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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, 17 Mar 2010 13:52:21 +0100</lastBuildDate>
        <item>
            <title>Erratum to: Glioblastoma cell growth is suppressed by disruption of fibroblast growth factor pathway signaling</title>
            <link>http://www.medworm.com/index.php?rid=3360339&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F248j1021v0072633%2F</link>
            <description>Content Type Journal ArticleCategory ErratumDOI 10.1007/s11060-010-0155-3Authors
		Watcharin Loilome, Johns Hopkins University Department of Neurosurgery, School of Medicine Baltimore MD 21231 USAAvadhut D. Joshi, Johns Hopkins University Department of Neurosurgery, School of Medicine Baltimore MD 21231 USAColette M. J. ap Rhys, Johns Hopkins University Department of Neurosurgery, School of Medicine Baltimore MD 21231 USASara Piccirillo, Università degli Studi Bicocca-Millan Milan 20126 ItalyAngelo L. Vescovi, Università degli Studi Bicocca-Millan Milan 20126 ItalyGary L. Gallia, Johns Hopkins University Department of Neurosurgery, School of Medicine Baltimore MD 21231 USAGregory J. Riggins, Johns Hopkins University Department of Neurosurgery, School of Medicine Baltimore MD 21231 USA
...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3360339</comments>
            <pubDate>Thu, 11 Mar 2010 02:43:21 +0100</pubDate>
            <guid isPermaLink="false">3360339</guid>        </item>
        <item>
            <title>Phase II TPDCV protocol for pediatric low-grade hypothalamic/chiasmatic gliomas: 15-year update</title>
            <link>http://www.medworm.com/index.php?rid=3360340&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fh309u6591128643j%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;To report long-term results for children with low-grade hypothalamic/chiasmatic gliomas treated on a phase II chemotherapy
 protocol. Between 1984 and 1992, 33 children with hypothalamic/chiasmatic LGGs received TPDCV chemotherapy on a phase II prospective
 trial. Median age was 3.0&amp;nbsp;years (range 0.3–16.2). Twelve patients (36%) underwent STRs, 14 (42%) biopsy only, and seven (21%)
 no surgery. Twenty patients (61%) had pathologic JPAs, nine (27%) grade II gliomas, and four (12%) no surgical sampling. Median
 f/u for surviving patients was 15.2&amp;nbsp;years (range 5.3–20.7); 20 of the 23 surviving patients had 14 or more years of follow-up.
 Fifteen-year PFS and OS were 23.4 and 71.2%, respectively. Twenty-five patients progressed, of whom 13 are NED, two are AWD,...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3360340</comments>
            <pubDate>Thu, 11 Mar 2010 02:43:20 +0100</pubDate>
            <guid isPermaLink="false">3360340</guid>        </item>
        <item>
            <title>Neoadjuvant targeting of glioblastoma multiforme with radiolabeled DOTAGA–substance P—results from a phase I study</title>
            <link>http://www.medworm.com/index.php?rid=3355554&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fj71x868380u761h6%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Complete surgical resection beyond tumor margins cannot be achieved in glioblastoma multiforme (GBM) because of infiltrative
 nature. In several cancers, neoadjuvant treatment has been implemented to reduce the risk of tumor cell spreading during resection.
 In GBM, the objective of a neoadjuvant approach is reduction of tumor cells within the main tumor mass and beyond in the infiltration
 zone. Such an approach can only be performed if elevated intracranial pressure can be medically controlled. In a previous
 study with recurrent gliomas, we showed that local intratumoral injection of radiolabeled DOTAGA–substance P substantially
 inhibited further growth and led to radionecrotic transformation of the tumor (CCR 2006). We have now examined this modality
 as neoadjuv...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3355554</comments>
            <pubDate>Wed, 10 Mar 2010 16:00:43 +0100</pubDate>
            <guid isPermaLink="false">3355554</guid>        </item>
        <item>
            <title>CDC25A mRNA levels significantly correlate with Ki-67 expression in human glioma samples</title>
            <link>http://www.medworm.com/index.php?rid=3355555&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F23287nwp11318863%2F</link>
            <description>This study evaluated the role of CDC25 phosphatases in human glioma proliferation. Upregulation of CDC25A
 was observed in human glioma specimens and human glioma cell lines. Comparison of expression levels of CDC25A and CDC25B messenger
 ribonucleic acid (RNA) to Ki-67 labeling index in glioma tissues found that Ki-67 labeling index was significantly correlated
 with the expression of CDC25A, but not with that of CDC25B. Depletion of CDC25A by small interfering RNA and inhibition of
 CDC25 suppressed cell proliferation and induced apoptosis in glioma cell lines, indicating that CDC25A is a potential target
 for the development of new therapy for glioma.
 
 
	Content Type Journal ArticleCategory Laboratory Investigation - Human/Animal TissueDOI 10.1007/s11060-010-0147-3Authors
		Yoji Yamas...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3355555</comments>
            <pubDate>Wed, 10 Mar 2010 16:00:42 +0100</pubDate>
            <guid isPermaLink="false">3355555</guid>        </item>
        <item>
            <title>Decreased pygopus 2 expression suppresses glioblastoma U251 cell growth</title>
            <link>http://www.medworm.com/index.php?rid=3355557&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F9m8138nx2r532626%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Gliomas are common malignant tumors of the human neural system, and Wnt signaling activation is closely related to glioma
 malignancy. Human Pygopus 2 (Pygo2) was recently discovered to be a component of the Wnt signaling pathway, which is required
 for β-catenin/Tcf-dependent transcription. However, the role of Pygo2 in glioblastoma cell growth and survival remains uncertain.
 In the present study, Pygo2 expression was evaluated in 80 glioma tissue samples. Results demonstrated that tumor grade exhibited
 a positive correlation with overexpression of Pygo2. In addition, small hairpin RNA (shRNA) was used to specifically knockdown
 Pygo2 expression in human glioblastoma U251 cell lines. Results showed that inhibition of Pygo2 expression resulted in inhibited
 cell prol...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3355557</comments>
            <pubDate>Wed, 10 Mar 2010 16:00:41 +0100</pubDate>
            <guid isPermaLink="false">3355557</guid>        </item>
        <item>
            <title>Phase 1 clinical trial of bortezomib in adults with recurrent malignant glioma</title>
            <link>http://www.medworm.com/index.php?rid=3355556&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fr70t01m0h34r2477%2F</link>
            <description>This study was conducted to determine
 the side effects and maximum tolerated dose (MTD) of bortezomib in patients with recurrent malignant glioma. Separate dose
 escalations were conducted in patients taking or not taking enzyme-inducing anti-seizure drugs (+/−EIASD). The starting dose
 in both groups was 0.9&amp;nbsp;mg/m2 intravenously twice weekly for the first three of each 4&amp;nbsp;week cycle. Imaging assessment of response was carried out and Plasma
 20S proteasome activity inhibition and imaging was conducted to monitor efficacy. The 66 patients enrolled had a median age
 of 51&amp;nbsp;years, median KPS of 90%, and 77% had glioblastoma multiforme. The MTD in the −EIASD group was 1.70&amp;nbsp;mg/m2 based on grade 3 thrombocytopenia, sensory neuropathy and fatigue. In the +EIASD group escala...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3355556</comments>
            <pubDate>Wed, 10 Mar 2010 16:00:41 +0100</pubDate>
            <guid isPermaLink="false">3355556</guid>        </item>
        <item>
            <title>Late mortality in pediatric patients with craniopharyngioma</title>
            <link>http://www.medworm.com/index.php?rid=3355558&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F1647g2842v70k46q%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Ten year survival rates for patients with craniopharyngioma vary from 24 to 100%. A review of the database of all children
 diagnosed with craniopharyngioma in British Columbia (BC) revealed that several patients died &amp;gt;10&amp;nbsp;years after diagnosis. This
 retrospective study investigates the causes and timing of deaths and reports the overall survival in this population based
 group of patients. A chart review was conducted on all patients aged &amp;lt;17&amp;nbsp;years, diagnosed in BC with craniopharyngioma between
 1967 and 2003. Imaging studies were reviewed by a neuroradiologist. All deaths in the province are reported to a central agency,
 which allowed identification of patients who died after being lost to clinical follow up. Forty-one patients were identified
 with ...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3355558</comments>
            <pubDate>Wed, 10 Mar 2010 16:00:40 +0100</pubDate>
            <guid isPermaLink="false">3355558</guid>        </item>
        <item>
            <title>Factors affecting prognosis of patients with intracranial anaplastic oligodendrogliomas: a single institutional review of 70 patients</title>
            <link>http://www.medworm.com/index.php?rid=3328307&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F0j9771j3x7011540%2F</link>
            <description>In this study, we assessed the
 factors affecting the prognosis of AO patients. Seventy AO patients were recruited from 2001 to 2006 in Shanghai Huashan Hospital
 of Fudan University; all were treated surgically. Kaplan–Meier survival analysis and Cox regression analysis were used to
 analyze the prognostic effects of 14 different factors, which were selected from clinical, radiological, pathological, and
 treatment variables. The results showed that chemotherapy, age, primary or secondary tumors, preoperative Karnofsky Performance
 Scale (KPS) scores, the presence of epilepsy at initial presentation, radiological contrast infusion, and neurological parameters
 all correlated with the prognosis of the patients. Furthermore, Cox multivariate analysis also showed that the age (P&amp;nbsp;&amp;lt;&amp;...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3328307</comments>
            <pubDate>Tue, 02 Mar 2010 10:03:48 +0100</pubDate>
            <guid isPermaLink="false">3328307</guid>        </item>
        <item>
            <title>Coexistence between meningioma and tuberculosis: case report</title>
            <link>http://www.medworm.com/index.php?rid=3323725&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fw8r73537012471h8%2F</link>
            <description>Abstracts&amp;nbsp;&amp;nbsp;Intracranial tuberculoma generally presents as either solitary or multiple lesions in the brain parenchyma. These are characterized
 by a ring-enhancing area on either computerized tomography scans or magnetic resonance images.&amp;nbsp;A 66&amp;nbsp;year-old female with a
 history of breast carcinoma at 41&amp;nbsp;years, treated with radical mastectomy and radio and chemotherapy, and rheumatoid arthritis,
 treated in the last 10&amp;nbsp;years, presented two&amp;nbsp;months ago with occipital headache, nausea, cerebellar syndrome, alterations of
 speech, and memory loss. The TC scan showed occipital enhancement by contrast and surrounded by oedema, suggesting metastasis.
