operated on for glioblastoma. An
 homogeneous population of 60 patients who underwent surgical removal of GBM underwent a standard treatment (surgery, radiotherapy,
 chemotherapy in the same schedule) and standard radiological monitoring (same MRI sequences at pre-defined stages). Serum
 YKL-40 levels (Quidel Corporation, San Diego, CA) were evaluated after dividing patients into two groups on the basis of the
 extent of resection (total or sub-total) according to the MRI results obtained within 48&amp;nbsp;h following surgery. YKL-40 serum
 values, significantly ...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5431350</comments>
            <pubDate>Fri, 18 Nov 2011 17:32:21 +0100</pubDate>
            <guid isPermaLink="false">5431350</guid>        </item>
        <item>
            <title>Emerging techniques in the minimally invasive treatment and management of thoracic spine tumors</title>
            <link>http://www.medworm.com/index.php?rid=5431351&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fk2h576x546715184%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Over the past decade, the development and refinement of minimally invasive spine surgery techniques has lead to procedures
 with the potential to minimize iatrogenic and post-operative sequelae that may occur during the surgical treatment of various
 pathologies. In a similar manner, parallel advances in other current treatment technologies have led to the development of
 other minimally invasive treatments of spinal malignancies. These advances include percutaneous techniques for vertebral reconstruction,
 including vertebroplasty and kyphoplasty, the development of safe and effective spinal radiosurgery, and minimal-access spinal
 surgical procedures that allow surgeons to safely decompress and reconstruct the anterior spinal column. The advent of these
 new technique...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5431351</comments>
            <pubDate>Fri, 18 Nov 2011 07:00:57 +0100</pubDate>
            <guid isPermaLink="false">5431351</guid>        </item>
        <item>
            <title>Clinical characteristics of meningiomas assessed by 11C-methionine and 18F-fluorodeoxyglucose positron-emission tomography</title>
            <link>http://www.medworm.com/index.php?rid=5431352&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F6566367575837386%2F</link>
            <description>The objective of this study was to clarify the relationship between tumor characteristics and 11C-methionine and FDG uptake in meningiomas. For 68 meningiomas in 51 cases, 11C-methionine uptake was evaluated by measuring both mean and maximum tumor/normal (T/N) ratio for the whole area of the tumors.
 FDG uptake in 44 of those meningiomas was also analyzed. Tumor size was measured volumetrically, and tumor-doubling time was
 estimated. Histopathological evaluation was performed in 19 surgical cases. Mean and maximum T/N ratios of 11C-methionine PET were significantly higher in skull-base lesions than in non-skull-base lesions. Correlations of mean and
 maximum T/N ratio of 11C-methionine PET with tumor-doubling time, MIB-1 labeling index, microvessel density and World Health Organization g...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5431352</comments>
            <pubDate>Thu, 17 Nov 2011 06:58:55 +0100</pubDate>
            <guid isPermaLink="false">5431352</guid>        </item>
        <item>
            <title>siRNA directed against Livin inhibits tumor growth and induces apoptosis in human glioma cells</title>
            <link>http://www.medworm.com/index.php?rid=5421605&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fcw723734l776rm27%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Livin, a novel member of the human inhibitors of apoptosis protein family, plays an important role in tumor progression and
 occurrence by inhibiting cell apoptosis. It is selectively expressed in the most common human neoplasms and appears to be
 involved in tumor cell resistance to chemotherapeutic agents. The present study was designed to investigate the potential
 of using RNA interference (RNAi) technique to downregulate Livin expression, and the subsequent effect on human glioma cells.
 The results showed that knockdown of Livin expression by short interfering RNA (siRNA) significantly inhibited glioma cell
 proliferation and increased cell apoptosis through cell arrest in the G1/G0 phase of cell cycle in&amp;nbsp;vitro. Furthermore, Livin siRNA significantly suppress...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5421605</comments>
            <pubDate>Wed, 16 Nov 2011 06:49:23 +0100</pubDate>
            <guid isPermaLink="false">5421605</guid>        </item>
        <item>
            <title>The role of stereotactic radiosurgery in cavernous sinus hemangiomas: a systematic review and meta-analysis</title>
            <link>http://www.medworm.com/index.php?rid=5421606&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fe037727m706q6743%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Cavernous sinus hemangioma is a rare and complex vascular tumor. A direct microsurgical approach usually results in massive
 hemorrhage. Stereotactic radiosurgery has emerged as a treatment alternative to microsurgery. To conduct a meta-analysis assessing
 the effect and complications of stereotactic radiosurgery in cavernous sinus hemangioma, a systematic review and meta-analysis
 of all cases of cavernous hemangioma in the cavernous sinus treated with stereotactic radiosurgery was performed. The search
 revealed ten papers with a total enrollment of 59 patients. Tumor size ranged from 1.5–51.4&amp;nbsp;cm3 (mean 9.6&amp;nbsp;cm3). The mean follow-up period was 49.2&amp;nbsp;months (range 6–156&amp;nbsp;months). The most recent MR images demonstrated remarkable tumor
 shrinkage in...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5421606</comments>
            <pubDate>Tue, 15 Nov 2011 16:57:11 +0100</pubDate>
            <guid isPermaLink="false">5421606</guid>        </item>
        <item>
            <title>Complete regression of papillary tumor of the pineal region after radiation therapy: case report and review of the literature</title>
            <link>http://www.medworm.com/index.php?rid=5421607&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F62377118g1228508%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Papillary tumor of the pineal region (PTPR) is a rare neuroepithelial tumor that arises in the pineal region. The optimal
 treatment for PTPR remains controversial, as no definitive treatment strategy exists for this lesion. It is not clear whether
 aggressive surgical removal is superior to biopsy followed by radiotherapy. The majority of cases in the literature have undergone
 attempted gross total resection with a supracerebellar-infratentorial or a transcallosal-transventricular approach. In this
 report, we describe a case of PTPR in a 23&amp;nbsp;year-old male that presented as a third ventricular mass causing obstructive hydrocephalus.
 An endoscopic third ventriculostomy was performed followed by an endoscopic biopsy. Postoperative radiotherapy resulted in
 complete...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5421607</comments>
            <pubDate>Tue, 15 Nov 2011 16:57:10 +0100</pubDate>
            <guid isPermaLink="false">5421607</guid>        </item>
        <item>
            <title>Spinal cord glioneuronal tumor with neuropil-like islands with 1p/19q deletion in an adult with low-grade cerebral oligodendroglioma</title>
            <link>http://www.medworm.com/index.php?rid=5421608&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fu014795243371426%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Glioneuronal tumor with neuropil-like islands (GTNI) is considered a rare variant of astrocytoma, characterized by discrete
 aggregates of cells expressing neuronal markers that punctuate a GFAP-positive glial background. Of the 24 published GTNI
 cases, only two occurred in adult spinal cords; none occurred concurrent with another CNS tumor; and none of those tested
 exhibited the 1p/19q deletion typical of oligodendroglioma. A 48-year-old man without significant past medical history was
 diagnosed with a WHO grade II oligodendroglioma by stereotactic biopsy of a lesion discovered after the patient suffered a
 generalized tonic-clonic seizure. By FISH analysis, this tumor exhibited the 1p/19q deletion present in up to 80% of oligodendrogliomas.
 The patient received 14...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5421608</comments>
            <pubDate>Mon, 14 Nov 2011 16:56:03 +0100</pubDate>
            <guid isPermaLink="false">5421608</guid>        </item>
        <item>
            <title>Imaging of human mesenchymal stromal cells: homing to human brain tumors</title>
            <link>http://www.medworm.com/index.php?rid=5407116&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fl0ng460k41l22627%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Human mesenchymal stromal cells (hMSC) can be used as a drug delivery vehicle for the treatment of GBM. However, tracking
 the migration and distribution of these transplanted cells is necessary to interpret therapeutic efficacy. We compared three
 labeling techniques for their ability to track the migration of transplanted hMSC in an orthotopic mouse xenograft model.
 hMSC were labeled with three different imaging tags (fluorescence, luciferase or ferumoxide) for imaging by fluorescence,
 bioluminescence or magnetic resonance imaging (MRI), respectively. hMSC were labeled for all imaging modalities without the
 use of transfection agents. The labeling efficacy of the tags was confirmed, followed by in vitro and in vivo migration assays
 to track hMSC migration towards ...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5407116</comments>
            <pubDate>Sat, 12 Nov 2011 06:47:36 +0100</pubDate>
            <guid isPermaLink="false">5407116</guid>        </item>
        <item>
            <title>Tandem high-dose chemotherapy and autologous stem cell transplantation for anaplastic ependymoma in children younger than 3 years of age</title>
            <link>http://www.medworm.com/index.php?rid=5407117&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fx5x81166787q2553%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The present study evaluates the feasibility and effectiveness of tandem high-dose chemotherapy and autologous stem cell transplantation
 (HDCT/autoSCT) in very young children with anaplastic ependymoma. We aimed both to improve survival and to avoid unacceptable
 late adverse effects of radiation therapy (RT) by avoiding or deferring RT until 3&amp;nbsp;years of age. Five consecutive patients
 younger than 3&amp;nbsp;years of age with anaplastic ependymoma were enrolled from April 2006 to November 2008. Tandem HDCT/autoSCT
 was given following six cycles of induction chemotherapy. RT was either not given or deferred until 3&amp;nbsp;years of age if the
 patient was in complete response after tandem HDCT/autoSCT. Median age at diagnosis was 16 (range 12–28) months. Four patients
 ...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5407117</comments>
            <pubDate>Fri, 11 Nov 2011 16:45:50 +0100</pubDate>
            <guid isPermaLink="false">5407117</guid>        </item>
        <item>
            <title>Relation between bevacizumab dose intensity and high-grade glioma survival: a retrospective study in two large cohorts</title>
            <link>http://www.medworm.com/index.php?rid=5407118&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fv55469v2p7583562%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Bevacizumab is one of the rare drugs that could improve high-grade glioma outcome after failure of chemoradiotherapy. However,
 to date, there is no biomarker predictive for efficacy of bevacizumab therapy in terms of survival improvement for patients
 with high-grade glioma. We performed a retrospective analysis of clinical factors associated with patient survival using a
 training cohort of 110 consecutive patients treated with bevacizumab for recurrent high-grade glioma and an independent validation
 cohort of 109 patients. In the training cohort, 110 consecutive patients received bevacizumab-based therapy. The number of
 chemotherapy cycles delivered was 1,411. Median follow-up was 12&amp;nbsp;months. Thirty-four patients (31%) had objective partial
 response and 24% ha...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5407118</comments>
            <pubDate>Thu, 10 Nov 2011 16:55:18 +0100</pubDate>
            <guid isPermaLink="false">5407118</guid>        </item>
        <item>
            <title>Sporadic CNS hemangioblastomatosis, response to sunitinib and secondary polycythemia</title>
            <link>http://www.medworm.com/index.php?rid=5407119&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F44157r875gh24j14%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorPages 1-2DOI 10.1007/s11060-011-0752-9Authors
		German Reyes-Botero, AP-HP, Groupe Hospitalier Pitié-Salpêtrière, Service de Neurologie Mazarin, Hôpital de la Salpêtrière, 47 Bd de l’Hôpital, 75013 Paris, FranceJaime Gallego Pérez-Larraya, AP-HP, Groupe Hospitalier Pitié-Salpêtrière, Service de Neurologie Mazarin, Hôpital de la Salpêtrière, 47 Bd de l’Hôpital, 75013 Paris, FranceMarc Sanson, AP-HP, Groupe Hospitalier Pitié-Salpêtrière, Service de Neurologie Mazarin, Hôpital de la Salpêtrière, 47 Bd de l’Hôpital, 75013 Paris, France
	

	
		Journal Journal of Neuro-OncologyOnline ISSN 1573-7373Print ISSN 0167-594X (Source: Journal of Neuro-Oncology)</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5407119</comments>
            <pubDate>Thu, 10 Nov 2011 16:55:17 +0100</pubDate>
            <guid isPermaLink="false">5407119</guid>        </item>
        <item>
            <title>Multifocal presentation of medulloblastoma in adulthood</title>
            <link>http://www.medworm.com/index.php?rid=5407120&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F3051115571652u10%2F</link>
            <description>We present a short case-illustrated review on these remarkable issues.
 
 
	Content Type Journal ArticleCategory Topic ReviewPages 1-5DOI 10.1007/s11060-011-0746-7Authors
		Pietro Ciccarino, Department of Neurosurgery, Padua University Hospital, Via Giustiniani 2, Azienda Ospedaliera di Padova, 35128 Padua, ItalyAntonino Rotilio, Department of Neurosurgery, Padua University Hospital, Via Giustiniani 2, Azienda Ospedaliera di Padova, 35128 Padua, ItalyMarta Rossetto, Department of Neuroscience, Padua University Hospital, Padua, ItalyRenzo Manara, Department of Neuro-Radiology, Padua University Hospital, Padua, ItalyEnrico Orvieto, Department of Pathology, Padua University Hospital, Padua, ItalyFranco Berti, Department of Radiotherapy, IOV IRCCS of Padua, Padua, ItalyGiuseppe Lombardi, Depar...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5407120</comments>
            <pubDate>Thu, 10 Nov 2011 06:45:35 +0100</pubDate>
            <guid isPermaLink="false">5407120</guid>        </item>
        <item>
            <title>Combined gene expression and protein interaction analysis of dynamic modularity in glioma prognosis</title>
            <link>http://www.medworm.com/index.php?rid=5407121&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fb52506ul1g445481%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Because of the variety of factors affecting glioma prognosis, prediction of patient survival is particularly difficult. Protein–protein
 interaction (PPI) networks have been considered with regard to how their spatial characteristics relate to glioma. However,
 the dynamic nature of PPIs in vivo makes them temporally and spatially complex events. Integration of prognosis-specific co-expression
 information adds further dynamic features to these networks. Although some biomarkers for glioma prognosis have been identified,
 none is sufficient for accurate prediction of either prognosis or improved survival. We have established co-expressed protein-interaction
 networks that integrate protein–protein interactions with glioma gene-expression profiles related to differen...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5407121</comments>
            <pubDate>Wed, 09 Nov 2011 17:58:59 +0100</pubDate>
            <guid isPermaLink="false">5407121</guid>        </item>
        <item>
            <title>Salvage gamma knife stereotactic radiosurgery followed by bevacizumab for recurrent glioblastoma multiforme: a case–control study</title>
            <link>http://www.medworm.com/index.php?rid=5384555&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fn30v1241w6832qn1%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;We evaluated the efficacy and safety of gamma knife stereotactic radiosurgery (GKSR) followed by bevacizumab combined with
 chemotherapy in 11 patients with recurrent glioblastoma multiforme who experienced tumor progression despite aggressive initial
 multi-modality treatment. Our experience included eight male and three female patients. The median patient age at GKSR was
 62&amp;nbsp;years (range 46–72&amp;nbsp;years). At the time of GKSR, seven patients had a first recurrence and four had two or more recurrences.
 The median interval from the initial diagnosis until GKSR was 17&amp;nbsp;months (range 5–34.5&amp;nbsp;months). The median tumor volume was
 13.6&amp;nbsp;cm3 (range 1.2–45.1&amp;nbsp;cm3) and the median margin dose of GKSR was 16&amp;nbsp;Gy (range 13–18&amp;nbsp;Gy). Following ...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5384555</comments>
            <pubDate>Fri, 04 Nov 2011 16:48:07 +0100</pubDate>
            <guid isPermaLink="false">5384555</guid>        </item>
        <item>
            <title>Growth inhibition of malignant glioblastoma by DING protein</title>
            <link>http://www.medworm.com/index.php?rid=5384556&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fetu3277j0k57h681%2F</link>
            <description>In this study, we have evaluated the effect of p38SJ, a novel member of the DING family of proteins, derived from Hypericum perforatum calluses, on the growth of malignant glioma cell lines, T98G and U-87MG by focusing on cell cycle and signaling pathways
 controlled by phosphorylation of various regulatory proteins including ERK. p38SJ, which exhibits profound phosphatase activity,
 shows the capacity to affect the phosphorylation status of several important kinases modulating signaling pathways, and cell
 growth and proliferation. Our results demonstrate that p38SJ reduces glioma cell viability and arrests cell cycle progression
 at G0/G1. The observed growth inhibitory effect of p38SJ is likely mediated by the downregulation of several cell cycle gatekeeper
 proteins, including cyclin E...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5384556</comments>
            <pubDate>Fri, 04 Nov 2011 05:43:56 +0100</pubDate>
            <guid isPermaLink="false">5384556</guid>        </item>
        <item>
            <title>Convection-enhanced delivery catheter placements for high-grade gliomas: complications and pitfalls</title>
            <link>http://www.medworm.com/index.php?rid=5384557&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fm837404u12r50753%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Convection-enhanced delivery (CED) of compounds into brain tumors reportedly circumvents the blood brain barrier. CED intends
 to increase drug delivery to malignant cells, reaching high local therapeutic concentration and decreasing or eliminating
 systemic side effects. Clinical experience and published data on catheter placement (CP) surgery are scarce. We propose practical
 and technical guidelines for planning CED based on our experience. We retrospectively analyzed the medical charts and relevant
 neuroimages of 25 patients following the insertion of 64 CED catheters. The patients were enrolled in at least one of four
 clinical trials using CED for treating recurrent glioblastoma multiforme in our institution between 2003–2006. Intra- and
 postoperative complica...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5384557</comments>
            <pubDate>Fri, 04 Nov 2011 05:43:53 +0100</pubDate>
            <guid isPermaLink="false">5384557</guid>        </item>
        <item>
            <title>Increased tryptophan transport in epileptogenic dysembryoplastic neuroepithelial tumors</title>
            <link>http://www.medworm.com/index.php?rid=5384558&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fm0154077788648u4%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Dysembryoplastic neuroepithelial tumors (DNTs) are typically hypometabolic but can show increased amino acid uptake on positron
 emission tomography (PET). To better understand mechanisms of amino acid accumulation in epileptogenic DNTs, we combined quantitative
 α-[11C]methyl-l-tryptophan (AMT) PET with tumor immunohistochemistry. Standardized uptake values (SUVs) of AMT and glucose were measured
 in 11 children with temporal lobe DNT. Additional quantification for AMT transport and metabolism was performed in 9 DNTs.
 Tumor specimens were immunostained for the l-type amino acid transporter 1 (LAT1) and indoleamine 2,3-dioxygenase (IDO), a key enzyme of the immunomodulatory kynurenine
 pathway. All 11 tumors showed glucose hypometabolism, while mean AMT SUVs were high...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5384558</comments>
            <pubDate>Thu, 03 Nov 2011 05:54:34 +0100</pubDate>
            <guid isPermaLink="false">5384558</guid>        </item>
        <item>
            <title>A phase II study of the Ras-MAPK signaling pathway inhibitor TLN-4601 in patients with glioblastoma at first progression</title>
            <link>http://www.medworm.com/index.php?rid=5384559&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F5hp58l872j641516%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;This phase II trial was undertaken to evaluate the efficacy of TLN-4601 in patients with glioblastoma (GBM) at first progression.
 TLN-4601 inhibits the Ras-MAPK signaling pathway, and in animal models crosses the blood–brain barrier and accumulates in
 implanted gliomas, possibly by binding specifically to the peripheral benzodiazepine receptor. A maximum of 40 patients with
 recurrent GBM were to be enrolled in this study. TLN-4601 was administered at a dose of 480&amp;nbsp;mg/m2/day by continuous intravenous (CIV) administration. Each 21-day cycle consisted of a 14-day CIV administration and a 7-day
 recovery period. Samples were obtained from all patients for pharmacokinetic evaluations (PK) and for Raf-1 and pERK biomarker
 assessment using immunohistochemistry and f...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5384559</comments>
            <pubDate>Thu, 03 Nov 2011 05:54:33 +0100</pubDate>
            <guid isPermaLink="false">5384559</guid>        </item>
        <item>
            <title>Glioblastoma survival in the United States before and during the temozolomide era</title>
            <link>http://www.medworm.com/index.php?rid=5384560&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fr46781t1712212l8%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The standard-of-care treatment for newly diagnosed glioblastoma changed in 2005, when radiation therapy plus temozolomide
 chemotherapy replaced radiation therapy alone. It is not yet clear how this change in treatment has influenced patient survival
 in routine clinical practice, or if a survival benefit extends to patients older than those enrolled in the trial. Data from
 the Surveillance, Epidemiology, and End Results (SEER) Program was analyzed to compare survival of adult glioblastoma patients
 diagnosed from 2000–2003 to patients diagnosed from 2005–2008, in order to evaluate pre-temozolomide and post-temozolomide
 periods. The Kaplan–Meier method and Cox proportional hazards models were used. 6,673 patients with glioblastoma diagnosed
 from 2000–2003 and...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5384560</comments>
            <pubDate>Tue, 01 Nov 2011 16:52:57 +0100</pubDate>
            <guid isPermaLink="false">5384560</guid>        </item>
        <item>
            <title>Valproic acid sensitizes human glioma cells for temozolomide and γ-radiation</title>
            <link>http://www.medworm.com/index.php?rid=5359962&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F9766407362137465%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Temozolomide (TMZ) is given in addition to radiotherapy in glioma patients, but its interaction with the commonly prescribed
 antiepileptic drug valproic acid (VPA) is largely unknown. Induction of DNA demethylation by VPA could potentially induce
 expression of the O6-methylguanine-DNA-methyltransferase (MGMT) protein, causing resistance to TMZ and thereby antagonizing its effect. Therefore,
 this study investigates the interaction between VPA, TMZ, and γ-radiation. Two glioma cell lines were used that differ in
 TMZ sensitivity caused by the absence (D384) or presence (T98) of the MGMT protein. VPA was administered before (24/48&amp;nbsp;h)
 or after (24&amp;nbsp;h) single doses of γ-radiation; or, after 24&amp;nbsp;h, VPA treatment was accompanied by a single dose of TMZ for a...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5359962</comments>
            <pubDate>Fri, 28 Oct 2011 17:24:08 +0100</pubDate>
            <guid isPermaLink="false">5359962</guid>        </item>
        <item>
            <title>Primary central nervous system post-transplant lymphoproliferative disorders following allogeneic hematopoietic stem cell transplantation</title>
            <link>http://www.medworm.com/index.php?rid=5359961&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fr12628p761m73621%2F</link>
            <description>We report a patient who developed Epstein-Barr
 virus related primary CNS-PTLD following allogeneic HSCT who was treated with the monoclonal anti-CD20 antibody rituximab
 and reduction of immunosuppression. In addition, we review the literature and discuss treatment options for patients with
 primary CNS-PTLD following allogeneic HSCT.
 
 
	Content Type Journal ArticleCategory Topic ReviewPages 1-8DOI 10.1007/s11060-011-0739-6Authors
		Frank Lieberman, Divisions of Hematology-Oncology, and Hematopathology, University of Pittsburgh Cancer Institute, University of Pittsburgh School of Medicine, 5150 Center Ave., Suite. 572, Pittsburgh, PA 15232, USAVictor Yazbeck, Divisions of Hematology-Oncology, and Hematopathology, University of Pittsburgh Cancer Institute, University of Pittsburgh School...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5359961</comments>
            <pubDate>Fri, 28 Oct 2011 17:24:08 +0100</pubDate>
            <guid isPermaLink="false">5359961</guid>        </item>
        <item>
            <title>Tumorigenesis and prognostic role of hepatoma-derived growth factor in human gliomas</title>
            <link>http://www.medworm.com/index.php?rid=5359960&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F26258r7801652901%2F</link>
            <description>In this study, we found a significant incidence of HDGF prevalence between the different pathological types and stages of
 glioma in 105 patients. We also found a prognostic significance in 41 glioblastoma multiforme (GBM) patients, with prevalence
 of nuclear HDGF predicting short survival of patients with GBM after surgery. To delineate the mitogenic role of HDGF in gliomagenesis,
 an adenoviral-expressed HDGF small interfering RNA (Ad-HDGF siRNA) was used to knock down expression of nuclear HDGF. After
 knocking down nuclear HDGF expression in human GBM cells, cell growth and cell invasion and induction on apoptosis by caspase-3
 activation were significantly inhibited. We conclude that HDGF is a mitogenic growth factor in glioma progression and can
 be a useful prognostic marker for GB...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5359960</comments>
            <pubDate>Fri, 28 Oct 2011 17:24:08 +0100</pubDate>
            <guid isPermaLink="false">5359960</guid>        </item>
        <item>
            <title>Non-invasive detection of 2-hydroxyglutarate and other metabolites in IDH1 mutant glioma patients using magnetic resonance spectroscopy</title>
            <link>http://www.medworm.com/index.php?rid=5346885&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fg6211644vt468412%2F</link>
            <description>In conclusion, water-suppressed proton (1H) MRS provides a non-invasive measure of 2-HG in gliomas, and may serve as a potential biomarker for patients with IDH1 mutant brain tumors. In addition to 2-HG, alterations in several other metabolites measured by MRS correlate with IDH1 mutation status.
 
 
	Content Type Journal ArticleCategory Clinical Study – Patient StudyPages 1-9DOI 10.1007/s11060-011-0737-8Authors
		Whitney B. Pope, Department of Radiological Sciences, David Geffen School of Medicine at UCLA, University of California at Los Angeles, Los Angeles, CA 90095, USARobert M. Prins, Department of Neurosurgery, David Geffen School of Medicine at UCLA, University of California at Los Angeles, Gonda Building, Room 3357, 695 Charles Young Drive, Los Angeles, CA 90095-1761, USAM. Alber...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5346885</comments>
            <pubDate>Fri, 21 Oct 2011 05:48:27 +0100</pubDate>
            <guid isPermaLink="false">5346885</guid>        </item>
        <item>
            <title>Erratum to: Temozolomide and 13-cis retinoic acid in patients with anaplastic gliomas: a prospective single-arm monocentric phase-II study (RNOP-05)</title>
            <link>http://www.medworm.com/index.php?rid=5335135&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F846t23p1158k4326%2F</link>
            <description>Content Type Journal ArticleCategory ErratumPages 1-1DOI 10.1007/s11060-011-0742-yAuthors
		Oliver Grauer, Department of Neurology, University Medical Center Regensburg, Universitätsstrasse 84, 93053 Regensburg, GermanyChristina Pascher, Department of Neurology, University Medical Center Regensburg, Universitätsstrasse 84, 93053 Regensburg, GermanyChristian Hartmann, Clinical Cooperation Unit Neuropathology (G380), German Cancer Research Center, Heidelberg, GermanyFlorian Zeman, Center for Clinical Studies, University Medical Center Regensburg, Franz-Josef-Strauß-Allee 11, 93053 Regensburg, GermanyMichael Weller, Department of Neurology, University Hospital Zürich, Frauenklinikstrasse 26, 8091 Zurich, SwitzerlandMartin Proescholdt, Department of Neurosurgery, University Medical Cente...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5335135</comments>
            <pubDate>Wed, 19 Oct 2011 15:44:43 +0100</pubDate>
            <guid isPermaLink="false">5335135</guid>        </item>
        <item>
            <title>Stereotactic radiosurgery for benign meningiomas</title>
            <link>http://www.medworm.com/index.php?rid=5335136&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fvm2344567175u013%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Meningiomas are the second most common primary tumor of the brain. Surgical resection is the preferred treatment for easily
 accessible tumors that can be safely removed. However, many tumors arise deep within the skull base making complete surgical
 resection difficult or impossible. Stereotactic radiosurgery is a highly effective alternative to surgical resection that
 has been used as a primary therapy for benign meningiomas as well as an adjuvant treatment for residual or recurrent tumors.
 The 5-year tumor control rates for stereotactic radiosurgery are equivalent to gross-total resection with lower morbidity
 than surgery, especially for skull base lesions. Additionally, adjuvant treatment of subtotally resected tumors results in
 tumor control rates equivalent to...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5335136</comments>
            <pubDate>Tue, 18 Oct 2011 06:00:53 +0100</pubDate>
            <guid isPermaLink="false">5335136</guid>        </item>
        <item>
            <title>Genomic profiling of glioblastoma: convergence of fundamental biologic tenets and novel insights</title>
            <link>http://www.medworm.com/index.php?rid=5323656&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fa966661445kg6725%2F</link>
            <description>This article will review how the glioblastoma genomic data
 set serves as an illustrative platform for the concepts put forward by Hanahan and Weinberg on the cancer phenotype. The picture
 emerging suggests that most glioblastomas evolve along a multitude of pathways rather than a single defined pathway. In this
 context, the article will further provide a discussion of the subtypes of glioblastoma as they relate to key principles of
 developmental neurobiology.
 