 Histology showed a benign meningioma with many multinuclear giant cells, granulomas, and central caseating necrosis....</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3323725</comments>
            <pubDate>Mon, 01 Mar 2010 18:09:25 +0100</pubDate>
            <guid isPermaLink="false">3323725</guid>        </item>
        <item>
            <title>Podoplanin and LYVE-1 expression in lymphatic vessels of human neuroblastoma</title>
            <link>http://www.medworm.com/index.php?rid=3315450&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fn3813616680540q7%2F</link>
            <description>Content Type Journal ArticleCategory Case ReportDOI 10.1007/s11060-010-0148-2Authors
		Domenico Ribatti, University of Bari Medical School Department of Human Anatomy and Histology Piazza G. Cesare 11, Policlinico 70124 Bari ItalyBeatrice Nico, University of Bari Medical School Department of Human Anatomy and Histology Piazza G. Cesare 11, Policlinico 70124 Bari ItalyAnca Maria Cimpean, “Victor Babes” University of Medicine and Pharmacy Department of Histology and Cytology Pta Eftimie Murgu 2 300041 Timisoara RomaniaMarius Raica, “Victor Babes” University of Medicine and Pharmacy Department of Histology and Cytology Pta Eftimie Murgu 2 300041 Timisoara Romania
	

	
		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=3315450</comments>
            <pubDate>Fri, 26 Feb 2010 09:42:58 +0100</pubDate>
            <guid isPermaLink="false">3315450</guid>        </item>
        <item>
            <title>Huge cranio-cerebral rhabdomyosarcoma in HIV-positive patient</title>
            <link>http://www.medworm.com/index.php?rid=3315451&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F6217503785881475%2F</link>
            <description>Content Type Journal ArticleCategory Case ReportDOI 10.1007/s11060-010-0149-1Authors
		Liverana Lauretti, Catholic University School of Medicine Department of Neurosurgery Largo Agostino Gemelli, 8 00168 Rome ItalyNicola Montano, Catholic University School of Medicine Department of Neurosurgery Largo Agostino Gemelli, 8 00168 Rome ItalyGiovanna Paternoster, Catholic University School of Medicine Department of Neurosurgery Largo Agostino Gemelli, 8 00168 Rome ItalyEduardo Fernandez, Catholic University School of Medicine Department of Neurosurgery Largo Agostino Gemelli, 8 00168 Rome ItalyMariangela Novello, Catholic University School of Medicine Department of Pathology Rome ItalyLibero Lauriola, Catholic University School of Medicine Department of Pathology Rome ItalyRoberto Pallini, Cat...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3315451</comments>
            <pubDate>Fri, 26 Feb 2010 09:42:57 +0100</pubDate>
            <guid isPermaLink="false">3315451</guid>        </item>
        <item>
            <title>Steroid requirements during radiotherapy for malignant gliomas</title>
            <link>http://www.medworm.com/index.php?rid=3315452&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fm306200j87q0217m%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp; Radiotherapy (RT) is the standard treatment for high-grade gliomas. However, toxicity may develop during RT, such as brain
 edema or worsening of neurological symptoms. Surprisingly, no dedicated study had focused on steroid requirements during RT
 in adult patients with malignant gliomas. We evaluated prospectively all patients with malignant gliomas treated by RT in
 a single center from July 2006 to May 2009. Age, sex, initial Karnofsky performance status (KPS), tumor localization and histology,
 type of surgical resection, clinical target volume, total dose and duration of RT, concomitant treatment with temozolomide,
 and steroid dosage during RT and at 1 and 3&amp;nbsp;months after RT were recorded in all patients. Most of the 80 patients (70%) were
 already taking st...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3315452</comments>
            <pubDate>Fri, 26 Feb 2010 06:45:53 +0100</pubDate>
            <guid isPermaLink="false">3315452</guid>        </item>
        <item>
            <title>Treatment induced necrosis versus recurrent/progressing brain tumor: going beyond the boundaries of conventional morphologic imaging</title>
            <link>http://www.medworm.com/index.php?rid=3308097&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fv5w2014028860173%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Brain tumor patients undergo various combinations therapies, leading to very complex and confusing imaging appearances on
 follow up MR imaging and hence, differentiating recurrent or progressing tumors from treatment induced necrosis or effects
 has always been a challenge in neuro-oncologic imaging. This particular topic has become more relevant these days because
 of the advent of newer anti-angiogenic and anti-neoplastic chemotherapeutic agents as well as use of salvage radiation therapy.
 Various clinically available functional imaging modalities can provide additional physiologic and metabolic information about
 the tumors which could be useful in identifying viable tumor from treatment induced necrosis and hence, can guide treatment
 planning. In this review we w...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3308097</comments>
            <pubDate>Wed, 24 Feb 2010 06:50:31 +0100</pubDate>
            <guid isPermaLink="false">3308097</guid>        </item>
        <item>
            <title>Overexpression and activation of epidermal growth factor receptor in hemangioblastomas</title>
            <link>http://www.medworm.com/index.php?rid=3295540&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fw3r725263438vj87%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Hemangioblastomas frequently develop in patients with von Hippel-Lindau (VHL) disease, an autosomal dominant genetic disorder.
 The tumors are characterized by a dense network of blood capillaries, often in association with cysts. Although activation
 of receptor tyrosine kinase (RTK) signaling, including epidermal growth factor receptor (EGFR) has been implicated in the
 development of malignant brain tumors such as high-grade gliomas, little is known about the role of RTK signaling in hemangioblastomas.