 
	Content Type Journal ArticleCategory Topic ReviewPages 1-12DOI 10.1007/s11060-011-0714-2Authors
		Kimberly Ng, Department of Radiation Oncology, Dana-Farber Cancer Institute, Boston, MA, USARyan Kim, Department of Neurology, Moores UCSD Cancer Center, University of California, San Diego, La Jolla, CA, USASantosh Kesari, Depar...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5323656</comments>
            <pubDate>Sat, 15 Oct 2011 05:49:39 +0100</pubDate>
            <guid isPermaLink="false">5323656</guid>        </item>
        <item>
            <title>Outcome after bevacizumab clinical trial therapy among recurrent grade III malignant glioma patients</title>
            <link>http://www.medworm.com/index.php?rid=5323657&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F884144qq421qp820%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Although outcome following bevacizumab among recurrent grade IV malignant glioma patients is documented as poor by several
 analyses, outcome for recurrent grade III patients following bevacizumab therapy has not been specifically evaluated. We performed
 a pooled analysis of 96 recurrent grade III malignant glioma patients enrolled on three consecutive phase II bevacizumab salvage
 trials to evaluate overall outcome following bevacizumab trial discontinuation. Outcome on the three bevacizumab trials, which
 included similar eligibility, treatment and assessment criteria, was comparable. Forty-nine patients who progressed on bevacizumab
 trial therapy and remained alive for at least 30&amp;nbsp;days elected to receive additional therapy. These patients achieved a median
 PF...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5323657</comments>
            <pubDate>Fri, 14 Oct 2011 05:48:16 +0100</pubDate>
            <guid isPermaLink="false">5323657</guid>        </item>
        <item>
            <title>Central nervous system metastases from castration-resistant prostate cancer in the docetaxel era</title>
            <link>http://www.medworm.com/index.php?rid=5313875&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fg2q55rw338031836%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Central nervous system (brain or leptomeningeal) metastases (BLm) are considered rare in castration-resistant prostate cancer
 (CRPC) patients. Now that docetaxel has become the reference drug for first-line treatment of CRPC, patients whose disease
 is not controlled by hormonal manipulations may live much longer than before and have higher risk of developing BLm. We retrospectively
 reviewed the records of all patients with CRPC attending our centres from 2002 to 2010, and identified all of those who were
 diagnosed as having BLm and received (or were considered to have been eligible to receive) docetaxel-based treatment. We identified
 31 cases of BLm (22 brain metastases and 9 leptomeningeal metastases) with an incidence of 3.3%. BLm-free survival was 43.5&amp;nbsp;mont...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5313875</comments>
            <pubDate>Wed, 12 Oct 2011 05:50:34 +0100</pubDate>
            <guid isPermaLink="false">5313875</guid>        </item>
        <item>
            <title>Phase II study of carboplatin, irinotecan, and bevacizumab for bevacizumab naïve, recurrent glioblastoma</title>
            <link>http://www.medworm.com/index.php?rid=5313876&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F56l3u41063k4m614%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;We evaluated the efficacy of carboplatin, irinotecan, and bevacizumab among bevacizumab-naïve, recurrent glioblastoma (GBM)
 patients in a phase 2, open-label, single arm trial. Forty eligible patients received carboplatin (area under the plasma curve
 [AUC] 4&amp;nbsp;mg/ml-min) on day one, while bevacizumab (10&amp;nbsp;mg/kg) and irinotecan (340&amp;nbsp;mg/m2 for patients on CYP3A-enzyme-inducing anti-epileptics [EIAEDs] and 125&amp;nbsp;mg/m2 for patients not on EIAEDs) were administered on days 1 and 14 of every 28-day cycle. Patients were evaluated after each
 of the first two cycles and then after every other cycle. Treatment continued until progressive disease, unacceptable toxicity,
 non-compliance, or voluntary withdrawal. The primary endpoint was progression-free survival ...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5313876</comments>
            <pubDate>Tue, 11 Oct 2011 05:51:40 +0100</pubDate>
            <guid isPermaLink="false">5313876</guid>        </item>
        <item>
            <title>Improved survival time trends for glioblastoma using the SEER 17 population-based registries</title>
            <link>http://www.medworm.com/index.php?rid=5313877&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fv41326u8312072t2%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The EORTC/NCIC 22981/26981 study demonstrated an improvement in median overall survival (OS) from 12.1 to 14.6&amp;nbsp;months in patients
 with glioblastoma (GBM) who received temozolomide with post-operative radiotherapy (RT). The current study was performed to
 determine if those results translated into a survival benefit in a population-based cohort. Patients diagnosed between 2000
 and 2006 with a GBM who underwent surgery and post-operative RT were selected from the Surveillance, Epidemiology and End
 Results database. Patients were grouped into time periods: 2000–2001, 2002–2003, 2004 and 2005–2006 (which represented those
 treated after the EORTC/NCIC trial presentation in 2004). Relative survival (RS) was estimated by the Kaplan–Meier method,
 and Cox multi...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5313877</comments>
            <pubDate>Sat, 08 Oct 2011 15:44:19 +0100</pubDate>
            <guid isPermaLink="false">5313877</guid>        </item>
        <item>
            <title>HMGA1 expression in human gliomas and its correlation with tumor proliferation, invasion and angiogenesis</title>
            <link>http://www.medworm.com/index.php?rid=5313879&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fj30204n7w7402865%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;High-mobility group A1 (HMGA1) protein is an architectural transcription factor widely expressed during embryonic development
 and tumor progression. The purpose of this research was to investigate the expression of HMGA1 in malignant gliomas with different
 WHO classification and to study the correlation of HMGA1 expression with tumor proliferation, invasion, and angiogenesis.
 Expression of HMGA1, Ki-67, MMP-9, VEGF-A, and MVD in malignant gliomas and their correlation were studied in 60 samples of
 different WHO classification by use of immunohistochemistry, and in 27 randomly selected samples by use of real-time quantitative
 PCR. Immunohistochemistry results showed that nuclear immunostaining of HMGA1 protein was not observed in normal brain tissues
 but was observ...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5313879</comments>
            <pubDate>Sat, 08 Oct 2011 05:52:22 +0100</pubDate>
            <guid isPermaLink="false">5313879</guid>        </item>
        <item>
            <title>Phase I study of panobinostat in combination with bevacizumab for recurrent high-grade glioma</title>
            <link>http://www.medworm.com/index.php?rid=5313878&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ft8r1615667004235%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Bevacizumab is frequently used to treat patients with recurrent high-grade glioma (HGG), but responses are generally not durable.
 Panobinostat is a histone deacetylase inhibitor with anti-neoplastic and anti-angiogenic effects and may work synergistically
 with VEGF inhibitors. We performed a phase I study to evaluate the safety and tolerability of the combination of orally administered
 panobinostat with bevacizumab in patients with recurrent HGG. Patients with recurrent HGG were treated on a 3&amp;nbsp;+&amp;nbsp;3 trial design.
 Patients received bevacizumab 10&amp;nbsp;mg/kg every other week in combination with oral panobinostat. The starting dose of panobinostat
 was 20&amp;nbsp;mg three times per week, weekly (cohort 1). Due to concerns for thrombocytopenia with the weekly dosin...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5313878</comments>
            <pubDate>Sat, 08 Oct 2011 05:52:22 +0100</pubDate>
            <guid isPermaLink="false">5313878</guid>        </item>
        <item>
            <title>Expression of dual angiogenic/neurogenic growth factors in human primary brain tumors</title>
            <link>http://www.medworm.com/index.php?rid=5304083&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fm27h3666750jptg4%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Brain tumors, benign or malignant, are characterized by a very high degree of vascularization. Recent accumulating evidence
 suggests that during development the neuronal wiring follows the same routes as the vasculature and that these two systems
 may share some of the same factors for guidance. Thus, expression of dual angiogenic/neurogenic growth factors was evaluated
 by in&amp;nbsp;situ hybridization in human primary brain tumors of three different types, i.e., astrocytomas, oligodendrogliomas, and
 ependymomas, of increasing grades, in relation with the grade and type of the tumor. For this evaluation we selected vascular
 endothelial growth factor (VEGF-A) and its receptors VEGF-R1 and VEGF-R2 and the neuropilins&amp;nbsp;1 and 2 (NRP-1 and NRP-2), which
 have proangioge...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5304083</comments>
            <pubDate>Fri, 07 Oct 2011 05:44:52 +0100</pubDate>
            <guid isPermaLink="false">5304083</guid>        </item>
        <item>
            <title>Novel amplifications in pediatric medulloblastoma identified by genome-wide copy number profiling</title>
            <link>http://www.medworm.com/index.php?rid=5304084&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F5108kk254802834g%2F</link>
            <description>In this study, we profiled a series of 25 MB with a
 32K BAC array covering 99% of the current assembly of the human genome for the identification of genetic copy number alterations
 possibly important in MB. Previously known aberrations as well as several novel focally amplified loci could be identified.
 As expected, the most frequently observed alteration was the combination of 17p loss and 17q gain, which was detected in both
 high- and standard-risk patients. We also defined minimal overlapping regions of aberrations, including 16 regions of gain
 and 18 regions of loss in various chromosomes. A few noteworthy narrow amplified loci were identified on autosomes&amp;nbsp;1 (38.89–41.97
 and 84.89–90.76&amp;nbsp;Mb), 3 (27.64–28.20 and 35.80–43.50&amp;nbsp;Mb), and 8 (119.66–139.79&amp;nbsp;Mb...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5304084</comments>
            <pubDate>Fri, 07 Oct 2011 05:44:51 +0100</pubDate>
            <guid isPermaLink="false">5304084</guid>        </item>
        <item>
            <title>Protein alterations associated with temozolomide resistance in subclones of human glioblastoma cell lines</title>
            <link>http://www.medworm.com/index.php?rid=5304085&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fc5753m760520r717%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Temozolomide (TMZ) is the standard chemotherapeutic agent for human malignant glioma, but intrinsic or acquired chemoresistance
 represents a major obstacle to successful treatment of this highly lethal group of tumours. Obtaining better understanding
 of the molecular mechanisms underlying TMZ resistance in malignant glioma is important for the development of better treatment
 strategies. We have successfully established a passage control line (D54-C10) and resistant variants (D54-P5 and D54-P10)
 from the parental TMZ-sensitive malignant glioma cell line D54-C0. The resistant sub-cell lines showed alterations in cell
 morphology, enhanced cell adhesion, increased migration capacities, and cell cycle arrests. Proteomic analysis identified
 a set of proteins that showed...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5304085</comments>
            <pubDate>Fri, 07 Oct 2011 05:44:50 +0100</pubDate>
            <guid isPermaLink="false">5304085</guid>        </item>
        <item>
            <title>Cerebrospinal fluid stimulates leptomeningeal and meningioma cell proliferation and activation of STAT3</title>
            <link>http://www.medworm.com/index.php?rid=5296594&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fm071m603g5626861%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The role of cerebrospinal fluid (CSF) in the pathogenesis of meningiomas is unknown. Cell cultures from three human leptomeninges,
 five WHO grade I and seven grade II meningiomas were treated with remnant CSF from 22 patients with no central nervous system
 disease and normal cell indices. Cells were evaluated by CyQUANT for DNA synthesis/cell proliferation and by western blots
 for phosphorylation/activation of growth regulatory pathways activated in meningiomas including JAK1–STAT3, MEK1–p44/42MAPK,
 Akt–mTOR and Rb. Analysis of Caspase 3 activation and survivin was also performed. Finally, the effects of PDGF neutralizing
 antibody and cucurbitacin, a STAT3 inhibitor on CSF stimulation were tested. Compared to controls and the mitogen PDGF-BB,
 various CSF sam...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5296594</comments>
            <pubDate>Wed, 05 Oct 2011 05:48:13 +0100</pubDate>
            <guid isPermaLink="false">5296594</guid>        </item>
        <item>
            <title>Corticosteroid-use in primary and secondary brain tumour patients: a review</title>
            <link>http://www.medworm.com/index.php?rid=5296593&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fek5601246157qjk1%2F</link>
            <description>This article reviews the literature,
 specifically in relation to the role of corticosteroids in primary and secondary brain tumour patients. Areas reviewed include
 corticosteroid pharmacology, indications, mechanism of action, toxicity profile, prescribing practices, and corticosteroid-sparing
 agents.
 
 
	Content Type Journal ArticleCategory Topic ReviewPages 1-11DOI 10.1007/s11060-011-0713-3Authors
		Richella Ryan, Palliative Care Department, Elsworth House, Addenbrookes Hospital, Cambridge University Hospitals NHS Foundation Trust, Hills Road, Cambridge, CB2 0QQ UKSara Booth, Palliative Care Department, Elsworth House, Addenbrookes Hospital, Cambridge University Hospitals NHS Foundation Trust, Hills Road, Cambridge, CB2 0QQ UKStephen Price, University of Cambridge, Cambridge, UK
	

	...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5296593</comments>
            <pubDate>Wed, 05 Oct 2011 05:48:13 +0100</pubDate>
            <guid isPermaLink="false">5296593</guid>        </item>
        <item>
            <title>Erratum to: Oxcarbazepine monotherapy in patients with brain tumor-related epilepsy: open-label pilot study for assessing the efficacy, tolerability and impact on quality of life</title>
            <link>http://www.medworm.com/index.php?rid=5296596&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fc517830370110066%2F</link>
            <description>Content Type Journal ArticleCategory ErratumPages 1-3DOI 10.1007/s11060-011-0732-0Authors
		M. Maschio, Department of Neuroscience and Cervical-Facial Pathology, Center for Tumor-related Epilepsy, National Institute for Cancer, “Regina Elena”, Via Elio Chianesi 53, 00144 Rome, ItalyL. Dinapoli, Department of Neuroscience and Cervical-Facial Pathology, Center for Tumor-related Epilepsy, National Institute for Cancer, “Regina Elena”, Via Elio Chianesi 53, 00144 Rome, ItalyF. Sperati, Department of Epidemiology, National Institute for Cancer, “Regina Elena”, Via Elio Chianesi 53, 00144 Rome, ItalyA. Fabi, Department of Oncology, National Institute for Cancer, “Regina Elena”, Via Elio Chianesi 53, 00144 Rome, ItalyA. Pace, Department of Neuroscience and Cervical-Facial Pathol...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5296596</comments>
            <pubDate>Wed, 05 Oct 2011 05:48:12 +0100</pubDate>
            <guid isPermaLink="false">5296596</guid>        </item>
        <item>
            <title>Ion channels in pediatric CNS Atypical Teratoid/Rhabdoid Tumor (AT/RT) cells: potential targets for novel therapeutic agents</title>
            <link>http://www.medworm.com/index.php?rid=5296595&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fl848673667844545%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The central nervous system Atypical Teratoid/Rhabdoid Tumor (CNS AT/RT) is a highly malignant neoplasm that commonly affects
 infants and young children, and has an extremely poor prognosis. Recently, a small subset of ion channels have been found
 to be over-expressed in a variety of malignant cells, thus emerging as potential therapeutic targets for difficult to treat
 tumors. We have studied the electrophysiological properties of AT/RT cell lines with particular attention to cell volume sensitive
 ion channels (VSC). This class of membrane proteins can play a fundamental role in cellular processes relevant to tumor development.
 We have found that chloride selective VSCs are particularly active in AT/RT cell lines, compared to non-tumor cells. We evaluated
 specific ...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5296595</comments>
            <pubDate>Wed, 05 Oct 2011 05:48:12 +0100</pubDate>
            <guid isPermaLink="false">5296595</guid>        </item>
        <item>
            <title>The burden of brain tumor: a single-institution study on psychological patterns in caregivers</title>
            <link>http://www.medworm.com/index.php?rid=5296597&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F955tr354h657v954%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Quality of life and well-being in caregivers are usually partly neglected since all attention is focused on patients and the
 way they react to the illness. Carers also usually neglect their own needs, especially when the illness of the patient is
 as complex as a brain tumor. The aim of this study is to investigate how caregivers deal with a diagnosis of brain tumor in
 their relatives and how they manage their quality of life and psychosocial well-being. One hundred primary caregivers of patients
 with brain tumors were interviewed and were asked to fill in self–administered questionnaires detecting multidimensional levels
 of quality of life, anxiety, depression, and psychosocial reaction to the patient’s illness. Data were related with some functional
 and psych...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5296597</comments>
            <pubDate>Tue, 04 Oct 2011 05:50:48 +0100</pubDate>
            <guid isPermaLink="false">5296597</guid>        </item>
        <item>
            <title>O6-methylguanine-DNA methyltransferase promoter methylation in 45 primary central nervous system lymphomas: quantitative assessment of methylation and response to temozolomide treatment</title>
            <link>http://www.medworm.com/index.php?rid=5296599&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fq1333r44l11172g2%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Favorable responses to temozolomide chemotherapy have recently been reported in primary central nervous system lymphoma (PCNSL)
 patients who are refractory to high-dose methotrexate therapy. The gene encoding the DNA repair enzyme O
 6-methylguanine-DNA methyltransferase (MGMT) is transcriptionally silenced by promoter methylation in several human tumors,
 including gliomas and systemic lymphomas. MGMT promoter methylation is also a prognostic marker in glioblastoma patients treated with temozolomide. To validate temozolomide
 treatment in PCNSL, we applied methylation-sensitive high resolution melting (MS-HRM) analysis to quantitate MGMT methylation in PCNSL. MGMT promoter methylation was detected in tumors from 23 (51%) of 45 PCNSL patients, 11 of which were consider...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5296599</comments>
            <pubDate>Tue, 04 Oct 2011 05:50:47 +0100</pubDate>
            <guid isPermaLink="false">5296599</guid>        </item>
        <item>
            <title>Brain biopsy is required in steroid-resistant patients with chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids (CLIPPERS)</title>
            <link>http://www.medworm.com/index.php?rid=5296598&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F16005421n0r710u3%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorPages 1-2DOI 10.1007/s11060-011-0724-0Authors
		Nadège Limousin, Department of Neurology, CHRU, 2, Boulevard Tonnellé, 37044 Tours cedex, FranceJulien Praline, Department of Neurology, CHRU, 2, Boulevard Tonnellé, 37044 Tours cedex, FranceOana Motica, Department of Neurology, CHRU, 2, Boulevard Tonnellé, 37044 Tours cedex, FranceJean Philippe Cottier, Department of Neuroradiology, CHRU, Tours, FranceCecilia Rousselot-Denis, Department of Pathology, CHRU, Tours, FranceKarima Mokhtari, Department of Pathology, Pitié Salpêtrière, Paris, FranceAlberto Gonzalez-Aguilar, Department of Neuro-oncology, Pitié Salpêtrière, Paris, FranceBertrand De Toffol, Department of Neurology, CHRU, 2, Boulevard Tonnellé, 37044 Tours cedex, Fra...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5296598</comments>
            <pubDate>Tue, 04 Oct 2011 05:50:47 +0100</pubDate>
            <guid isPermaLink="false">5296598</guid>        </item>
        <item>
            <title>A phase II study of O6-benzylguanine and temozolomide in pediatric patients with recurrent or progressive high-grade gliomas and brainstem gliomas: a Pediatric Brain Tumor Consortium study</title>
            <link>http://www.medworm.com/index.php?rid=5296600&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F88t4817714310n62%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;To estimate the sustained (≥8&amp;nbsp;weeks) objective response rate in pediatric patients with recurrent or progressive high-grade
 gliomas (HGG, Stratum A) or brainstem gliomas (BSG, Stratum B) treated with the combination of O6-benzylguanine (O6BG) and
 temozolomide® (TMZ). Patients received O6BG 120&amp;nbsp;mg/m2/d IV followed by TMZ 75&amp;nbsp;mg/m2/d orally daily for 5 consecutive days of each 28-day course. The target objective response rate to consider the combination
 active was 17%. A two-stage design was employed. Forty-three patients were enrolled; 41 were evaluable for response, including
 25 patients with HGG and 16 patients with BSG. The combination of O6BG and TMZ was tolerable, and the primary toxicities were
 myelosuppression and gastrointestinal symptoms. O...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5296600</comments>
            <pubDate>Tue, 04 Oct 2011 05:50:45 +0100</pubDate>
            <guid isPermaLink="false">5296600</guid>        </item>
        <item>
            <title>Metastatic glioblastoma: case presentations and a review of the literature</title>
            <link>http://www.medworm.com/index.php?rid=5285161&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ftp7p3g61x31481g6%2F</link>
            <description>We report two cases
 of metastatic GBM seen within an 8-week period followed by a literature review. We attempted to identify common factors or
 a causative mechanism. Factors that predominated among the reviewed cases included male gender, tumor location, and younger
 age. Causative mechanisms were not apparent. While metastatic disease remains rare, it might be occurring with increasing
 frequency. This trend might be due to increased diagnosis, better imaging, a more extensive physician workup, or an increase
 in survival. Metastatic GBM can present and progress quite rapidly, and repeat evaluations of persistent or worsening complaints
 among GBM patients are warranted. Early diagnosis of metastatic disease spread can help to expedite alleviation of patients’
 discomfort, in an alrea...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5285161</comments>
            <pubDate>Sun, 02 Oct 2011 05:46:55 +0100</pubDate>
            <guid isPermaLink="false">5285161</guid>        </item>
        <item>
            <title>A randomized trial on the efficacy of methylphenidate and modafinil for improving cognitive functioning and symptoms in patients with a primary brain tumor</title>
            <link>http://www.medworm.com/index.php?rid=5285162&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fa0671m8688758120%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Limited research is available regarding the efficacy of psychostimulants in treating cognitive function in primary brain tumor
 patients. An open-label, randomized, pilot trial examined both the general and differential efficacy of 4&amp;nbsp;weeks of methylphenidate
 (MPH) and modafinil (MOD) in 24 brain tumor patients. Participants completed cognitive tests and self-report measures of fatigue,
 sleep disturbance, mood and quality of life at baseline and after 4&amp;nbsp;weeks.
 
 
 Following stimulant treatment, there was evidence of a beneficial effect on test performance in speed of processing and executive
 function requiring divided attention. Patients with the greatest deficit in executive function at baseline appeared to derive
 the greatest benefit following stimulant ...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5285162</comments>
            <pubDate>Sun, 02 Oct 2011 05:46:54 +0100</pubDate>
            <guid isPermaLink="false">5285162</guid>        </item>
        <item>
            <title>uPAR and cathepsin B downregulation induces apoptosis by targeting calcineurin A to BAD via Bcl-2 in glioma</title>
            <link>http://www.medworm.com/index.php?rid=5285163&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fr38l1j1541613744%2F</link>
            <description>In conclusion, downregulation of uPAR
 and cathepsin B induced apoptosis by targeting calcineurin A to BAD via Bcl-2 in glioma.
 
 
	Content Type Journal ArticleCategory Laboratory Investigation - Human/Animal TissuePages 1-12DOI 10.1007/s11060-011-0727-xAuthors
		Rama Rao Malla, Department of Cancer Biology and Pharmacology, University of Illinois College of Medicine at Peoria, One Illini Drive, Peoria, IL 61605, USASreelatha Gopinath, Department of Cancer Biology and Pharmacology, University of Illinois College of Medicine at Peoria, One Illini Drive, Peoria, IL 61605, USAChristopher S. Gondi, Department of Cancer Biology and Pharmacology, University of Illinois College of Medicine at Peoria, One Illini Drive, Peoria, IL 61605, USAKiranmai Alapati, Department of Cancer Biology and Pharma...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5285163</comments>
            <pubDate>Sun, 02 Oct 2011 05:46:53 +0100</pubDate>
            <guid isPermaLink="false">5285163</guid>        </item>
        <item>
            <title>Pediatric high grade glioma of the spinal cord: results of the HIT-GBM database</title>
            <link>http://www.medworm.com/index.php?rid=5285164&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ft287273h5w684w88%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Little is known about pediatric spinal cord high grade gliomas (SCHGG) beyond their dismal prognosis. Here, we analyzed the
 HIT-GBM® database for the influence of surgical resection on survival. Between 1991 and 2010 the HIT-GBM group collected data from
 European children diagnosed with high grade glioma. Patients with the following inclusion criteria were analyzed in this study:
 astrocytic histology, WHO grade III or IV, age at diagnosis &amp;lt;18&amp;nbsp;years, and tumor localized to the spinal cord. 28 patients
 (mean age 11.28&amp;nbsp;years, 14 male) with primary SCHGG were identified. The tumor sizes were measured by the span across adjacent
 vertebrae and varied greatly (range: 1–20, median: 4). Histology was classified as WHO grade III in 15 and grade IV in 13
 tumo...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5285164</comments>
            <pubDate>Sat, 01 Oct 2011 05:45:56 +0100</pubDate>
            <guid isPermaLink="false">5285164</guid>        </item>
        <item>
            <title>The feasibility of real-time in vivo optical detection of blood–brain barrier disruption with indocyanine green</title>
            <link>http://www.medworm.com/index.php?rid=5285165&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fjv1j7p744185g180%2F</link>
            <description>This study shows the feasibility of optical monitoring
 of BBB disruption with intravenous (IV) ICG injections. Virtual real-time optical monitoring of the BBB disruption could help
 improve intraarterial delivery of chemotherapeutic drugs.
 
 
	Content Type Journal ArticleCategory Laboratory Investigation - Human/Animal TissuePages 1-10DOI 10.1007/s11060-011-0711-5Authors
		Aysegul Ergin, Department of Biomedical Engineering, Boston University, Boston, MA 02215, USAMei Wang, Department of Anesthesiology, College of Physicians and Surgeons of Columbia University, 630 West 168th Street, P&amp;S P Box 46, New York, NY 10032, USAJane Y. Zhang, Department of Biomedical Engineering, Boston University, Boston, MA 02215, USAJeffrey N. Bruce, Department of Neurosurgery, College of Physicians and Surge...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5285165</comments>
            <pubDate>Sat, 01 Oct 2011 05:45:55 +0100</pubDate>
            <guid isPermaLink="false">5285165</guid>        </item>
        <item>
            <title>Predictors of survival among older adults with ependymoma</title>
            <link>http://www.medworm.com/index.php?rid=5273229&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ft66340842667jwv1%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The biological process of aging encompasses a multitude of complex physiological and lifestyle changes that may alter the
 way typical prognostic factors affect survival among older ependymoma patients. Because very little is known about the clinical
 significance of traditional prognostic factors and the magnitude of their effects among older individuals, the purpose of
 this study was to evaluate the associations between survival and demographic and tumor characteristics among patients with
 ependymoma who were 60&amp;nbsp;years of age or older. Using the 1973–2007 dataset from the Surveillance, Epidemiology and End Results
 (SEER) program, we evaluated the impact of several factors on both overall and ependymoma-specific survival, utilizing multivariable
 Cox proportio...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5273229</comments>
            <pubDate>Wed, 28 Sep 2011 05:54:36 +0100</pubDate>
            <guid isPermaLink="false">5273229</guid>        </item>
        <item>
            <title>Evaluation of radiation necrosis and malignant glioma in rat models using diffusion tensor MR imaging</title>
            <link>http://www.medworm.com/index.php?rid=5273230&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fn7401p4873246r50%2F</link>
            <description>In this study, one delayed radiation necrosis model (dose, 40&amp;nbsp;Gy; radiation field,
 10&amp;nbsp;×&amp;nbsp;10&amp;nbsp;mm2; n&amp;nbsp;=&amp;nbsp;13) and two orthotopic glioma models in rats (9L gliosarcoma, n&amp;nbsp;=8; human glioma xenografts, n&amp;nbsp;=&amp;nbsp;5) were compared using multiple diffusion tensor imaging (DTI) indices. A visible isotropic apparent diffusion coefficient
 (ADC) pattern was observed in the lesion due to radiation necrosis, which consisted of a hypointense central zone and a hyperintense
 peripheral zone. There were significantly lower ADC, parallel diffusivity, and perpendicular diffusivity in the necrotic central
 zone than in the peripheral zone (all P&amp;nbsp;&amp;lt;&amp;nbsp;0.001). When radiation-induced necrosis was compared with viable tumor, radiation necrosis had significantly lowe...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5273230</comments>
            <pubDate>Tue, 27 Sep 2011 05:54:31 +0100</pubDate>
            <guid isPermaLink="false">5273230</guid>        </item>
        <item>
            <title>Phase II study of Gleevec® plus hydroxyurea (HU) in adults with progressive or recurrent meningioma</title>
            <link>http://www.medworm.com/index.php?rid=5260142&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fb7q5455842l46220%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;We prospectively evaluated the efficacy and safety of imatinib plus hydroxyurea in patients with progressive/recurrent meningioma.
 A total of 21 patients with progressive/recurrent meningioma were enrolled in this dual center, single-arm, phase II trial.
 All patients received 500&amp;nbsp;mg of hydroxyurea twice a day. Imatinib was administered at 400&amp;nbsp;mg/day for patients not on CYP3A
 enzyme inducing anti-epileptic drugs (EIAEDs) and at 500&amp;nbsp;mg twice a day for patients on EIAEDs. The primary endpoint was progression-free
 survival at 6&amp;nbsp;months (PFS-6) and secondary endpoints were safety, radiographic response rate, and overall survival (OS). Best
 radiographic response was stable disease and was observed in 14 patients (67%). PFS-6 for all patients, those wit...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5260142</comments>
            <pubDate>Thu, 22 Sep 2011 06:37:29 +0100</pubDate>
            <guid isPermaLink="false">5260142</guid>        </item>
        <item>
            <title>Clinical outcome of central nervous system metastases from breast cancer: differences in survival depending on systemic treatment</title>
            <link>http://www.medworm.com/index.php?rid=5260144&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fhxr10017224n3326%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Central nerve system (CNS) metastases are a feared complication of breast cancer and are associated with poor prognosis. The
 purpose of this study is to investigate the clinical characteristics of CNS metastases and to clarify the prognostic factors
 after CNS metastases in breast cancer at a single institution over a long time period. We retrospectively reviewed the medical
 records of breast cancer patients diagnosed at Seoul National University Hospital from 1981 to 2009 and identified the patients
 who experienced CNS metastases. We collected the data, including demographics, clinico-pathologic characteristics, dates of
 diagnosis of original breast cancer and subsequent metastases, and date of death, and correlated the findings with the clinical
 outcome. A total ...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5260144</comments>
            <pubDate>Thu, 22 Sep 2011 06:37:28 +0100</pubDate>
            <guid isPermaLink="false">5260144</guid>        </item>
        <item>
            <title>R-flurbiprofen, a novel nonsteroidal anti-inflammatory drug, decreases cell proliferation and induces apoptosis in pituitary adenoma cells in vitro</title>
            <link>http://www.medworm.com/index.php?rid=5260143&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fa2t5171577441652%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;R-flurbiprofen, a nonsteroidal anti-inflammatory drug derivative, has been shown to inhibit colonic adenoma formation in mice.
 We investigated the effects of R-flurbiprofen on cell proliferation and apoptosis in pituitary adenoma cell lines. GH4C1 rat
 pituitary cell line cultures and low-passage human primary pituitary cell cultures were treated with varying concentrations
 of R-flurbiprofen (0.1–1.0&amp;nbsp;mM). R-flurbiprofen inhibited cell proliferation in a dose-dependent fashion. A terminal deoxynucleotidyl
 transferase dUTP nick end labeling assay and chromatin condensation/dead cell apoptosis assay demonstrated induction of apoptosis
 at higher concentrations of R-flurbiprofen. R-flurbiprofen decreases cell proliferation and induces apoptosis in pituitary
 adeno...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5260143</comments>
            <pubDate>Thu, 22 Sep 2011 06:37:28 +0100</pubDate>
            <guid isPermaLink="false">5260143</guid>        </item>
        <item>
            <title>mRNA stability alterations mediated by HuR are necessary to sustain the fast growth of glioma cells</title>
            <link>http://www.medworm.com/index.php?rid=5260145&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fdh0j8k262214p501%2F</link>
            <description>In conclusion,
 our data suggest that post-transcriptional control abnormalities mediated by HuR are necessary to sustain the rapid growth
 of this devastating type of cancer.
 