 To address this issue, we examined hemangioblastoma tumor specimens using receptor tyrosine kinase (RTK) activation profiling
 and immunohistochemistry. Six human hemangioblastomas were analyzed with a phospho-RTK antibody array, revealing EGFR phosphorylation
 in all...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3295540</comments>
            <pubDate>Sun, 21 Feb 2010 06:55:37 +0100</pubDate>
            <guid isPermaLink="false">3295540</guid>        </item>
        <item>
            <title>Prognostic significance of histological grading, p53 status, YKL-40 expression, and IDH1 mutations in pediatric high-grade gliomas</title>
            <link>http://www.medworm.com/index.php?rid=3295541&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fr338116449867478%2F</link>
            <description>The objective of this study was to evaluate, in a series of 43 pediatric high-grade gliomas (21 anaplastic astrocytoma WHO
 grade III and 22 glioblastoma WHO grade IV), the prognostic value of histological grading and expression of p53 and YKL-40.
 Moreover, mutational screening for TP53 and IDH1 was performed in 27 of 43 cases. The prognostic stratification for histological grading showed no difference in overall (OS)
 and progression-free survival (PFS) between glioblastomas and anaplastic astrocytomas. Overexpression of YKL40 was detected
 in 25 of 43 (58%) cases, but YKL-40 expression was not prognostic in terms of OS and PFS. p53 protein expression was observed
 in 13 of 43 (31%) cases but was not prognostic. TP53 mutations were detected in five of 27 (18%) cases (four glioblastomas a...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3295541</comments>
            <pubDate>Sat, 20 Feb 2010 06:52:48 +0100</pubDate>
            <guid isPermaLink="false">3295541</guid>        </item>
        <item>
            <title>HGF upregulates CXCR4 expression in gliomas via NF-κB: implications for glioma cell migration</title>
            <link>http://www.medworm.com/index.php?rid=3280944&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F91703975662850w0%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Invasion is a hallmark of malignant gliomas and is the main reason for therapeutic failure and recurrence of the tumor. CXCR4
 is a key chemokine receptor implicated in glioma cell migration whose expression is regulated by hypoxia. Here, we report
 that hepatocyte growth factor (HGF) upregulated CXCR4 protein expression in glioma cells. HGF pre-treatment increased migration
 of U87MG and LN229 glioma cells towards the CXCR4 ligand, stromal cell-derived factor-1α (SDF-1α). AMD3100, a CXCR4 inhibitor,
 inhibited the increased migration of HGF pre-treated LN229 glioma cells towards SDF-1α. Following exposure to HGF and hypoxia,
 both cell lines showed nuclear translocation of NF-κB (p65). The HGF- and hypoxia-induced nuclear translocation of NF-κB (p65)
 involved pho...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3280944</comments>
            <pubDate>Tue, 16 Feb 2010 06:41:53 +0100</pubDate>
            <guid isPermaLink="false">3280944</guid>        </item>
        <item>
            <title>Rebound tumour progression after the cessation of bevacizumab therapy in patients with recurrent high-grade glioma</title>
            <link>http://www.medworm.com/index.php?rid=3270394&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F4j4h71v1237202p0%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;After withdrawal of bevacizumab in patients with recurrent high-grade glioma, we have observed a rapid tumour re-growth or
 “rebound” radiographic phenomenon with accelerated clinical decline. We retrospectively reviewed 11 patients treated at the
 Henry Ford Hermelin Brain Tumor Center with recurrent high-grade glioma who demonstrated a rebound progression pattern after
 the discontinuation of bevacizumab. The original tumour area-of-enhancement increased by a mean of 158%, when compared to
 the rebound magnetic resonance imaging. After rebound, no patients (0/8) showed a response to next-line treatments that did
 not include bevacizumab. The median survival of those re-treated with bevacizumab was 149 and 32&amp;nbsp;days for those who received
 other regimens. Abrupt...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3270394</comments>
            <pubDate>Fri, 12 Feb 2010 07:09:58 +0100</pubDate>
            <guid isPermaLink="false">3270394</guid>        </item>
        <item>
            <title>A lower-dose, lower-toxicity cisplatin–etoposide regimen for childhood progressive low-grade glioma</title>
            <link>http://www.medworm.com/index.php?rid=3270393&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fc34647v88t66m727%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;After successfully using cisplatin (30&amp;nbsp;mg/m2/day) and etoposide (150&amp;nbsp;mg/m2/day) in ten three-day courses for progressive low-grade gliomas, a subsequent protocol reduced the daily doses of cisplatin
 (to 25&amp;nbsp;mg) and etoposide (to 100&amp;nbsp;mg), with the objective of achieving the same response and three-year PFS rates with lower
 neurotoxicity and myelotoxicity. We treated 37 patients (median age 6 years); 23 had optochiasmatic tumours and nine were
 metastatic cases. Diagnoses were clinical in 13 cases and histological in 24, and comprised: pilocytic astrocytoma (17), ganglioglioma
 (3), pilomyxoid astrocytoma (2), and fibrillary astrocytoma (2). Treatment was prompted by radiological evidence of progression
 and/or clinical deterioration a median 18&amp;nbsp;...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3270393</comments>
            <pubDate>Fri, 12 Feb 2010 07:09:58 +0100</pubDate>
            <guid isPermaLink="false">3270393</guid>        </item>
        <item>
            <title>Early CNS relapse in a good-risk primary mediastinal large B-cell lymphoma after combined chemo- and radio-therapy</title>
            <link>http://www.medworm.com/index.php?rid=3270395&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fb611j28201526466%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorDOI 10.1007/s11060-010-0132-xAuthors
		Makoto Sasaki, Juntendo University School of Medicine Division of Hematology, Department of Internal Medicine 2-1-1 Hongo, Bunkyo-ku Tokyo 113-8421 JapanKoichi Sugimoto, Juntendo University School of Medicine Division of Hematology, Department of Internal Medicine 2-1-1 Hongo, Bunkyo-ku Tokyo 113-8421 JapanAzuchi Masuda, Juntendo University School of Medicine Division of Hematology, Department of Internal Medicine 2-1-1 Hongo, Bunkyo-ku Tokyo 113-8421 JapanYutaka Tsukune, Juntendo University School of Medicine Division of Hematology, Department of Internal Medicine 2-1-1 Hongo, Bunkyo-ku Tokyo 113-8421 JapanYuriko Yahata, Juntendo University School of Medicine Division of Hematology, Departmen...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3270395</comments>
            <pubDate>Fri, 12 Feb 2010 07:09:57 +0100</pubDate>
            <guid isPermaLink="false">3270395</guid>        </item>
        <item>
            <title>Descriptive epidemiology of selected olfactory tumors</title>
            <link>http://www.medworm.com/index.php?rid=3270396&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F3167132215714400%2F</link>
            <description>The objective of this study was to more fully describe
 selected olfactory tumors using a large population-based cancer incidence database. The Surveillance, Epidemiology and End
 Results (SEER) 9 registries limited-use data were reviewed from 1973 to 2006 for selected nasal cavity (C30.0) and accessory
 sinus (C31.0–31.9) tumors. Frequencies, incidence rates, and relative survival rates were estimated using SEER*Stat, v6.5.2.
 The majority of cases were squamous cell carcinoma (SCC), while the incidence of ON was greater than CND. For ON, the incidence
 was highest in the 60–79&amp;nbsp;year age group, while for SCC, the incidence was highest in the 80+&amp;nbsp;year age group. For CND, the
 incidence leveled off in the oldest age groups. Survival rates were highest for ON (&amp;gt;70% alive at 5...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3270396</comments>
            <pubDate>Fri, 12 Feb 2010 07:09:56 +0100</pubDate>
            <guid isPermaLink="false">3270396</guid>        </item>
        <item>
            <title>Fatal herpetic encephalitis during brain radiotherapy in a cerebral metastasized breast cancer patient</title>
            <link>http://www.medworm.com/index.php?rid=3270397&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ff8r250515713854m%2F</link>
            <description>We present the case of a 55-year-old female who developed HSE type
 1 during brain irradiation and antioedematous dexamethasone treatment for leptomeningeal metastasized breast tumor with epileptic
 seizures. During the radiotherapy (RT), after a total of 32 Gray administrated in 16 fractions, our patient developed cognitive
 impairment and partial epileptic status without fever. Two days later the patient’s clinical conditions had deteriorated and
 high fever manifested. A diagnosis of HSE type 1 was made by a positive cerebrospinal fluid polymerase chain reaction. Antiviral
 therapy with high doses of acyclovir was practiced for four&amp;nbsp;weeks but the comatose state persisted. The patient died 59&amp;nbsp;days
 after the last RT fraction. The temporal relationship of RT to the occurrence ...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3270397</comments>
            <pubDate>Thu, 11 Feb 2010 11:49:30 +0100</pubDate>
            <guid isPermaLink="false">3270397</guid>        </item>
        <item>
            <title>Primary central nervous system Burkitt lymphoma as concomitant lesions in the third and the left ventricles: a case study and literature review</title>
            <link>http://www.medworm.com/index.php?rid=3263842&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fc076hg052u702210%2F</link>
            <description>This study reports the case of a 75-year-old woman with intermittent speech disturbance, headache, and general malaise. Brain
 magnetic resonance imaging showed a double lesion located in the third ventricle and temporal horn of the lateral ventricle.