 
	Content Type Journal ArticleCategory Laboratory Investigation - Human/Animal TissuePages 1-12DOI 10.1007/s11060-011-0707-1Authors
		Federico Bolognani, Department of Neurosurgery, The Methodist Hospital and The Methodist Hospital Research Institute, 6560 Fannin Street, Scurlock Tower Suite 944, Houston, TX 77030, USAAnne-Isabelle Gallani, Novartis Institutes for Biomedical Research, Novartis Pharma AG, Basel, SwitzerlandLena Sokol, Novartis Institutes for Biomedical Research, Novartis Pharma AG, Basel, SwitzerlandDavid S. Baskin, Department of Neurosurgery, The Methodist Hospital and The Methodist Hospital Resea...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5260145</comments>
            <pubDate>Wed, 21 Sep 2011 05:47:51 +0100</pubDate>
            <guid isPermaLink="false">5260145</guid>        </item>
        <item>
            <title>Isolation of a new cell population in the glioblastoma microenvironment</title>
            <link>http://www.medworm.com/index.php?rid=5236793&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fpt6316nk3k1641r2%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Glioblastoma (GB) is a highly infiltrative tumor recurring in 90% of cases within a few centimeters of the resection cavity,
 even in cases of complete tumor resection and adjuvant chemo/radiotherapy. This observation highlights the importance of understanding
 this special zone of brain tissue surrounding the tumor. It is becoming clear that the nonneoplastic stromal compartment of
 most solid cancers plays an active role in tumor proliferation, invasion, and metastasis. Very little information, other than
 that concerning angiogenesis and immune cells, has been collected for stromal cells from GB. As part of a translational research
 program, we have isolated a new stromal cell population surrounding GB by computer-guided stereotaxic biopsies and primary
 culture. We ...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5236793</comments>
            <pubDate>Sat, 17 Sep 2011 17:07:11 +0100</pubDate>
            <guid isPermaLink="false">5236793</guid>        </item>
        <item>
            <title>Knockdown of cyclin D1 inhibits proliferation, induces apoptosis, and attenuates the invasive capacity of human glioblastoma cells</title>
            <link>http://www.medworm.com/index.php?rid=5224736&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fn541n3vxh4x5n404%2F</link>
            <description>In this study, the human glioblastoma
 cell lines SHG-44 and U251 were stably transfected with short hairpin RNA (shRNA) targeting cyclin&amp;nbsp;D1 or with ectogenic cyclin&amp;nbsp;D1
 by lentivirus-mediated transfection. Glioblastoma cells overexpressing or underexpressing cyclin&amp;nbsp;D1 were then examined by
 in&amp;nbsp;vitro growth assays, apoptosis assays, cell cycle analysis, and invasion assays. Cyclin&amp;nbsp;D1 knockdown in SHG-44 cells inhibited
 cell proliferation, induced apoptosis, and attenuated migration across Matrigel, a model of invasive capacity. Western blot
 analysis and quantitative reverse-transcription polymerase chain reaction (RT-PCR) revealed that cells underexpressing CCND1
 exhibited decreased multidrug resistance protein&amp;nbsp;1 (MDR1) and B-cell lymphoma-2 (Bcl-2) express...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5224736</comments>
            <pubDate>Tue, 13 Sep 2011 05:50:21 +0100</pubDate>
            <guid isPermaLink="false">5224736</guid>        </item>
        <item>
            <title>Regulation of histone acetylation by NDRG2 in glioma cells</title>
            <link>http://www.medworm.com/index.php?rid=5224737&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F5236022k06117571%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;
 NDRG2, a member of the N-Myc downstream-regulated gene family, was shown to be a putative tumor suppressor gene in glioblastoma
 and other cancers. Through a bioinformatic analysis, we found that NDRG2 protein contains an acyl carrier domain. In the current
 study, we therefore hypothesized that NDRG2 may play an important role in the regulation of histone acetylation. Treatment
 of U251 and U87 glioma cells with trichostatin A, an inhibitor of histone deacetylase, upregulated the expression of NDRG2
 and acetylated forms of histones H3 and H4, reduced tumor cell viability and arrested the cell cycle at the G1/G0 phase.
 Overexpression of NDRG2 by transfecting glioma cells with adenovirus containing the NDRG2 gene upregulated the levels of acetylated forms of H3 and H...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5224737</comments>
            <pubDate>Tue, 13 Sep 2011 05:50:20 +0100</pubDate>
            <guid isPermaLink="false">5224737</guid>        </item>
        <item>
            <title>Glioma residual or recurrence versus radiation necrosis: accuracy of pentavalent technetium-99m-dimercaptosuccinic acid [Tc-99m (V) DMSA] brain SPECT compared to proton magnetic resonance spectroscopy (1H-MRS): initial results</title>
            <link>http://www.medworm.com/index.php?rid=5224738&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fwn460u45634286x8%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;We compared pentavalent technetium-99m dimercaptosuccinic acid (Tc-99m (V) DMSA) brain single photon emission computed tomography
 (SPECT) and proton magnetic resonance spectroscopy (1H-MRS) for the detection of residual or recurrent gliomas after surgery and radiotherapy. A total of 24 glioma patients, previously
 operated upon and treated with radiotherapy, were studied. SPECT was acquired 2–3&amp;nbsp;h post-administration of 555–740 MBq of
 Tc-99m (V) DMSA. Lesion to normal (L/N) delayed uptake ratio was calculated as: mean counts of tumor ROI (L)/mean counts of
 normal mirror symmetric ROI (N). 1H-MRS was performed using a 1.5-T scanner equipped with a spectroscopy package. SPECT and 1H-MRS results were compared with pathology or follow-up neuroimaging studies. SPE...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5224738</comments>
            <pubDate>Mon, 12 Sep 2011 15:53:30 +0100</pubDate>
            <guid isPermaLink="false">5224738</guid>        </item>
        <item>
            <title>Downregulation of KIF23 suppresses glioma proliferation</title>
            <link>http://www.medworm.com/index.php?rid=5207892&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fu1658445r264457p%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;To identify therapeutic molecular targets for glioma, we performed modified serological identification of antigens by recombinant
 complementary DNA (cDNA) expression cloning using sera from a mouse glioma model. Two clones, kinesin family member&amp;nbsp;23 (Kif23)
 and structural maintenance of chromosomes&amp;nbsp;4 (Smc4), were identified as antigens through immunological reaction with sera from
 mice harboring synergic GL261 mouse glioma and intratumoral inoculation with a mutant herpes simplex virus. The human Kif23
 homolog KIF23 is a nuclear protein that localizes to the interzone of mitotic spindles, acting as a plus-end-directed motor
 enzyme that moves antiparallel microtubules in&amp;nbsp;vitro. Expression analysis revealed a higher level of KIF23 expression in glioma
 ...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5207892</comments>
            <pubDate>Fri, 09 Sep 2011 06:00:04 +0100</pubDate>
            <guid isPermaLink="false">5207892</guid>        </item>
        <item>
            <title>Proceedings of the diffuse intrinsic pontine glioma (DIPG) Toronto Think Tank: advancing basic and translational research and cooperation in DIPG</title>
            <link>http://www.medworm.com/index.php?rid=5207893&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fm0r4t22185742707%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Diffuse intrinsic pontine glioma (DIPG) nearly exclusively affects children. The prognosis of DIPGs has remained grim despite
 more than three decades of clinical research and numerous clinical trials. More than 90% of the children with DIPG will succumb
 within 2&amp;nbsp;years of diagnosis. The tumor’s incidence is still undefined, but data suggest 100–150 affected children annually
 in the US. The single proven effective treatment modality in DIPG remains radiation therapy. For the majority of patients
 however this treatment is only of transient effectiveness. Recent breakthroughs in the understanding of the molecular biology
 of DIPG have raised new hope and opened new avenues for therapeutic options. The advancement of basic and translational research
 and coopera...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5207893</comments>
            <pubDate>Thu, 08 Sep 2011 05:58:27 +0100</pubDate>
            <guid isPermaLink="false">5207893</guid>        </item>
        <item>
            <title>Erratum to: The role of radiotherapy in adult medulloblastoma: long-term single-institution experience and a review of the literature</title>
            <link>http://www.medworm.com/index.php?rid=5207894&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fx017373077mg2048%2F</link>
            <description>Content Type Journal ArticleCategory ErratumPages 1-1DOI 10.1007/s11060-011-0708-0Authors
		M. Balducci, Bio-Images and Radiological Sciences Department, Radiotherapy Institute, Catholic University of Rome, 00168 Rome, ItalyS. Chiesa, Bio-Images and Radiological Sciences Department, Radiotherapy Institute, Catholic University of Rome, 00168 Rome, ItalyD. Chieffo, Neurosurgery Institute, Catholic University of Rome, 00168 Rome, ItalyS. Manfrida, Bio-Images and Radiological Sciences Department, Radiotherapy Institute, Catholic University of Rome, 00168 Rome, ItalyN. Dinapoli, Bio-Images and Radiological Sciences Department, Radiotherapy Institute, Catholic University of Rome, 00168 Rome, ItalyA. Fiorentino, Bio-Images and Radiological Sciences Department, Radiotherapy Institute, Catholic U...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5207894</comments>
            <pubDate>Tue, 06 Sep 2011 15:49:34 +0100</pubDate>
            <guid isPermaLink="false">5207894</guid>        </item>
        <item>
            <title>Identification of CD105 (endoglin)-positive stem-like cells in rhabdoid meningioma</title>
            <link>http://www.medworm.com/index.php?rid=5207895&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F9838j775205w452q%2F</link>
            <description>In conclusion, a population of CD105-positive TICs with some traits of MPCs was identified in RM and might provide a promising
 therapeutic target in management of malignant meningioma.
 
 
	Content Type Journal ArticleCategory Laboratory Investigation - Human/Animal TissuePages 1-13DOI 10.1007/s11060-011-0705-3Authors
		Dezhi Hu, Department of Neurosurgery, Huashan Hospital, Fudan University, Shanghai, ChinaXiaomei Wang, Department of Neurology, The Tenth People’s Hospital, Tongji University, Shanghai, ChinaYing Mao, Department of Neurosurgery, Huashan Hospital, Fudan University, Shanghai, ChinaLiangfu Zhou, Department of Neurosurgery, Huashan Hospital, Fudan University, Shanghai, China
	

	
		Journal Journal of Neuro-OncologyOnline ISSN 1573-7373Print ISSN 0167-594X (Source: Journal of...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5207895</comments>
            <pubDate>Mon, 05 Sep 2011 16:14:38 +0100</pubDate>
            <guid isPermaLink="false">5207895</guid>        </item>
        <item>
            <title>Evidence for involvement of ROCK signaling in bradykinin-induced increase in murine blood–tumor barrier permeability</title>
            <link>http://www.medworm.com/index.php?rid=5207897&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fu8055228n92g7642%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;We have previously shown that activation of RhoA by bradykinin (BK) is associated with cytoskeleton rearrangement, tight junction
 (TJ) protein disassembly, and an increase in blood–tumor barrier (BTB) permeability in rat brain microvascular endothelial
 cells (RBMECs). Subsequently, we investigated whether Rho-kinases (ROCKs), a family of downstream effectors of activated RhoA
 known to stimulate F-actin rearrangement, play a key role in the above-mentioned processes in RBMECs. Our study uses primary
 RBMECs as an in&amp;nbsp;vitro BTB model and a specific ROCK inhibitor (Y-27632) and ROCK&amp;nbsp;II small interfering RNA (siRNA) to establish
 whether ROCK plays a role in the process of TJ opening by BK. Y-27632 and ROCK&amp;nbsp;II siRNA could partially inhibit endothelial
 le...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5207897</comments>
            <pubDate>Sun, 04 Sep 2011 10:45:39 +0100</pubDate>
            <guid isPermaLink="false">5207897</guid>        </item>
        <item>
            <title>Dosimetric comparison of Linac-based (BrainLAB®) and robotic radiosurgery (CyberKnife®) stereotactic system plans for acoustic schwannoma</title>
            <link>http://www.medworm.com/index.php?rid=5207896&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fl477788044620036%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;A dosimetric comparison of linear accelerator (LA)-based (BrainLAB) and robotic radiosurgery (RS) (CyberKnife) systems for
 acoustic schwannoma (Acoustic neuroma, AN) was carried out. Seven patients with radiologically confirmed unilateral AN were
 planned with both an LA-based (BrainLAB) and robotic RS (CyberKnife) system using the same computed tomography (CT) dataset
 and contours. Gross tumour volume (GTV) was contoured on post-contrast magnetic resonance imaging (MRI) scan [planning target
 volume (PTV) margin 2&amp;nbsp;mm]. Planning and calculation were done with appropriate calculation algorithms. The prescribed isodose
 in both systems was considered adequate to cover at least 95% of the contoured target. Plan evaluations were done by examining
 the target coverage...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5207896</comments>
            <pubDate>Sun, 04 Sep 2011 10:45:39 +0100</pubDate>
            <guid isPermaLink="false">5207896</guid>        </item>
        <item>
            <title>Patterns of care and survival for glioblastoma patients in the Veterans population</title>
            <link>http://www.medworm.com/index.php?rid=5183332&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fb641m682321l14u0%2F</link>
            <description>In conclusion,
 we found that more aggressive therapy was associated with better survival, even among elderly Veterans and whether compared
 overall or by age group, VA patients showed decreased survival relative to a national cohort. We believe this potential disparity
 warrants further investigation.
 
 
	Content Type Journal ArticleCategory Clinical Study – Patient StudyPages 1-9DOI 10.1007/s11060-011-0702-6Authors
		Robert T. Arrigo, Stanford University School of Medicine, 300 Pasteur Drive, Stanford, CA 94305, USAMaxwell Boakye, Outcomes Research Lab, VA Palo Alto Health Care System, 3801 Miranda Ave, Palo Alto, CA 94304, USAStephen L. Skirboll, Outcomes Research Lab, VA Palo Alto Health Care System, 3801 Miranda Ave, Palo Alto, CA 94304, USA
	

	
		Journal Journal of Neuro-Oncology...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5183332</comments>
            <pubDate>Wed, 31 Aug 2011 15:55:29 +0100</pubDate>
            <guid isPermaLink="false">5183332</guid>        </item>
        <item>
            <title>Cyberknife hypofractionated stereotactic radiosurgery (HSRS) of resection cavity after excision of large cerebral metastasis: efficacy and safety of an 800 cGy × 3 daily fractions regimen</title>
            <link>http://www.medworm.com/index.php?rid=5183333&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F045472457r44v32g%2F</link>
            <description>This study demonstrates the safety and efficacy of an 800&amp;nbsp;cGy&amp;nbsp;×&amp;nbsp;3 daily fractions CyberKnife® HSRS regimen for irradiation of large resection cavity. The efficacy compares favorably to historical data derived from patients
 undergoing WBRT, SRS, or brachytherapy.
 
 
	Content Type Journal ArticleCategory Clinical Study – Patient StudyPages 1-10DOI 10.1007/s11060-011-0697-zAuthors
		Che-Chuan Wang, Department of Neurosurgery, Chi Mei Medical Center, Tainan, TaiwanScott R. Floyd, Department of Radiation Oncology, Beth Israel Deaconess Medical Center, Boston, MA, USAChin-Hong Chang, Department of Neurosurgery, Chi Mei Medical Center, Tainan, TaiwanPeter C. Warnke, Division of Neurosurgery, University of Chicago Medical Center, Chicago, IL, USAChung-Ching Chio, Department of...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5183333</comments>
            <pubDate>Wed, 31 Aug 2011 05:52:39 +0100</pubDate>
            <guid isPermaLink="false">5183333</guid>        </item>
        <item>
            <title>Novel approaches to treating leptomeningeal metastases</title>
            <link>http://www.medworm.com/index.php?rid=5175465&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fy711p22448606055%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Leptomeningeal metastasis is a devastating complication of the central nervous system in patients with late-stage solid or
 hematological cancers. Leptomeningeal metastasis results from the multifocal seeding of the leptomeninges by malignant cancer
 cells. Although central nervous system metastasis usually presents in patients with widely disseminated and progressive late-stage
 cancer, malignant cells may spread to the cerebrospinal fluid during earlier disease stages in particularly aggressive cancers.
 Treatment of leptomeningeal metastasis is largely palliative but will often provide stabilization and protection from further
 neurological deterioration and improve quality of life. There is a need to raise awareness of the impact of leptomeningeal
 metastases on can...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5175465</comments>
            <pubDate>Sat, 27 Aug 2011 15:49:29 +0100</pubDate>
            <guid isPermaLink="false">5175465</guid>        </item>
        <item>
            <title>Adult medulloblastoma: multiagent chemotherapy with cisplatinum and etoposide: a single institutional experience</title>
            <link>http://www.medworm.com/index.php?rid=5175467&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F98l7078431854025%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;In 1991, a prospective phase II trial was initiated to evaluate the efficacy of treatment for adults with medulloblastoma
 (MB). After surgery, patients were staged with a neuroradiologic examination of the brain and neuroaxis and by cerebrospinal
 fluid cytology. All patients received three cycles of upfront cisplatinum (cisplatinum) and etoposide (VP16) chemotherapy
 followed by cranio-spinal radiation therapy. The current article reports on the long-term results from that trial. After a
 median follow-up of 14.9&amp;nbsp;years, among a total of 28 adults with MB, the overall progression-free survival and overall survival
 (OS) rates at 5&amp;nbsp;years were 57.6 and 80%, respectively. The median OS for the whole group of patients was 11.3&amp;nbsp;years. The observed
 toxicity w...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5175467</comments>
            <pubDate>Sat, 27 Aug 2011 05:57:11 +0100</pubDate>
            <guid isPermaLink="false">5175467</guid>        </item>
        <item>
            <title>Germinoma occurring 2 years after total resection of an intracranial epidermoid cyst in the pineal region</title>
            <link>http://www.medworm.com/index.php?rid=5175466&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F11167v60r167254g%2F</link>
            <description>Germinoma occurring 2 years after total resection of an intracranial epidermoid cyst in the pineal region
	Content Type Journal ArticleCategory Letter to the EditorPages 1-3DOI 10.1007/s11060-011-0683-5Authors
		Qing Mao, Department of Neurosurgery, West China Hospital, Sichuan University, Wai Nan Guo Xue Xiang 37, Chengdu, 610041 Sichuan, ChinaLu Ma, Department of Neurosurgery, West China Hospital, Sichuan University, Wai Nan Guo Xue Xiang 37, Chengdu, 610041 Sichuan, ChinaZhongguo Pang, Department of Pathology, West China Hospital, Sichuan University, Chengdu, Sichuan, ChinaJiagang Liu, Department of Neurosurgery, West China Hospital, Sichuan University, Wai Nan Guo Xue Xiang 37, Chengdu, 610041 Sichuan, China
	

	
		Journal Journal of Neuro-OncologyOnline ISSN 1573-7373Print ISSN 0167-...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5175466</comments>
            <pubDate>Sat, 27 Aug 2011 05:57:11 +0100</pubDate>
            <guid isPermaLink="false">5175466</guid>        </item>
        <item>
            <title>A phase II trial of thalidomide and procarbazine in adult patients with recurrent or progressive malignant gliomas</title>
            <link>http://www.medworm.com/index.php?rid=5175468&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fcrn5h70821u10407%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Thalidomide and procarbazine have demonstrated single agent activity against malignant gliomas (MG). We evaluated the combination
 of thalidomide and procarbazine with a single arm phase II trial in adults with recurrent or progressive MG. Procarbazine
 was given at a dose of 250&amp;nbsp;mg/m2/d&amp;nbsp;×&amp;nbsp;5day q 28&amp;nbsp;days. Thalidomide was administered at a dose of 200&amp;nbsp;mg/day continuously. Intrapatient dose escalation of thalidomide
 was attempted (increase by 100&amp;nbsp;mg/day weekly as tolerated) to a maximum of 800&amp;nbsp;mg/day. The primary outcome was tumor response,
 assessed by MRI and CT. Secondary outcomes were progression free survival (PFS), overall survival (OS) and toxicity. In addition,
 quality of life questionnaires were performed at baseline and prio...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5175468</comments>
            <pubDate>Thu, 25 Aug 2011 15:51:25 +0100</pubDate>
            <guid isPermaLink="false">5175468</guid>        </item>
        <item>
            <title>Pediatric infratentorial ependymoma: prognostic significance of anaplastic histology</title>
            <link>http://www.medworm.com/index.php?rid=5161011&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fy7h2823lj34387l8%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Pediatric infratentorial ependymomas are difficult to cure. Despite the availability of advanced therapeutic modalities for
 brain tumors, total surgical resection remains the most important prognostic factor. Recently, histological grade emerged
 as an independent prognostic factor for intracranial ependymoma. We retrospectively reviewed the treatment outcome of 33 pediatric
 patients with infratentorial ependymoma. Progression-free survival (PFS) and overall survival (OS) rates were calculated and
 relevant prognostic factors were analyzed. Fourteen patients (42%) were under the age of 3 at diagnosis. Gross total resection
 was achieved in 16 patients (49%). Anaplastic histology was found in 13 patients (39%). Adjuvant therapies were delayed until
 progression in 12 p...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5161011</comments>
            <pubDate>Wed, 24 Aug 2011 05:55:38 +0100</pubDate>
            <guid isPermaLink="false">5161011</guid>        </item>
        <item>
            <title>HESRG: a novel biomarker for intracranial germinoma and embryonal carcinoma</title>
            <link>http://www.medworm.com/index.php?rid=5161013&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F1016r400178v0070%2F</link>
            <description>In this study, we used RT-PCR to systematically investigate the expression of HESRG in various types of intracranial
 tumors and found that HESRG was expressed only in germinoma and embryonal carcinoma, but hardly at all in other types of
 brain tumors. Real-time PCR results further confirmed this expression pattern. Subsequently, we tested 134 intracranial non-germ
 cell tumors and 64 intracranial germ cell tumors by immunohistochemistry. Our results showed that HESRG was expressed strongly
 and diffusively in the nuclei of tumor cells in intracranial germinoma and embryonal carcinoma as well as in human embryonic
 stem cells. No positive staining signal was observed in any other type of intracranial tumors. In germinomas, 25 of 31 showed
 intensive (3+) expression, four cases showed mode...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5161013</comments>
            <pubDate>Tue, 23 Aug 2011 05:54:48 +0100</pubDate>
            <guid isPermaLink="false">5161013</guid>        </item>
        <item>
            <title>Single and hypofractionated stereotactic radiotherapy with CyberKnife for craniopharyngioma</title>
            <link>http://www.medworm.com/index.php?rid=5161012&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Frw1w24q85r779723%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Craniopharyngiomas are slow-growing tumors found in the suprasellar region, with especially high incidence in Japanese children.
 Due to the location, proximity and adhesiveness of the tumor to adjacent critical structures, these tumors remain a significant
 clinical challenge. The purpose of this study was to evaluate the clinical outcome of single and hypofractionated stereotactic
 radiotherapy (SRT) with CyberKnife for craniopharyngioma. Forty-three patients (21 men and 22 women; median age 44&amp;nbsp;years;
 range 3–85&amp;nbsp;years) were treated at two institutions. Three cases were treated in a single fraction to a marginal dose of 13–16&amp;nbsp;Gy.
 The other 40 cases were treated in 2–5 fractions to a marginal dose of 13–25&amp;nbsp;Gy. Tumor volumes ranged from 0.09...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5161012</comments>
            <pubDate>Tue, 23 Aug 2011 05:54:48 +0100</pubDate>
            <guid isPermaLink="false">5161012</guid>        </item>
        <item>
            <title>Matrix metalloproteinase-1 expression enhances tumorigenicity as well as tumor-related angiogenesis and is inversely associated with TIMP-4 expression in a model of glioblastoma</title>
            <link>http://www.medworm.com/index.php?rid=5161014&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F5846742542375k26%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Herein we continue the study of matrix metalloproteinase-1 (MMP-1) with respect to glioblastoma multiforme (GBM) cell tumorigenicity
 and angiogenesis. A model of tumorigenicity with cells stably altered to over-express or knock-down MMP-1 revealed that it
 significantly increases tumor incidence and size. Organized endothelial growth in human umbilical vein endothelial cell (HUVEC)-GBM
 co-cultures was significantly increased in the presence of MMP-1. CD31 analysis of model tumors elucidated a substantial recruitment
 of endothelium in MMP-1 enhanced samples. Antibody arrays indicated an inverse expression of certain anti-angiogenic factors
 with respect to MMP-1, the most notable of which was a significant increase in tissue inhibitor of metalloproteinases-4 (TIMP-4)
...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5161014</comments>
            <pubDate>Sat, 20 Aug 2011 15:52:31 +0100</pubDate>
            <guid isPermaLink="false">5161014</guid>        </item>
        <item>
            <title>Radiotherapy with concurrent and adjuvant temozolomide in children with newly diagnosed diffuse intrinsic pontine glioma</title>
            <link>http://www.medworm.com/index.php?rid=5161015&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fu113722615m650u3%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The purpose of this study is to evaluate the efficacy and toxicity of radiation therapy (RT) with concurrent temozolomide
 (TMZ) chemotherapy followed by adjuvant TMZ in children with diffuse intrinsic pontine glioma (DIPG). Newly diagnosed patients
 younger than 18&amp;nbsp;years with histologically proven DIPG were treated with focal radiotherapy to a dose of 54&amp;nbsp;Gy in 30 fractions
 along with concurrent daily TMZ (75&amp;nbsp;mg/m2/day). Four weeks after completing the initial RT–TMZ schedule, adjuvant TMZ (200&amp;nbsp;mg/m2/day, days 1–5) was given every 28&amp;nbsp;days up to six cycles. Responses/progressions were assessed by clinical and 2-monthly MRI
 follow-up studies. Between September 2005 and September 2009, 21 patients with newly diagnosed histologically confirmed...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5161015</comments>
            <pubDate>Sat, 20 Aug 2011 05:42:27 +0100</pubDate>
            <guid isPermaLink="false">5161015</guid>        </item>
        <item>
            <title>Treatment of recurrent diffuse intrinsic pontine glioma: the MD Anderson Cancer Center experience</title>
            <link>http://www.medworm.com/index.php?rid=5161016&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fk3054t0xp0j117r2%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Recurrent diffuse intrinsic pontine gliomas (DIPG) are traditionally treated with palliative care since no effective treatments
 have been described for these tumors. Recently, clinical studies have been emerging, and individualized treatment is attempted
 more frequently. However, an informative way to compare the treatment outcomes has not been established, and historical control
 data are missing for recurrent disease. We conducted a retrospective chart review of patients with recurrent DIPG treated
 between 1998 and 2010. Response progression-free survival and possible influencing factors were evaluated. Thirty-one patients
 were identified who were treated in 61 treatment attempts using 26 treatment elements in 31 different regimens. The most frequently
 used drugs...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5161016</comments>
            <pubDate>Sat, 20 Aug 2011 05:42:26 +0100</pubDate>
            <guid isPermaLink="false">5161016</guid>        </item>
        <item>
            <title>Cell phones and glioma risk: a review of the evidence</title>
            <link>http://www.medworm.com/index.php?rid=5161018&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fp576807187145406%2F</link>
            <description>Content Type Journal ArticleCategory Topic ReviewPages 1-13DOI 10.1007/s11060-011-0663-9Authors
		Courtney Corle, Department of Neurosciences, UC San Diego, Moores UCSD Cancer Center, 3855 Health Sciences Drive, MC 0819, La Jolla, CA 92093-0819, USAMilan Makale, Department of Neurosciences, UC San Diego, Moores UCSD Cancer Center, 3855 Health Sciences Drive, MC 0819, La Jolla, CA 92093-0819, USASantosh Kesari, Department of Neurosciences, UC San Diego, Moores UCSD Cancer Center, 3855 Health Sciences Drive, MC 0819, La Jolla, CA 92093-0819, USA
	

	
		Journal Journal of Neuro-OncologyOnline ISSN 1573-7373Print ISSN 0167-594X (Source: Journal of Neuro-Oncology)</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5161018</comments>
            <pubDate>Fri, 19 Aug 2011 05:49:36 +0100</pubDate>
            <guid isPermaLink="false">5161018</guid>        </item>
        <item>
            <title>Incidental brain lesions in children: to treat or not to treat?</title>
            <link>http://www.medworm.com/index.php?rid=5161017&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fp765745108600k23%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Central nervous system (CNS) lesions that are discovered incidentally when imaging children for problems that were unrelated
 to the detected lesion pose a dilemma to physicians. Because there are few data on the outcome of such cases, we retrospectively
 reviewed the clinical course of a group of children followed at our institution with brain lesions found incidentally on neuro-imaging.
 A database of all children with brain lesions followed at the University of Rochester medical center from 2000 to 2010 was
 reviewed. Data were obtained regarding presentation, magnetic resonance imaging (MRI) features, treatment, progression-free
 survival, and overall survival of children with brain lesions found incidentally. Of the 244 children with brain lesions seen
 over this t...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5161017</comments>
            <pubDate>Fri, 19 Aug 2011 05:49:36 +0100</pubDate>
            <guid isPermaLink="false">5161017</guid>        </item>
        <item>
            <title>Is there a role for high dose chemotherapy with hematopoietic stem cell rescue in patients with relapsed supratentorial PNET?</title>
            <link>http://www.medworm.com/index.php?rid=5161020&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fc67n56858703wg51%2F</link>
            <description>In conclusion
 high dose chemotherapy with HSCR might lead to survival primarily in younger children with relapsed sPNET even in the absence
 of concomitant use of radiotherapy, whereas the outcome in older children and/or in pineal location is extremely poor with
 this modality.
 
 
	Content Type Journal ArticleCategory Topic ReviewPages 1-7DOI 10.1007/s11060-011-0690-6Authors
		C. P. Raghuram, Children and Young People’s Unit, The Royal Marsden NHS Foundation Trust, Downs Road, Sutton, SM2 5PT UKL. Moreno, Children and Young People’s Unit, The Royal Marsden NHS Foundation Trust, Downs Road, Sutton, SM2 5PT UKS. Zacharoulis, Children and Young People’s Unit, The Royal Marsden NHS Foundation Trust, Downs Road, Sutton, SM2 5PT UK
	

	
		Journal Journal of Neuro-OncologyOnline ISSN 157...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5161020</comments>
            <pubDate>Thu, 18 Aug 2011 05:50:00 +0100</pubDate>
            <guid isPermaLink="false">5161020</guid>        </item>
        <item>
            <title>Expression profile of frizzled receptors in human medulloblastomas</title>
            <link>http://www.medworm.com/index.php?rid=5161019&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Flu0186w594311g71%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Secreted WNT proteins signal through ten receptors of the frizzled (FZD) family. Because of the relevance of the WNT/β-catenin
 (CTNNB1) signaling pathway in medulloblastomas (MBs), we investigated the expression of all ten members of the FZD gene family (FZD1-10) in 17 human MBs, four MB cell lines and in normal human cerebellum, using real-time PCR. We found that
 FZD2 transcript was over-expressed in all MBs and MB cell lines. Western blot analysis confirmed the expression of FZD2 at the
 protein level. Moreover, the levels of FZD2 transcript were found to correlate with those of ASPM transcript, a marker of mitosis essential for mitotic spindle function. Accordingly, ASPM mRNA was expressed at a very low level in the adult, post-mitotic, human cerebellum, at higher...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5161019</comments>
            <pubDate>Thu, 18 Aug 2011 05:50:00 +0100</pubDate>
            <guid isPermaLink="false">5161019</guid>        </item>
        <item>
            <title>Imaging 18F-fluorodeoxy glucose/11C-methionine uptake decoupling for identification of tumor cell infiltration in peritumoral brain edema</title>
            <link>http://www.medworm.com/index.php?rid=5161022&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Feq1040v11q379552%2F</link>
            <description>This study challenged this issue by performing voxel-wise analysis of 18F-fluorodeoxy glucose (FDG) and 11C-methionine positron emission tomography (PET) in peritumoral brain edemas. The authors studied ten malignant glioma and
 nine meningioma patients with peritumoral brain edema. A voxel-wise analysis of FDG and 11C-methionine PET was performed in order to quantify the correlation between uptake of these tracers in normal brain tissue
 and peritumoral brain edema. Decoupling score of the uptake of two tracers was calculated as the z-score from the estimated correlation between uptake of the two tracers in normal brain tissue. The decoupling score was also
 converted into images for visual inspection. Average decoupling score in the peritumoral brain edema was calculated and compared
 be...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5161022</comments>
            <pubDate>Wed, 17 Aug 2011 05:53:27 +0100</pubDate>
            <guid isPermaLink="false">5161022</guid>        </item>
        <item>
            <title>The nonsteroidal anti-inflammatory drug celecoxib suppresses the growth and induces apoptosis of human glioblastoma cells via the NF-κB pathway</title>
            <link>http://www.medworm.com/index.php?rid=5161021&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fn10254786k111438%2F</link>
            <description>This study provides evidence that celecoxib suppresses
 the growth of GBM cell lines partly by inhibiting the NF-κB signaling pathway.
 