 We completely removed the lesion in the third ventricle, adhering to the septum pellucidum. The histopathological diagnosis
 was Burkitt lymphoma, which was confirmed to be primary in postoperative investigation. To our knowledge, this is the first
 case of primary Burkitt lymphoma involving cerebral ventricles. Finally, we reviewed the characteristics of primary central
 nervous system Burkitt lymphoma.
 
	Content Type Journal ArticleCategory Case ReportDOI 10.1007/s11060-010-0122-zAuthors
		Ye Gu, Zhongshan Hospital, Fudan University Depar...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3263842</comments>
            <pubDate>Tue, 09 Feb 2010 17:45:31 +0100</pubDate>
            <guid isPermaLink="false">3263842</guid>        </item>
        <item>
            <title>Cranial vault lymphoma: a systematic review of five patients</title>
            <link>http://www.medworm.com/index.php?rid=3263841&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fl6600118227kj564%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Bone involvement is a common finding in many types of lymphoma (Clin Oncol 9(3): 195–196, 1997). However, cranial vault affliction has been regarded as an exceedingly rare presentation, particularly in the case of primary
 lymphoma (J Neurosurg 108(5): 1018–1020, 2008). Our objective is to describe a series of five immunocompetent patients with histologically confirmed cranial vault lymphoma
 (CVL), and to conduct a systematic review of the current literature. Our review points out identical imaging patterns in most
 of the lesions for all reported CVL cases, despite their different histological subtypes. This typical pattern can be seen
 on computed tomography (CT) scans and magnetic resonance imaging (MRI) as an expansive tumor that affects all three compartments
...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3263841</comments>
            <pubDate>Tue, 09 Feb 2010 17:45:31 +0100</pubDate>
            <guid isPermaLink="false">3263841</guid>        </item>
        <item>
            <title>Multiple paraneoplastic diseases occurring in the same patient after thymomectomy</title>
            <link>http://www.medworm.com/index.php?rid=3263840&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fv266504k82151139%2F</link>
            <description>We report on a patient who developed MG after thymomectomy for a malignant thymoma. After MG remission, NMT and Morvan’s syndrome
 occurred, which heralded a mediastinic recurrence, as demonstrated only by autopsy findings.
 
	Content Type Journal ArticleCategory Case ReportDOI 10.1007/s11060-010-0130-zAuthors
		C. Briani, University of Padova Departments of Neurosciences Via Giustiniani, 5 35128 Padova ItalyA. Cagnin, University of Padova Departments of Neurosciences Via Giustiniani, 5 35128 Padova ItalyS. Blandamura, University of Padua Medical Diagnostic Sciences and Special Therapies Padova ItalyG. Altavilla, University of Padua Medical Diagnostic Sciences and Special Therapies Padova Italy
	

	
		Journal Journal of Neuro-OncologyOnline ISSN 1573-7373Print ISSN 0167-594X (Source: Jou...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3263840</comments>
            <pubDate>Tue, 09 Feb 2010 17:45:31 +0100</pubDate>
            <guid isPermaLink="false">3263840</guid>        </item>
        <item>
            <title>Integration of autologous dendritic cell-based immunotherapy in the primary treatment for patients with newly diagnosed glioblastoma multiforme: a pilot study</title>
            <link>http://www.medworm.com/index.php?rid=3263844&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fbup3772252413r07%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Despite resection, radiochemotherapy, and maintenance temozolomide chemotherapy (TMZm), the prognosis of patients with glioblastoma
 multiforme (GBM) remains poor. We integrated immunotherapy in the primary standard treatment for eight pilot adult patients
 (median age 50&amp;nbsp;years) with GBM, to assess clinical and immunological feasibility and toxicity in preparation of a phase I/II
 protocol HGG-2006. After maximum, safe resection, leukapheresis was performed before radiochemotherapy, and four weekly vaccinations
 with autologous GBM lysate-loaded monocyte-derived dendritic cells were given after radiochemotherapy. Boost vaccines with
 lysates were given during TMZm. During the course of vaccination, immunophenotyping showed a relative increase in CD8+CD25+
 cells in...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3263844</comments>
            <pubDate>Tue, 09 Feb 2010 17:45:30 +0100</pubDate>
            <guid isPermaLink="false">3263844</guid>        </item>
        <item>
            <title>A prospective evaluation and literature review of levetiracetam use in patients with brain tumors and seizures</title>
            <link>http://www.medworm.com/index.php?rid=3263843&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fu4327v3444602671%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;To determine the safety and tolerability of IV and oral levetiracetam monotherapy for seizures in brain tumor patients following
 resection. Brain tumor patients undergoing neurosurgery with ≥1 seizure within the preceding month prior to surgery were enrolled
 to receive intravenous levetiracetam for a minimum of 48&amp;nbsp;h, transitioned to oral levetiracetam at the same dose, and followed
 for 1-month after discharge. Patients were assessed daily in the hospital, provided with a seizure diary, and supplied with
 30&amp;nbsp;days of levetiracetam upon discharge. Study patients were telephoned weekly to assess their cognitive status and seizure
 frequency. Of the 17 patients enrolled, the baseline seizure types were tonic clonic, partial, and complex partial with secondary
...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3263843</comments>
            <pubDate>Tue, 09 Feb 2010 17:45:30 +0100</pubDate>
            <guid isPermaLink="false">3263843</guid>        </item>
        <item>
            <title>Leptomeningeal gliomatosis as the initial presentation of gliomatosis cerebri</title>
            <link>http://www.medworm.com/index.php?rid=3263845&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F35263p017146xn05%2F</link>
            <description>We describe the case of a patient who presented with symptoms
 of increased intracranial pressure and diffuse leptomeningeal enhancement in the brain and spinal cord on MRI. After a period
 of surveillance, intraparenchymal lesions developed in association with widespread diffuse infiltration. The diagnosis of
 gliomatosis cerebri with diffuse leptomeningeal gliomatosis was established in hindsight. Initial treatment consisted of six
 cycles of temozolomide chemotherapy. Following radiological progression, the patient received craniospinal radiotherapy. Four
 months later the patient’s symptoms had resolved and MRI demonstrated near complete response of leptomeningeal enhancement
 and intraparenchymal lesions. Six months after radiotherapy, the patient remains clinically well without rad...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3263845</comments>
            <pubDate>Tue, 09 Feb 2010 17:45:29 +0100</pubDate>
            <guid isPermaLink="false">3263845</guid>        </item>
        <item>
            <title>High dose weekly erlotinib achieves therapeutic concentrations in CSF and is effective in leptomeningeal metastases from epidermal growth factor receptor mutant lung cancer</title>
            <link>http://www.medworm.com/index.php?rid=3263847&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F26kq3282500846w0%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Leptomeningeal metastases (LM) occur in 5–10% of patients with solid tumors and are associated with a dismal prognosis. We
 describe LM from lung adenocarcinoma harboring a mutation in the epidermal growth factor receptor (EGFR) gene that confers
 sensitivity to the EGFR tyrosine kinase inhibitors (EGFR-TKIs) erlotinib and gefitinib. The CSF concentration of EGFR-TKIs
 achieved by standard daily dosing may be insufficient for therapeutic effect. However, intermittent (pulsatile) high dose
 administration (1000–1500&amp;nbsp;mg/week) achieves a higher CSF concentration than standard dosing, and successfully controlled LM
 in this patient.