 
	Content Type Journal ArticleCategory Laboratory Investigation - Human/Animal TissuePages 1-11DOI 10.1007/s11060-011-0662-xAuthors
		Gangadhara Reddy Sareddy, Department of Biotechnology, School of Life Sciences, University of Hyderabad, Hyderabad, 500046 IndiaKhamushavalli Geeviman, Department of Biotechnology, School of Life Sciences, University of Hyderabad, Hyderabad, 500046 IndiaChinta Ramulu, Department of Biotechnology, School of Life Sciences, University of Hyderabad, Hyderabad, 500046 IndiaPhanithi Prakash Babu, Department of Biotechnology, School of Life Sciences, University of Hyderabad, Hyderabad, 500046 India
	

	
		Journal Journal of Neur...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5161021</comments>
            <pubDate>Wed, 17 Aug 2011 05:53:27 +0100</pubDate>
            <guid isPermaLink="false">5161021</guid>        </item>
        <item>
            <title>Oxcarbazepine monotherapy in patients with brain tumor-related epilepsy: open-label pilot study for assessing the efficacy, tolerability and impact on quality of life</title>
            <link>http://www.medworm.com/index.php?rid=5161023&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fwnr671mv1837v751%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;We conducted a prospective, observational study to verify the efficacy, tolerability and impact on quality of life, mood and
 global neurocognitive performances of oxcarbazepine monotherapy in patients with brain tumor-related epilepsy (BTRE). Patients
 were followed for 12&amp;nbsp;months. We recruited 25 patients (11 females 14 males; mean age 49.7) affected with BTRE (17 de novo
 patients and 7 in monotherapy with other antiepileptics) and introduced oxcarbazepine monotherapy because of uncontrolled
 seizures and/or side effects. At first visit, patients underwent neurological examination, Qolie 31P V2, EORTC QLQC30, Zung
 self-depression rating scale (ZSDRS) and adverse events profile. A seizure diary was given to each patient. Follow-up duration
 was 1–12&amp;nbsp;months...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5161023</comments>
            <pubDate>Wed, 17 Aug 2011 05:53:26 +0100</pubDate>
            <guid isPermaLink="false">5161023</guid>        </item>
        <item>
            <title>Efficacy of interstitial continuous vincristine infusion in a bioluminescent rodent intracranial tumor model</title>
            <link>http://www.medworm.com/index.php?rid=5143180&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fm84p110822457903%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Interstitial chemotherapeutic drug infusion can bypass the blood–brain barrier, and provide high regional drug concentrations
 without systemic exposure. However, toxicity and efficacy for drugs administered via interstitial continuous (i.c.) infusion
 have not been characterized. In the current study, vincristine (VIN) was infused into the right frontal lobes of healthy Fisher
 344 rats at 30, 45, 60, and 120&amp;nbsp;μg/ml over a period of 7&amp;nbsp;days at 1&amp;nbsp;μl/h, using an Alzet osmotic pump to evaluate toxicity.
 C6 rat glioblastoma cells transduced with a luciferase gene were inoculated into the right frontal lobe of a second group
 of rats. VIN was administered to tumor bearing rats via i.c. infusion 7&amp;nbsp;days later and tumor growth was monitored by biolumines...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5143180</comments>
            <pubDate>Sun, 14 Aug 2011 05:45:40 +0100</pubDate>
            <guid isPermaLink="false">5143180</guid>        </item>
        <item>
            <title>Oligodendrogliomas in children</title>
            <link>http://www.medworm.com/index.php?rid=5131699&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ff6v613xt15932564%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Oligodendrogliomas are rare central nervous system (CNS) tumors in children. The purpose of this study was to identify prognostic
 factors for progression free survival (PFS) and overall survival (OS) in pediatric patients with oligodendrogliomas. We retrospectively
 analyzed clinical data on 37 pediatric patients with oligodendroglial tumors treated at Washington University. Kaplan–Meier
 method was used to calculate survival rates. Log-rank was used to detect the difference between survival curves. The median
 age was 11.1&amp;nbsp;years (range 10&amp;nbsp;months–18&amp;nbsp;years), and median follow-up was 4.5&amp;nbsp;years (range 2&amp;nbsp;months–30.5&amp;nbsp;years). The 5-year
 PFS and OS were 66.4 and 93.4%, respectively. Mixed histology was associated with worse OS compared to ...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5131699</comments>
            <pubDate>Sat, 13 Aug 2011 06:13:11 +0100</pubDate>
            <guid isPermaLink="false">5131699</guid>        </item>
        <item>
            <title>MicroRNAs involved in the EGFR/PTEN/AKT pathway in gliomas</title>
            <link>http://www.medworm.com/index.php?rid=5131698&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F064048224142t82l%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Gliomas are the most common type of malignant primary brain tumor. Despite advances in surgery, radiation therapy, and chemotherapy,
 the prognosis of patients with gliomas has not significantly improved. MicroRNAs (miRNAs), a class of non-coding RNAs, 21–25
 nucleotides long, negatively regulate the expression of target genes by interacting with specific sites in mRNAs, and play
 a critical role in the development of gliomas. The EGFR/PTEN/AKT pathway is a promising target for anti-glioma therapy. Recent
 studies have showed that regulation of the EGFR/PTEN/AKT pathway by miRNAs plays a major role in glioma progression, indicating
 a novel way to investigate the tumorigenesis, diagnosis, and therapy of gliomas. Here, we focus on recent findings of miRNAs
 with respec...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5131698</comments>
            <pubDate>Sat, 13 Aug 2011 06:13:11 +0100</pubDate>
            <guid isPermaLink="false">5131698</guid>        </item>
        <item>
            <title>Modulation of pediatric brain tumor autophagy and chemosensitivity</title>
            <link>http://www.medworm.com/index.php?rid=5131697&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F8484134352x82648%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Brain and spinal tumors are the second most common malignancies in childhood after leukemia, and they remain the leading cause
 of death from childhood cancer. Autophagy is a catabolic cellular process that is thought to regulate chemosensitivity, however
 its role in pediatric tumors is unknown. Here we present studies in pediatric medulloblastoma cell lines (DAOY, ONS76) and
 atypical teratoid/rhabdoid tumor cell lines (BT-16, BT-12) to test this role. Autophagy was inhibited using siRNA against
 autophagy-related genes ATG12 and ATG7 or pharmacologically induced or inhibited using rapamycin and chloroquine to test the
 effect of autophagy on chemosensitivity. Autophagic flux was measured using Western blot analysis of LC3-II and p62 and cell
 viability was determined...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5131697</comments>
            <pubDate>Sat, 13 Aug 2011 06:13:11 +0100</pubDate>
            <guid isPermaLink="false">5131697</guid>        </item>
        <item>
            <title>Subcutaneous tumor seeding after biopsy in gliomatosis cerebri</title>
            <link>http://www.medworm.com/index.php?rid=5131700&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fd11w7105n8281351%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;We observed a patient with subcutaneous seeding from gliomatosis cerebri with a low-grade histopathology. A 33-year-old woman
 with neurofibromatosis type 1 presented with progressive headache, diplopia, dysphagia, and a rightward instability. On neurological
 examination dysarthria, gait ataxia, and left-sided central facial and hypoglossal palsies were determined. MRI of the brain
 demonstrated diffuse, infiltrative non-enhancing lesions in the pons, both cerebellar hemispheres, the parahippocampal gyrus,
 and the thalamus. A stereotactic biopsy demonstrated an astrocytoma WHO grade 2. These characteristics confirmed gliomatosis
 cerebri. Three months later, the patient presented with hydrocephalus and a subcutaneous swelling directly underneath the
 surgical scar. Th...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5131700</comments>
            <pubDate>Fri, 12 Aug 2011 06:18:36 +0100</pubDate>
            <guid isPermaLink="false">5131700</guid>        </item>
        <item>
            <title>Eltrombopag for radiation-induced thrombocytopenia in a glioblastoma patient</title>
            <link>http://www.medworm.com/index.php?rid=5131701&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F4370352307475j4l%2F</link>
            <description>Content Type Journal ArticlePages 1-3DOI 10.1007/s11060-011-0675-5Authors
		J. Paul Duic, Long Island Brain Tumor Center at Neurological Surgery, P.C. 600 Northern Blvd Suite 113, Great Neck, NY 11021, USAJai Grewal, Long Island Brain Tumor Center at Neurological Surgery, P.C. 600 Northern Blvd Suite 113, Great Neck, NY 11021, USAKerry McConie, Long Island Brain Tumor Center at Neurological Surgery, P.C. 600 Northern Blvd Suite 113, Great Neck, NY 11021, USAHarry Staszewski, Division of Hematology-Oncology, Winthrop University Hospital, Mineola, NY 11501, USAJonathan Haas, Department of Radiation Oncology, Winthrop University Hospital, Mineola, NY 11501, USASantosh Kesari, Department of Neurosciences, Moores Cancer Center, University of California, San Diego, 3855 Health Sciences Drive, ...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5131701</comments>
            <pubDate>Thu, 11 Aug 2011 06:03:16 +0100</pubDate>
            <guid isPermaLink="false">5131701</guid>        </item>
        <item>
            <title>Type 2 diabetes mellitus and obesity are independent risk factors for poor outcome in patients with high-grade glioma</title>
            <link>http://www.medworm.com/index.php?rid=5131702&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fb1m834266566l7tl%2F</link>
            <description>In this study we asked if type 2 DM and elevated body mass index (BMI)
 are independent risk factors for poor prognosis in patients with high-grade glioma (HGG.). We conducted a retrospective cohort
 study of 171 patients surgically treated for HGG at a single institution. BMI and records of pre-existing type 2 DM were obtained
 from medical histories. Variables associated with survival in a univariate analysis were included in the multivariate Cox
 model if P&amp;nbsp;&amp;lt;&amp;nbsp;0.10. Variables with probability values&amp;nbsp;&amp;gt;0.05 were then removed from the multivariate model in a step-wise fashion. Mean
 age at diagnosis was 55.0&amp;nbsp;±&amp;nbsp;17.3&amp;nbsp;years. Fifteen (8.8%) patients had a history of type 2 DM. Fifty-eight (35.8%) patients had
 a BMI&amp;nbsp;&amp;lt;&amp;nbsp;25, 55 (34.0%) BMI 25–30,...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5131702</comments>
            <pubDate>Thu, 11 Aug 2011 06:03:15 +0100</pubDate>
            <guid isPermaLink="false">5131702</guid>        </item>
        <item>
            <title>Pediatric intracranial ependymoma: the roles of surgery, radiation and chemotherapy</title>
            <link>http://www.medworm.com/index.php?rid=5126097&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F982046704172qw1h%2F</link>
            <description>In conclusion, for localized intracranial pediatric ependymomas, adjuvant
 RT is associated with improved PFS, even after adjusting for EOR. Our findings suggest the benefit of RT even in the presence
 of GTR. Future prospective studies with larger sample number are needed to validate our findings.
 
 
	Content Type Journal ArticlePages 1-9DOI 10.1007/s11060-011-0671-9Authors
		Sunanda Pejavar, Departments of Radiation Oncology, Neurosurgery, and Pediatrics, University of California, San Francisco and UCSF Benioff Children’s Hospital, 1600 Divisadero Street, Suite H1031, San Francisco, CA 94115-1708, USAMei-Yin Polley, Departments of Radiation Oncology, Neurosurgery, and Pediatrics, University of California, San Francisco and UCSF Benioff Children’s Hospital, 1600 Divisadero Street, Su...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5126097</comments>
            <pubDate>Tue, 09 Aug 2011 05:43:43 +0100</pubDate>
            <guid isPermaLink="false">5126097</guid>        </item>
        <item>
            <title>Gemcitabine induced myositis in patients with pancreatic cancer: case reports and topic review</title>
            <link>http://www.medworm.com/index.php?rid=5103734&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F4t48544g501w7736%2F</link>
            <description>We report two cases of gemcitabine related myositis identified at
 our institution, and perform a literature review of cases which meet the criteria for gemcitabine induced myositis associated
 to either radiation therapy or chemotherapy alone.
 
 
	Content Type Journal ArticlePages 1-7DOI 10.1007/s11060-011-0672-8Authors
		Elena Pentsova, Department of Neurology, Memorial Sloan-Kettering Cancer Center, 1275 York Avenue, New York, NY 10065, USAAnli Liu, Department of Neurology and Neuroscience, Weill Cornell College of Medicine of Cornell University, New York, NY, USAMarc Rosenblum, Department of Pathology, Memorial Sloan-Kettering Cancer Center, New York, NY 10065, USAEileen O’Reilly, Department of Medicine, Memorial Sloan-Kettering Cancer Center, New York, NY 10065, USAXi Chen, Departm...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5103734</comments>
            <pubDate>Wed, 03 Aug 2011 05:44:43 +0100</pubDate>
            <guid isPermaLink="false">5103734</guid>        </item>
        <item>
            <title>A clinicopathological study of diagnostically challenging meningioma mimics</title>
            <link>http://www.medworm.com/index.php?rid=5103733&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fc6p3w0g488622382%2F</link>
            <description>This study included
 total of 20 cases of meningioma mimics. The clinical, radiological and histopathological findings were evaluated. Tissue fixed
 in 10% formalin was routinely processed and 5&amp;nbsp;μ thick sections were cut and stained with hematoxylin &amp; eosin. Histochemistry
 and immunohistochemistry using avidin–biotin complex immunoperoxidase method was done wherever indicated. In the present study
 group, 15 were male and 5 female with a male: female ratio of 3:1. The age ranged from 14 to 78&amp;nbsp;years. Radiologically all
 these lesions were extra-axial in location, predominantly hypointense on T2W, isointense on T1W images and showed intense
 homogenous enhancement on contrast administration. Four cases were in pediatric age group with histopathological diagnosis
 of Rosai Dorfm...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5103733</comments>
            <pubDate>Wed, 03 Aug 2011 05:44:43 +0100</pubDate>
            <guid isPermaLink="false">5103733</guid>        </item>
        <item>
            <title>The role of radiotherapy in adult medulloblastoma: long-term single-institution experience and a review of the literature</title>
            <link>http://www.medworm.com/index.php?rid=5087229&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fm132l3x775008p1k%2F</link>
            <description>We report our long-term,
 single-institution experience of adult MB and a review of the literature. We analysed adult patients with histologically proved
 MB treated by postoperative radiotherapy. Primary endpoints were local control (LC), disease-free survival (DFS), and overall
 survival (OS). Acute toxicity was reported according to CTC-NCI score vers. 3.0 and specific neuropsychological assessment
 analysis was performed to define late brain toxicity. From 1990–2008, 13 patients were treated by craniospinal (CSI, 12/13)
 or cranial irradiation (1/13, because of bad clinical conditions). Median follow up was 101&amp;nbsp;months (64–218). Complete radiological
 response was observed in 12/13 patients and a partial response in 1/13. Ten-year LC, OS, and DFS were 91, 76, and 84%, respectiv...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5087229</comments>
            <pubDate>Sat, 30 Jul 2011 15:52:26 +0100</pubDate>
            <guid isPermaLink="false">5087229</guid>        </item>
        <item>
            <title>p53 expression predicts dismal outcome for medulloblastoma patients with metastatic disease</title>
            <link>http://www.medworm.com/index.php?rid=5087230&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fdt51102g420526n0%2F</link>
            <description>In this study, 169 patients with metastatic MB registered
 in the multicentre HIT2000 trial of the German Society of Pediatric Oncology and Haematology (GPOH) have been investigated
 to determine the importance of p53 protein expression in predicting survival. At a median follow-up of 4.1 years, 159 patients
 with p53-negative tumours had significantly better four-year event-free survival (EFS) and progression-free survival (PFS)
 (56 ± 11, 59 ± 4%) than 10 patients with p53-positive tumours (40 ± 16, 40 ± 16%; P = 0.018 for EFS, P = 0.007 for PFS, respectively). Furthermore, four-year overall survival (OS) of children with p53-negative tumours was higher
 than for children with p53-positive tumours (72&amp;nbsp;±&amp;nbsp;4 vs. 35&amp;nbsp;±&amp;nbsp;18%, P&amp;nbsp;=&amp;nbsp;0.05). Three of the p53-posit...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5087230</comments>
            <pubDate>Wed, 27 Jul 2011 17:02:42 +0100</pubDate>
            <guid isPermaLink="false">5087230</guid>        </item>
        <item>
            <title>O6-methylguanine-DNA-methyltransferase promoter methylation assessment by microdissection-assisted methylation-specific PCR and high resolution melting analysis in patients with glioblastomas</title>
            <link>http://www.medworm.com/index.php?rid=5087231&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F41k8p0n441177w30%2F</link>
            <description>This study demonstrates that MGMT methylation
 is not restricted to glioblastoma cells. Additionally, methylation-specific HRM is a feasible approach that can be readily
 applied to the methylation analysis of MGMT. A further study will be needed to determine the dynamic change of MGMT methylation
 in the tumor environment.
 