 
	Content Type Journal ArticleCategory Case ReportDOI 10.1007/s11060-010-0128-6Authors
		Jennifer L. Clarke, Memorial Sloan-Kettering...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3263847</comments>
            <pubDate>Tue, 09 Feb 2010 17:45:27 +0100</pubDate>
            <guid isPermaLink="false">3263847</guid>        </item>
        <item>
            <title>Bradykinin increases the permeability of the blood-tumor barrier by the caveolae-mediated transcellular pathway</title>
            <link>http://www.medworm.com/index.php?rid=3263846&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fj531347777568102%2F</link>
            <description>This study thus contributes further to elucidating the molecular mechanism of opening of the
 BTB by BK and provides a theoretical basis for clinical application of BK.
 
	Content Type Journal ArticleCategory Laboratory Investigation - Human/Animal TissueDOI 10.1007/s11060-010-0124-xAuthors
		Li-bo Liu, China Medical University Department of Neurobiology, College of Basic Medicine 110001 Shenyang Liaoning Province People’s Republic of ChinaYi-xue Xue, China Medical University Department of Neurobiology, College of Basic Medicine 110001 Shenyang Liaoning Province People’s Republic of ChinaYun-hui Liu, China Medical University Department of Neurosurgery, Shengjing Hospital 110004 Shenyang People’s Republic of China
	

	
		Journal Journal of Neuro-OncologyOnline ISSN 1573-7373Print ISSN...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3263846</comments>
            <pubDate>Tue, 09 Feb 2010 17:45:27 +0100</pubDate>
            <guid isPermaLink="false">3263846</guid>        </item>
        <item>
            <title>Biphasic paraneoplastic brainstem encephalitis associated with anti-Ri antibody</title>
            <link>http://www.medworm.com/index.php?rid=3255806&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F676w1p7x1243677x%2F</link>
            <description>We describe a patient with brainstem encephalitis who had elevated
 anti-Ri antibody levels and double-step neurological deterioration associated with different abnormal lesions on MRI. Immunosuppression
 with steroids and intravenous immune globulin combined with aggressive treatment of the tumor successfully led to the resolution
 of brainstem symptoms and MRI lesions. In patients with unusual signs and symptoms of paraneoplastic encephalitis mimicking
 multiple sclerosis, onconeural antibody studies are recommended.
 
	Content Type Journal ArticleCategory Case ReportDOI 10.1007/s11060-010-0135-7Authors
		Kin Tesseki, Nara Medical University Department of Neurology 840 Shijo-cho, Kashihara Nara 634-8522 JapanHiroshi Kataoka, Nara Medical University Department of Neurology 840 Shijo-cho, ...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3255806</comments>
            <pubDate>Mon, 08 Feb 2010 17:31:23 +0100</pubDate>
            <guid isPermaLink="false">3255806</guid>        </item>
        <item>
            <title>Patterns of enrollment of infants with central nervous system tumours on cooperative group studies: a report from the canadian pediatric brain tumour consortium</title>
            <link>http://www.medworm.com/index.php?rid=3247892&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F911110r024408170%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;In children under the age of 3, the most common solid tumours are brain tumors. Treatment for many of these patients includes
 surgery, chemotherapy and rarely radiation therapy. Many clinical trials have been performed in an attempt to establish the
 best treatment for these patients. Patients enrolled on clinical trials contribute to the establishment of the best therapy.
 We performed a national survey of all children less than the age of three with brain tumours and examined the contribution
 these patients made to clinical trials. A data bank was established using data collected from Canadian pediatric oncology
 centers on children less than age 3 diagnosed with brain tumours between 1990 and 2005. Data were collected on the use of
 adjunctive treatment after surge...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3247892</comments>
            <pubDate>Fri, 05 Feb 2010 06:59:54 +0100</pubDate>
            <guid isPermaLink="false">3247892</guid>        </item>
        <item>
            <title>Vorinostat enhances the cytotoxic effects of the topoisomerase I inhibitor SN38 in glioblastoma cell lines</title>
            <link>http://www.medworm.com/index.php?rid=3247893&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F1517316356qt473r%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Histone deacetylase (HDAC) inhibitors represent a promising class of anti-cancer agents that are actively being evaluated
 in the context of clinical trials in solid tumors, including glioblastoma. What makes these agents particularly attractive
 is their capacity to enhance the activity of commonly used cytotoxics in cancer therapy, including both chemotherapy and ionizing
 radiation. As recent investigations suggest HDAC inhibitors may potentiate the cytotoxicity of topoisomerase inhibitors, which
 continue to be a commonly used class of agents in the treatment of glioblastoma, we performed preclinical studies to determine
 if this combination may be a promising strategy in glioblastoma. The effects of the HDAC inhibitor vorinostat and SN38, which
 is the active metab...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3247893</comments>
            <pubDate>Fri, 05 Feb 2010 06:59:53 +0100</pubDate>
            <guid isPermaLink="false">3247893</guid>        </item>
        <item>
            <title>Erratum to: Hepatocyte growth factor production is stimulated by gangliosides and TGF-β isoforms in human glioma cells</title>
            <link>http://www.medworm.com/index.php?rid=3228477&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fjr178842998668p3%2F</link>
            <description>Content Type Journal ArticleCategory Retraction NoteDOI 10.1007/s11060-010-0120-1Authors
		Sheng-hua Chu, NO. 3 People’s Hospital Affiliated to Shanghai Jiao Tong University School of Medicine Department of Neurosurgery Shanghai 201900 ChinaYan-bin Ma, NO. 3 People’s Hospital Affiliated to Shanghai Jiao Tong University School of Medicine Department of Neurosurgery Shanghai 201900 ChinaHong Zhang, NO. 3 People’s Hospital Affiliated to Shanghai Jiao Tong University School of Medicine Department of Neurosurgery Shanghai 201900 ChinaDong-fu Feng, NO. 3 People’s Hospital Affiliated to Shanghai Jiao Tong University School of Medicine Department of Neurosurgery Shanghai 201900 ChinaZhi-an Zhu, NO. 3 People’s Hospital Affiliated to Shanghai Jiao Tong University School of Medicine Depar...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3228477</comments>
            <pubDate>Fri, 29 Jan 2010 17:59:13 +0100</pubDate>
            <guid isPermaLink="false">3228477</guid>        </item>
        <item>
            <title>Chordoid meningioma: a report of ten cases</title>
            <link>http://www.medworm.com/index.php?rid=3205687&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F170j23w64321181u%2F</link>
            <description>This study was done to document the clinical and pathological
 features of ten patients with chordoid meningioma who submitted to surgery at the National Institute of Neurology and Neurosurgery
 in Mexico City. Clinical, histological and immunohistochemical features were examined. The age range was from 30 to 67&amp;nbsp;years
 old (mean, 34.2&amp;nbsp;years). Seven patients were female and three male. The duration of symptoms varied from 3.5&amp;nbsp;months to 5&amp;nbsp;years
 (mean, 14.1&amp;nbsp;months). No systemic symptoms were noted. The tumor was localized in eight cases in the supratentorial compartments.
 Histologically, the tumors were characterized by strands and cords of meningothelial cells arranged in a mucinous stroma.
 Two of the ten tumors showed metaplasic changes, and seven showed brain in...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3205687</comments>
            <pubDate>Fri, 22 Jan 2010 10:10:42 +0100</pubDate>
            <guid isPermaLink="false">3205687</guid>        </item>
        <item>
            <title>Correlation of l-methyl-11C-methionine (MET) uptake with l-type amino acid transporter 1 in human gliomas</title>
            <link>http://www.medworm.com/index.php?rid=3205688&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fh874t1837l56m674%2F</link>
            <description>In conclusion,
 MET SUVmax correlates with LAT1 expression in the tumor in newly diagnosed gliomas. MET transport may be increased by an increased
 number of microvessels combined with a higher density or activity of LAT1 in the tumor endothelial cells in high-grade gliomas.
 Use of MET-PET as a molecular target combined with anti-angiogenesis in glioma therapy should be addressed in future studies.
 
	Content Type Journal ArticleCategory Clinical Study - Patient StudyDOI 10.1007/s11060-010-0117-9Authors
		Shuichi Okubo, Kagawa University Department of Neurological Surgery, Faculty of Medicine 1750-1 Miki-cho, Kita-gun Kagawa 761-0793 JapanHai-Ning Zhen, Kagawa University Department of Neurological Surgery, Faculty of Medicine 1750-1 Miki-cho, Kita-gun Kagawa 761-0793 JapanNobuyuki Kawai, ...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3205688</comments>
            <pubDate>Thu, 21 Jan 2010 10:43:28 +0100</pubDate>
            <guid isPermaLink="false">3205688</guid>        </item>
        <item>
            <title>Germinomas in the basal ganglia: magnetic resonance imaging classification and the prognosis</title>
            <link>http://www.medworm.com/index.php?rid=3194911&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fl275h19121266395%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Germinoma in the basal ganglia (BG) is notorious for its diagnostic difficulty. Clinical and radiological features of this
 disease are quite diverse, but have not been well characterized with respect to prognosis. We retrospectively reviewed the
 clinical course and treatment outcomes of 17 patients with a BG germinoma. The initial magnetic resonance imaging (MRI) features
 were classified. Clinical features and treatment outcomes were then analyzed with this classification scheme. A Type 1 lesion
 was defined as a subtle lesion with faint or no contrast enhancement (six patients). Type 2, 3, and 4 lesions were defined
 as contrast-enhancing lesions and were differentiated by the lesion size and the presence of subependymal seeding (11 patients).
 Type 1 lesions were d...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3194911</comments>
            <pubDate>Wed, 20 Jan 2010 06:45:04 +0100</pubDate>
            <guid isPermaLink="false">3194911</guid>        </item>
        <item>
            <title>Gamma Knife stereotactic radiosurgery for intracranial hemangiopericytomas</title>
            <link>http://www.medworm.com/index.php?rid=3194912&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fj453006u132h4853%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The purpose of this study is to determine the efficacy of Gamma Knife stereotactic radiosurgery (GK SRS) for intracranial
 hemangiopericytomas, and to investigate the optimal dose for successful tumor control without adverse effects. We evaluated
 17 hemangiopericytomas of nine patients treated with GK SRS between 1999 and 2008. The mean tumor volume was 2.2&amp;nbsp;cm3 (range 0.2–9.9&amp;nbsp;cm3), and the mean and median marginal doses were 18.1 and 20&amp;nbsp;Gy (range 11–22&amp;nbsp;Gy), respectively, at the 50% isodose line. Mean
 clinical and radiological follow-up periods were 49 and 34&amp;nbsp;months, respectively. Successful tumor control was achieved in
 14 of 17 lesions (82.4%) at time of last follow-up after GK SRS. Actuarial local tumor control rates at 1, 2, and 5&amp;nbsp...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3194912</comments>
            <pubDate>Tue, 19 Jan 2010 06:45:23 +0100</pubDate>
            <guid isPermaLink="false">3194912</guid>        </item>
        <item>
            <title>Clinicopathologic and immunohistochemical study of choroid plexus tumors: single-institution experience in Mexican population</title>
            <link>http://www.medworm.com/index.php?rid=3190397&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fwq32j5h52h74x341%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;In recent years, few studies have specifically focused on only histological features in choroid plexus tumors. We retrospectively
 reviewed the clinicopathologic and histological features in 37 patients with choroid plexus tumors and correlated these with
 glial fibrillary acidic protein (GFAP) expression and proliferation cell nuclear antigen (PCNA), p53, p21, and Rb labeling
 indexes, with special attention to tumor recurrence/regrowth. The study included 24 choroid plexus papillomas (CPPs), 4 atypical
 choroid plexus papillomas (ACPPs), and 9 choroid plexus carcinomas (CPCs). Patient age ranged from 15 to 70&amp;nbsp;years (mean 44&amp;nbsp;years).
 Most of the choroid plexus tumors were located in the IV ventricle. Recurrence was observed in 21 (52%) cases, 14 of which
 wer...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3190397</comments>
            <pubDate>Fri, 15 Jan 2010 18:00:58 +0100</pubDate>
            <guid isPermaLink="false">3190397</guid>        </item>
        <item>
            <title>A novel pre-clinical in vivo mouse model for malignant brain tumor growth and invasion</title>
            <link>http://www.medworm.com/index.php?rid=3177037&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fr1372618w1802573%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Glioblastoma multiforme (GBM) is a rapidly progressive disease of morbidity and mortality and is the most common form of primary
 brain cancer in adults. Lack of appropriate in vivo models has been a major roadblock to developing effective therapies for
 GBM. A new highly invasive in vivo GBM model is described that was derived from a spontaneous brain tumor (VM-M3) in the VM
 mouse strain. Highly invasive tumor cells could be identified histologically on the hemisphere contralateral to the hemisphere
 implanted with tumor cells or tissue. Tumor cells were highly expressive for the chemokine receptor CXCR4 and the proliferation
 marker Ki-67 and could be identified invading through the pia mater, the vascular system, the ventricular system, around neurons,
 and over whi...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3177037</comments>
            <pubDate>Wed, 13 Jan 2010 06:43:57 +0100</pubDate>
            <guid isPermaLink="false">3177037</guid>        </item>
        <item>
            <title>Malignant sweat gland tumor presenting as an unusual dural-based lesion: case report</title>
            <link>http://www.medworm.com/index.php?rid=3168477&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fq327m77372835270%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Malignant sweat gland tumors are rare neoplasms with high recurrence and metastasis rates of over 50%. Clinically, they are
 often either not diagnosed or diagnosed improperly and are encountered as a histological surprise. Herein, we report a 50-year-old
 woman who suffered from chronic headaches and a left-side limping gait. Magnetic resonance imaging revealed a T1 and T2 heterogeneous
 intense dural-based lesion at right-frontal convexity. The pathological diagnosis of papillary meningioma was rendered at
 the time. Because there was no evidence of residual tumor, tumor recurrence, or distant metastases during the three-year follow-up,
 the clinician believed questioning the initial diagnosis was warranted. After pathological review, the final diagnosis was
 low-grad...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3168477</comments>
            <pubDate>Tue, 12 Jan 2010 18:19:32 +0100</pubDate>
            <guid isPermaLink="false">3168477</guid>        </item>
        <item>
            <title>Immunohistological profiling by B-cell differentiation status of primary central nervous system lymphoma treated by high-dose methotrexate chemotherapy</title>
            <link>http://www.medworm.com/index.php?rid=3168478&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F855p628345r0pw10%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Primary central nervous system lymphoma (PCNSL) remains a devastating disease with poor prognosis, despite the improvement
 offered by methotrexate (MTX)-based chemotherapy. Several studies have attempted to identify biomarkers predictive of prognosis,
 which are expected to be both clinically useful and biologically important for understanding PCNSL. The present study attempts
 to classify human immunodeficiency virus (HIV)-unrelated PCNSL patients treated with radiation combined with rapid high-dose
 MTX chemotherapy according to B-cell differentiation status, and retrospectively examines the prognostic impact. Initial response
 to MTX was a strong predictor of favorable prognosis in terms of both progression-free survival (PFS) and overall survival
 (OS). Thirteen ou...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3168478</comments>
            <pubDate>Tue, 12 Jan 2010 18:19:31 +0100</pubDate>
            <guid isPermaLink="false">3168478</guid>        </item>
        <item>
            <title>A complex karyotype including a t(2;11) in a paediatric ependymoma: case report and review of the literature</title>
            <link>http://www.medworm.com/index.php?rid=3168479&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fy352252m28188244%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Ependymomas are glial tumours representing approximately 5–10% of all intracranial tumours and are the third most common primary
 brain tumour in childhood. Only a few karyotypic studies on paediatric ependymomas have been published and no specific chromosomal
 aberration has been specifically related to this type of cancer. We performed cytogenetic analysis of an ependymoma in an
 11-year-old boy. Our patient showed a complex karyotype, characterized by a near-tetraploidy and a sole structural unbalanced
 aberration: der(2)t(2;11)(q11.2;q13.1), which has not been described before. We here discuss such cytogenetic findings, comparing
 our data with those reported in the literature.