 
	Content Type Journal ArticlePages 1-8DOI 10.1007/s11060-011-0668-4Authors
		Seung-Ho Yang, Department of Neurosurgery, St. Vincent’s Hospital, The Catholic University of Korea, Suwon, KoreaKeun Soo Lee, Department of Neurosurgery, Seoul St. Mary’s Hospital, The Catholic University of Korea, 505 Banpo-dong, Seocho-gu, Seoul, 137-701 KoreaHea Jung Yang, Institute of Medical Science, St. Vincent’s Hospital, The Catholic University of Korea, Suwon, KoreaByeong Hw...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5087231</comments>
            <pubDate>Wed, 27 Jul 2011 05:49:52 +0100</pubDate>
            <guid isPermaLink="false">5087231</guid>        </item>
        <item>
            <title>Platelet-derived growth factor receptor (PDGFR) expression in primary spinal cord gliomas</title>
            <link>http://www.medworm.com/index.php?rid=5087232&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fq175621465t8twq1%2F</link>
            <description>In this study we perform immunohistochemical analysis of PDGFRα expression in a series of 33 primary intramedullary
 spinal cord gliomas of different types and grades. PDGFRα was seen to be expressed in a significant subset of these tumors
 across all major glioma types including ependymoma, oligodendroglioma, pilocytic astrocytoma, astrocytoma, and glioblastoma.
 These results support the hypothesis that growth factor signaling through the PDGFR may be important for the development of
 at least a subset of human spinal cord gliomas. Further studies investigating the prognostic significance of PDGFR expression
 as well as the role of PDGF signaling on the development of intramedullary spinal cord gliomas are warranted.
 
 
	Content Type Journal ArticlePages 1-8DOI 10.1007/s11060-011-0666...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5087232</comments>
            <pubDate>Tue, 26 Jul 2011 05:48:24 +0100</pubDate>
            <guid isPermaLink="false">5087232</guid>        </item>
        <item>
            <title>The toxicity of intrathecal bevacizumab in a rabbit model of leptomeningeal carcinomatosis</title>
            <link>http://www.medworm.com/index.php?rid=5087233&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fg5212308l3018370%2F</link>
            <description>Conclusion: Intraventricular BCM can be administered to rabbits without clinical or pathologic neurotoxicity. Survival
 following one dose of BCM in rabbits with LC should be cautiously interpreted given uncertainties regarding the dose, schedule,
 and limited expected benefit of this non-rabbit antibody. This neurotoxicity study provides safety data to allow phase I/II
 studies in humans with treatment refractory LC.
 
 
	Content Type Journal ArticlePages 1-8DOI 10.1007/s11060-011-0655-9Authors
		Priscilla K. Brastianos, Department of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, 44 Binney Street, Smith 353, Boston, MA 02115, USAHarry C. Brastianos, Department of Oncology, Johns Hopkins University, 1550 Orleans Street, Baltimore, MD 21231, USAWesley Hsu, Departme...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5087233</comments>
            <pubDate>Tue, 26 Jul 2011 05:48:23 +0100</pubDate>
            <guid isPermaLink="false">5087233</guid>        </item>
        <item>
            <title>Primary intracranial plasma cell granulomas presenting as malignant neoplasms</title>
            <link>http://www.medworm.com/index.php?rid=5063307&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fg71g3576v7822003%2F</link>
            <description>We report two additional cases of intracranial PCG exclusively involving the brain parenchyma.
 A 47&amp;nbsp;year-old woman, presenting with partial motor seizures and fluent aphasia, underwent complete excision of a well-demarcated,
 enhancing left parietal mass. The second patient was a 56&amp;nbsp;year-old man presenting with headaches and right-sided weakness
 who underwent stereotactic biopsy of an ill-defined, heterogeneously enhancing lesion in the left basal ganglia. Immunohistochemical
 analysis of surgical specimens showed polyclonal plasma cells and mature lymphocytes but no etiological agent. A histopathologic
 diagnosis of intracranial PCG was made in both cases. PCG should be part of the differential diagnosis of enhancing mass lesions
 of the brain. The etiology and natural history...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5063307</comments>
            <pubDate>Sat, 23 Jul 2011 15:49:35 +0100</pubDate>
            <guid isPermaLink="false">5063307</guid>        </item>
        <item>
            <title>Combination of neoadjuvant chemotherapy followed by surgical resection as a new strategy for WHO grade II gliomas: a study of cognitive status and quality of life</title>
            <link>http://www.medworm.com/index.php?rid=5063308&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fb7l0x534638597m6%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Diffuse WHO grade II (GIIG) may be unresectable when involving critical structures. To assess the feasibility and functional
 tolerance (cognition and quality of life) of an original therapeutic strategy combining neoadjuvant chemotherapy followed
 by surgical resection for initially inoperable GIIG. Ten patients underwent Temozolomide for unresectable GIIG, as initial
 treatment or at recurrence after previous partial resection, due to invasion of eloquent areas or bi-hemispheric diffusion
 preventing a total/subtotal removal. Functional outcome after both treatments was assessed, with evaluation of seven cognitive
 domains. Chemotherapy induced tumor shrinkage (median volume decrease 38.9%) in ipsilateral functional areas in six patients
 and in the contralateral hemi...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5063308</comments>
            <pubDate>Fri, 22 Jul 2011 17:04:24 +0100</pubDate>
            <guid isPermaLink="false">5063308</guid>        </item>
        <item>
            <title>Revisiting the role of molecular targeted therapies in patients with brain metastases</title>
            <link>http://www.medworm.com/index.php?rid=5063309&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fjx0vg42128881384%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Brain metastases (BM) are treated with surgical resection when feasible. Unfortunately this occurs only in a small subset
 of patients. The optimal treatment for patients with intracranial metastases non amenable to surgical resection has not been
 identified. Radiotherapy improves symptom control and survival but long-term local control has been poor. Conventional chemotherapies
 have generally produced disappointing results possibly due to their limited ability to penetrate the blood brain barrier.
 Therefore, newer treatments are required for patients with unresectable BM. Targeted therapies such as bevacizumab, erlotinib,
 gefitinib, sunitinib and sorafenib, are all licensed and have demonstrated improved survival in patients with metastatic disease.
 In this review...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5063309</comments>
            <pubDate>Fri, 22 Jul 2011 17:04:22 +0100</pubDate>
            <guid isPermaLink="false">5063309</guid>        </item>
        <item>
            <title>Chronic lymphocytic leukemia with central nervous system involvement: report of two cases with a comprehensive literature review</title>
            <link>http://www.medworm.com/index.php?rid=5063310&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fw751883803865566%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Central nervous system (CNS) involvement is a rare complication of chronic lymphocytic leukemia (CLL) with varied outcomes.
 We contribute two additional cases of CLL with CNS involvement. The clinical course and response to treatment are described.
 All 78 previously reported cases of CLL with CNS involvement are presented in this comprehensive review of the literature.
 CNS involvement of CLL is a rare complication that does not seem to correlate with any evident risk factors. Resolution of
 CNS symptoms can often be accomplished with intrathecal chemotherapy or irradiation. Early detection and treatment may result
 in better outcomes in this rare complication.
 
 
	Content Type Journal ArticlePages 1-16DOI 10.1007/s11060-011-0636-zAuthors
		Alan A. Moazzam, Departmen...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5063310</comments>
            <pubDate>Tue, 19 Jul 2011 06:41:17 +0100</pubDate>
            <guid isPermaLink="false">5063310</guid>        </item>
        <item>
            <title>Modification of loco-regional microenvironment in brain tumors by spinal cord stimulation. Implications for radio-chemotherapy</title>
            <link>http://www.medworm.com/index.php?rid=5030054&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fbu5763712012v303%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The effectiveness of radiotherapy and chemotherapy in high grade gliomas (HGG) depends on tumor micro-environment. We summarize
 our experience of the influence of spinal cord stimulation (SCS) on this micro-environment. Patients with HGG (n&amp;nbsp;=&amp;nbsp;26) were assessed pre- and post-SCS, using: (1) Doppler in middle cerebral arteries (MCA) and (2) in common carotid arteries
 (CCA); (3) tumor blood-flow using single photon emission computed tomography (SPECT); (4) tumor-pO2 (mmHg) using polarographic probes (eight tumor areas from five patients); and (5) tumor glucose metabolism using 18F-fluoro-2-deoxyglucose (18FDG) positron emission tomography (18FDG-PET). Pre-SCS: tumor blood-flow was lower (P&amp;nbsp;&amp;lt;&amp;nbsp;0.001) than peri-tumor areas and healthy contra-lateral a...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5030054</comments>
            <pubDate>Tue, 12 Jul 2011 05:57:03 +0100</pubDate>
            <guid isPermaLink="false">5030054</guid>        </item>
        <item>
            <title>Using different schedules of Temozolomide to treat low grade gliomas: systematic review of their efficacy and toxicity</title>
            <link>http://www.medworm.com/index.php?rid=5030055&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fj493v310n8pg87t5%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Low grade gliomas (LGG) contribute to 50% of all central nervous tumors in children and 15% of all gliomas in adults. Temozolomide
 (TMZ) is an oral alkylating agent with activity in high and LGG. Various regimens of TMZ are currently in use. We attempted
 to assess the impact of different TMZ regimens on the treatment of LGG. A systematic review of the literature identified all
 the studies published in Pubmed, EMBASE and Cochrane databases which met the inclusion criteria. The primary outcome measure
 was the impact of different TMZ regimens on the 12&amp;nbsp;month progression-free survival (PFS) rates of patients diagnosed with
 progressive LGG. Secondary outcome measures looked at the ability of the three regimens to elicit an objective response and
 the associated tox...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5030055</comments>
            <pubDate>Tue, 12 Jul 2011 05:57:01 +0100</pubDate>
            <guid isPermaLink="false">5030055</guid>        </item>
        <item>
            <title>Phase I study of sunitinib and irinotecan for patients with recurrent malignant glioma</title>
            <link>http://www.medworm.com/index.php?rid=5020054&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F912322341476634u%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;We determined the maximum tolerated dose (MTD) and dose-limiting toxicities (DLT) of the oral vascular endothelial growth
 factor receptor (VEGFR) inhibitor, sunitinib, when administered with irinotecan among recurrent malignant glioma (MG) patients.
 For each 42-day cycle, sunitinib was administered once a day for four consecutive weeks followed by a 2 week rest. Irinotecan
 was administered intravenously every other week. Each agent was alternatively escalated among cohorts of 3–6 patients enrolled
 at each dose level. Patients on CYP3A-inducing anti-epileptic drugs were not eligible. Twenty-five patients with recurrent
 MG were enrolled, including 15 (60%) with glioblastoma (GBM) and 10 (40%) with grade 3 MG. Five patients progressed previously
 on bevacizumab and ...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5020054</comments>
            <pubDate>Sat, 09 Jul 2011 06:18:14 +0100</pubDate>
            <guid isPermaLink="false">5020054</guid>        </item>
        <item>
            <title>Gefitinib induces apoptosis in human glioma cells by targeting Bad phosphorylation</title>
            <link>http://www.medworm.com/index.php?rid=5020053&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fh7744u272q5v0208%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Gefitinib, a selective epidermal growth factor receptor tyrosine kinase inhibitor, is under clinical testing and use in cancer
 patients, including glioma. However, the molecular mechanisms involved in gefitinib-mediated anticancer effects against glioma
 remain largely uncharacterized. Gefitinib inhibits cell growth and induces apoptosis in human glioma cells. Gefitinib also
 induces death of H4 cells with characteristics of the intrinsic apoptotic pathway, including Bax mitochondrial translocation,
 mitochondrial outer membrane permeabilization, cytochrome c cytosolic release, and caspase-9/caspase-3 activation. The importance
 of Bax in mediating gefitinib-induced apoptosis was confirmed by the attenuation of apoptosis by Bax siRNA and Bax channel
 blocker. Gefitinib...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5020053</comments>
            <pubDate>Sat, 09 Jul 2011 06:18:14 +0100</pubDate>
            <guid isPermaLink="false">5020053</guid>        </item>
        <item>
            <title>A functional polymorphism in the pre-miR-146a gene is associated with risk and prognosis in adult glioma</title>
            <link>http://www.medworm.com/index.php?rid=5020056&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F066t6j7033104286%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;MicroRNAs (miRNAs) are non-coding RNAs that function as post-transcriptional regulators of tumor suppressors and oncogenes.
 Single nucleotide polymorphisms (SNPs) in miRNAs may contribute to carcinogenesis by altering expression of miRNAs and their
 targets. A G&amp;gt;C polymorphism (rs2910164) in the miR-146a precursor sequence leads to a functional change associated with the risk for numerous malignancies. A role for this SNP in
 glioma pathogenesis has not yet been examined. We investigated whether rs2910164 genotypes influence glioma risk and prognosis
 in a multi-center case–control study comprised of 593 Caucasian glioma cases and 614 community-based controls. Unconditional
 logistic regression was used to estimate odds ratios (OR) and 95% confidence intervals (CI...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5020056</comments>
            <pubDate>Sat, 09 Jul 2011 06:18:13 +0100</pubDate>
            <guid isPermaLink="false">5020056</guid>        </item>
        <item>
            <title>A new tool for grade II glioma studies: plotting cumulative time with quality of life versus time to malignant transformation</title>
            <link>http://www.medworm.com/index.php?rid=5020055&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F073105987n270644%2F</link>
            <description>A new tool for grade II glioma studies: plotting cumulative time with quality of life versus time to malignant transformation
	Content Type Journal ArticlePages 1-3DOI 10.1007/s11060-011-0659-5Authors
		Emmanuel Mandonnet, Department of Neurosurgery, Hôpital Lariboisière, 2 rue Ambroise Paré, 75010 Paris, FranceHugues Duffau, Department of Neurosurgery, Hôpital Gui de Chauliac, Montpellier, FranceLuc Bauchet, Department of Neurosurgery, Hôpital Gui de Chauliac, Montpellier, France
	

	
		Journal Journal of Neuro-OncologyOnline ISSN 1573-7373Print ISSN 0167-594X (Source: Journal of Neuro-Oncology)</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5020055</comments>
            <pubDate>Sat, 09 Jul 2011 06:18:13 +0100</pubDate>
            <guid isPermaLink="false">5020055</guid>        </item>
        <item>
            <title>Prophylactic intrathecal chemotherapy in primary CNS lymphoma</title>
            <link>http://www.medworm.com/index.php?rid=5020057&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ft43p84w01568078h%2F</link>
            <description>We report a retrospective single center study of a cohort of 69 patients with primary central nervous system lymphoma who
 had been treated with a regimen that combined high intravenous doses of Methotrexate, CCNU, procarbazine and methylprednisolone.
 Before 2000, patients systematically received intrathecal prophylaxis including Methotrexate, cytarabine, and hydrocortisone
 delivered either by intraventricular or lumbar injection along with the systemic chemotherapy (group A, n&amp;nbsp;=&amp;nbsp;39). After this date, the procedure was changed and intrathecal chemotherapy was withdrawn from the protocol (group B,
 n&amp;nbsp;=&amp;nbsp;30). The median age and Karnofsky index were comparable in both groups. At the time of analysis, we found no significant
 difference between patients with and without in...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5020057</comments>
            <pubDate>Fri, 08 Jul 2011 06:30:03 +0100</pubDate>
            <guid isPermaLink="false">5020057</guid>        </item>
        <item>
            <title>Cilengitide in patients with recurrent glioblastoma: the results of NABTC 03-02, a phase II trial with measures of treatment delivery</title>
            <link>http://www.medworm.com/index.php?rid=5020058&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F3873l24l703u3541%2F</link>
            <description>This study was designed to evaluate the efficacy
 and tumor delivery of cilengitide in patients with recurrent glioblastoma. Patients with recurrent glioblastoma who require
 a surgical resection for optimal clinical care received 3 intravenous doses of cilengitide at either 500 or 2000&amp;nbsp;mg (day -8,
 -4, -1) prior to undergoing tumor resection with corresponding blood samples for plasma to tumor comparisons. After recovery
 from surgery, patients were treated with cilengitide (2000&amp;nbsp;mg i.v. twice weekly, maximum of 2&amp;nbsp;years of treatment). The study
 accrued 30 patients with recurrent glioblastoma, 26 were evaluable for efficacy. The 6-month progression free survival rate
 was 12%. Cilengitide was detected in all tumor specimens with higher levels in the group receiving 2000&amp;nbs...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5020058</comments>
            <pubDate>Fri, 08 Jul 2011 06:30:02 +0100</pubDate>
            <guid isPermaLink="false">5020058</guid>        </item>
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