 
	Content Type Journal ArticleCategory Case ReportDOI 10.1007/s11060-009-0108-xAuthors...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3168479</comments>
            <pubDate>Tue, 12 Jan 2010 06:45:10 +0100</pubDate>
            <guid isPermaLink="false">3168479</guid>        </item>
        <item>
            <title>Metronomic treatment of malignant glioma xenografts with irinotecan (CPT-11) inhibits angiogenesis and tumor growth</title>
            <link>http://www.medworm.com/index.php?rid=3168480&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F75766r4105274628%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Irinotecan (CPT-11) has shown emerging promise in the treatment of malignant gliomas. It is believed the mechanism of action
 of irinotecan is to sensitize glioma cells to the cytotoxic action of radiation therapy and alkylating agents. However, clinical
 trials using weekly or three-weekly doses of CPT-11 have demonstrated imaging responses in only 10–15% of patients. In this
 study, we evaluated another mechanism of action, angiosuppression by CPT-11 of ACNU-resistant gliomas, using a metronomic
 administration schedule. Two different types of treatment, (1) conventional and (2) metronomic, were applied to the subcutaneous
 U87 model. We found that metronomic administration of CPT-11 significantly inhibited malignant glioma growth by inhibiting
 angiogenesis; this t...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3168480</comments>
            <pubDate>Tue, 12 Jan 2010 06:45:09 +0100</pubDate>
            <guid isPermaLink="false">3168480</guid>        </item>
        <item>
            <title>Glioblastoma simultaneously present with adjacent meningioma: case report and review of the literature</title>
            <link>http://www.medworm.com/index.php?rid=3168481&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fl36w611433084881%2F</link>
            <description>We present a case of two primary intracranial tumors occurring
 simultaneously at adjacent sites. Preoperative gadolinium-enhanced magnetic resonance imaging of these tumors revealed a single
 continuous lesion. Postoperative histological examination revealed the presence of two distinct tumors, meningioma and glioblastoma
 multiforme. To elucidate the mechanism of synchronous tumor formation, we performed immunohistochemical analysis of the proteins
 involved in the receptor tyrosine kinase, Wnt, and Notch signaling pathways. These analyses showed that platelet-derived growth
 factor (PDGF) receptors-α and β were overexpressed in both tumors, thereby indicating the oncogenic effects of activated signaling
 of these receptors. The PDGF-mediated paracrine system may induce one tumor from ...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3168481</comments>
            <pubDate>Sun, 10 Jan 2010 06:44:46 +0100</pubDate>
            <guid isPermaLink="false">3168481</guid>        </item>
        <item>
            <title>Phase II trial of intratumoral BCNU injection and radiotherapy on untreated adult malignant glioma</title>
            <link>http://www.medworm.com/index.php?rid=3168482&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F3322753p12084p25%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;DTI-015 (BCNU dissolved in ethanol) utilizes solvent facilitated perfusion (SFP) for intratumoral drug delivery. A phase II
 clinical trial of DTI-015 and fractionated external beam radiotherapy on newly diagnosed, malignant gliomas investigated early
 changes in tumour physiology and metabolism, clinical outcome and safety. Pre- and post DTI-015 injection neuro-imaging included
 computed tomography (CT) cerebral blood flow and volume, glucose and thallium single photon emission computed tomography (SPECT)
 and magnetic resonance imaging (MRI). Clinical status was determined before and after DTI-015, prior to radiotherapy and 3&amp;nbsp;monthly
 thereafter until progression (defined by Macdonald criteria). Primary endpoint was radiographic response. Secondary endpoints
 wer...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3168482</comments>
            <pubDate>Sun, 10 Jan 2010 06:44:38 +0100</pubDate>
            <guid isPermaLink="false">3168482</guid>        </item>
        <item>
            <title>Expression of D2RmRNA isoforms and ERmRNA isoforms in prolactinomas: correlation with the response to bromocriptine and with tumor biological behavior</title>
            <link>http://www.medworm.com/index.php?rid=3160625&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F5t12788832010715%2F</link>
            <description>The objective
 of this study was to analyze the different expression of ERmRNA and D2RmRNA isoforms in prolactinomas responsive and resistant
 to dopamine agonist (DA), and to discuss the correlation of such gene expression with tumor biological behavior. A prospective
 study of 20 consecutive patients who harbored prolactinomas was designed. Patients were classified as responsive (14 cases)
 or resistant (six cases) according to their clinical and biochemical response to bromocriptine. Tumor tissue samples were
 examined by means of QRT–PCR analysis. Median D2SmRNA expression in responsive patients was about 2.5-fold that in resistant
 ones (13.5&amp;nbsp;±&amp;nbsp;10.4 and 5.4&amp;nbsp;±&amp;nbsp;2.4, respectively, P&amp;nbsp;=&amp;nbsp;0.09). No significant difference was found between D2LmRNA expression ...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3160625</comments>
            <pubDate>Fri, 08 Jan 2010 21:39:32 +0100</pubDate>
            <guid isPermaLink="false">3160625</guid>        </item>
        <item>
            <title>Vascular gene expression patterns are conserved in primary and metastatic brain tumors</title>
            <link>http://www.medworm.com/index.php?rid=3160626&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fc2n22566r7518m64%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Malignant primary glial and secondary metastatic brain tumors represent distinct pathological entities. Nevertheless, both
 tumor types induce profound angiogenic responses in the host brain microvasculature that promote tumor growth. We hypothesized
 that primary and metastatic tumors induce similar microvascular changes that could function as conserved angiogenesis based
 therapeutic targets. We previously isolated glioma endothelial marker genes (GEMs) that were selectively upregulated in the
 microvasculature of proliferating glioblastomas. We sought to determine whether these genes were similarly induced in the
 microvasculature of metastatic brain tumors. RT-PCR and quantitative RT-PCR were used to screen expression levels of 20 candidate
 GEMs in primary and meta...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3160626</comments>
            <pubDate>Fri, 08 Jan 2010 21:39:31 +0100</pubDate>
            <guid isPermaLink="false">3160626</guid>        </item>
        <item>
            <title>Phase II NCCTG trial of RT + irinotecan and adjuvant BCNU plus irinotecan for newly diagnosed GBM</title>
            <link>http://www.medworm.com/index.php?rid=3160627&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fu462801827721646%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Irinotecan has radiosensitizing effects and shows synergism with nitrosoureas. We performed a Phase II study of RT and irinotecan,
 followed by BCNU plus irinotecan in newly-diagnosed GBM. The MTD for patients receiving enzyme-inducing anticonvulsants (EIAC)
 was as follows: irinotecan 400&amp;nbsp;mg/m2/week on Days 1, 8, 22 and 29 during RT, followed by BCNU 100&amp;nbsp;mg/m2 Day 1, and irinotecan, 400&amp;nbsp;mg/m2 on Days 1, 8, 22 and 29, every 6&amp;nbsp;weeks. The MTD for non-EIAC patients was as follows: irinotecan 125&amp;nbsp;mg/m2/week on Days 1, 8, 22 and 29 during RT, followed by BCNU 100&amp;nbsp;mg/m2 Day 1 and irinotecan 75&amp;nbsp;mg/m2 Days 1, 8, 22 and 29, every 6&amp;nbsp;weeks. Median OS was 10.8 mos. (95% CI: 7.7–14.9); OS at 12&amp;nbsp;months was 44.6% (95% CI: 33.3–59.8)
 an...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3160627</comments>
            <pubDate>Fri, 08 Jan 2010 21:39:30 +0100</pubDate>
            <guid isPermaLink="false">3160627</guid>        </item>
        <item>
            <title>Up-front temozolomide in elderly patients with glioblastoma</title>
            <link>http://www.medworm.com/index.php?rid=3160628&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fw788n476r40604k3%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Upfront temozolomide (TMZ) is often proposed for elderly patients with malignant gliomas as an alternative to radiotherapy
 (RT). A recent randomized trial showed that RT provides a survival benefit in elderly glioblastoma patients (≥70&amp;nbsp;years) with
 good performance status (KPS&amp;nbsp;≥&amp;nbsp;70) compared with supportive care alone (median survival (MS)&amp;nbsp;=&amp;nbsp;29.1 vs. 16.9&amp;nbsp;weeks). We retrospectively
 analyzed all patients who were eligible for this trial, but who refused to participate and were finally treated with TMZ alone.
 Thirty-nine eligible patients (median age: 75&amp;nbsp;years (range 70–83), median KPS: 70 (range 70–80), histologically proven glioblastomas)
 were treated up-front with oral TMZ for 1–12 cycles (mean&amp;nbsp;=&amp;nbsp;5). One comple...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3160628</comments>
            <pubDate>Thu, 07 Jan 2010 22:22:13 +0100</pubDate>
            <guid isPermaLink="false">3160628</guid>        </item>
        <item>
            <title>Perfusion weighted magnetic resonance imaging to distinguish the recurrence of metastatic brain tumors from radiation necrosis after stereotactic radiosurgery</title>
            <link>http://www.medworm.com/index.php?rid=3160629&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fml7495015517p568%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;After stereotactic radiosurgery (SRS) for brain metastases, delayed radiation effects with mass effect may occur from several
 months to years later, when tumors may also recur. Aggressive salvage treatment would be beneficial for patients with recurrence,
 but may be contraindicated for those with dominant radiation effect. Conventional magnetic resonance (MR) imaging does not
 provide sufficient information to differentiate delayed radiation effects from tumor recurrence. Positron emission tomography,
 MR spectroscopy, and other modalities sometimes may lead to false findings of tumor recurrence. We prospectively applied perfusion
 MR imaging for the management strategy after SRS because it gives microvascular information about the lesions. Twenty-eight
 lesions were ...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3160629</comments>
            <pubDate>Thu, 07 Jan 2010 22:22:12 +0100</pubDate>
            <guid isPermaLink="false">3160629</guid>        </item>
        <item>
            <title>A case with coincidental diagnosis of primary central nervous system lymphoma and lymph node sarcoidosis</title>
            <link>http://www.medworm.com/index.php?rid=3154194&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fq9672g1m05751g85%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Primary central nervous system lymphoma (PCNSL) is rare. Clinical and histological differential diagnosis of systemic lymphoma
 and sarcoidosis continues to be a challenge. The first case report in the German and English literature of PCNSL and synchronous
 sarcoidosis is presented. Synchronous mediastinal lymphadenopathy suggestive of non-Hodgkin’s lymphoma (NHL) or sarcoidosis
 was noted. Both conditions require alternative therapeutic and prognostic considerations to PCNSL. A regime of intrathecal
 and adjuvant systemic chemotherapy led to transient clinical improvement prior to the patient’s demise through overwhelming
 sepsis and multiorgan failure. Post mortem findings confirmed synchronous PCNSL with mediastinal lymph node sarcoidosis.
 
	Content Type Journal...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3154194</comments>
            <pubDate>Wed, 06 Jan 2010 18:05:46 +0100</pubDate>
            <guid isPermaLink="false">3154194</guid>        </item>
        <item>
            <title>Cytogenetic analysis of paediatric astrocytoma using comparative genomic hybridisation and fluorescence in-situ hybridisation</title>
            <link>http://www.medworm.com/index.php?rid=3154195&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F2174782563k885p0%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Little is known about the cytogenetic and molecular genetic events that lead to the formation of paediatric astrocytoma. We
 have analysed 57 paediatric astrocytoma (WHO grades I–IV) using comparative genomic hybridisation in order to identify common
 regions of abnormality. Large regions of copy number alterations were infrequent with 71% of tumours demonstrating no genomic
 imbalance. Furthermore, the most frequent aberrations (including gain of 6q, 2q, and 7q, and loss of 16 and 12q) occurred
 in only a subset of cases. High-copy number amplification was seen in five tumours at 12 different regions. The presence of
 copy number alterations was significantly associated with increasing grade of malignancy, and gain of 12q and the presence
 of high-copy number amplifi...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3154195</comments>
            <pubDate>Wed, 06 Jan 2010 06:50:12 +0100</pubDate>
            <guid isPermaLink="false">3154195</guid>        </item>
        <item>
            <title>Erratum to: The role of stereotactic radiosurgery in the management of patients with newly diagnosed brain metastases: a systematic review and evidence-based clinical practice guideline</title>
            <link>http://www.medworm.com/index.php?rid=3136183&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F115231u4q62r8883%2F</link>
            <description>Content Type Journal ArticleCategory ErratumDOI 10.1007/s11060-009-0099-7Authors
		Mark E. Linskey, University of California-Irvine Medical Center Department of Neurosurgery Orange CA USADavid W. Andrews, Thomas Jefferson University Department of Neurosurgery Philadelphia PA USAAnthony L. Asher, Carolina Neurosurgery and Spine Associates Department of Neurosurgery Charlotte NC USAStuart H. Burri, Carolinas Medical Center Department of Radiation Oncology Charlotte NC USADouglas Kondziolka, University of Pittsburgh Medical Center Department of Neurological Surgery Pittsburgh PA USAPaula D. Robinson, McMaster University Evidence-based Practice Center Hamilton ON CanadaMario Ammirati, Ohio State University Medical Center Department of Neurosurgery Columbus OH USACharles S. Cobbs, California ...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3136183</comments>
            <pubDate>Thu, 31 Dec 2009 16:45:18 +0100</pubDate>
            <guid isPermaLink="false">3136183</guid>        </item>
        <item>
            <title>Prognostic factors in pediatric high-grade astrocytoma: the importance of accurate pathologic diagnosis</title>
            <link>http://www.medworm.com/index.php?rid=3134319&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F17431910l4073044%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;To characterize a population of pediatric high-grade astrocytoma (HGA) patients by confirming the proportion with a correct
 diagnosis, and determine prognostic factors for survival in a subset diagnosed with uniform pathologic criteria. Sixty-three
 children diagnosed with HGA were treated at the Johns Hopkins Hospital between 1977 and 2004. A single neuropathologist (P.C.B.)
 reviewed all available histologic samples (n&amp;nbsp;=&amp;nbsp;48). Log-rank analysis was used to compare survival by patient, tumor, and treatment factors. Median follow-up was 16&amp;nbsp;months
 for all patients and 155&amp;nbsp;months (minimum 54&amp;nbsp;months) for surviving patients. Median survival for all patients (n&amp;nbsp;=&amp;nbsp;63) was 14&amp;nbsp;months with 10 long-term survivors (survival &amp;gt;48&amp;nbsp;mont...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3134319</comments>
            <pubDate>Wed, 30 Dec 2009 16:45:25 +0100</pubDate>
            <guid isPermaLink="false">3134319</guid>        </item>
        <item>
            <title>Secondary fibrosarcoma of the brain stem treated with cyclophosphamide and Imatinib</title>
            <link>http://www.medworm.com/index.php?rid=3134318&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fh02gx1g6855k1437%2F</link>
            <description>We present
 the case of a 48-year old man with brainstem fibrosarcoma 20&amp;nbsp;years following radiation therapy received for a pituitary tumor.
 We discuss this case in the context of the diagnostic criteria for these tumors, and previous reports of secondary and primary
 sarcomas of the central nervous system.
 
	Content Type Journal ArticleCategory Case ReportDOI 10.1007/s11060-009-0096-xAuthors
		Daniela Alexandru, University of California, Irvine Department of Neurological Surgery Irvine CA USADenise K. Van Horn, Hoag Hospital Department of Pathology Newport Beach CA USADaniela Annenelie Bota, University of California, Irvine Department of Neurology Irvine CA 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=3134318</comments>
            <pubDate>Wed, 30 Dec 2009 16:45:25 +0100</pubDate>
            <guid isPermaLink="false">3134318</guid>        </item>
        <item>
            <title>Sarcoma metastatic to the brain: a series of 35 cases and considerations from 27 years of experience</title>
            <link>http://www.medworm.com/index.php?rid=3130560&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F60138122p153vjw1%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The authors report their 27-year experience regarding 35 cases of supratentorial brain metastasis from sarcoma treated in
 a single institution: these included ten osteosarcomas, seven leiomyosarcomas, five Ewing sarcomas, four malignant fibrous
 histiocytomas, three alveolar soft-part sarcomas (ASPS), two rhabdomyosarcomas, one liposarcoma, and three unclassified sarcomas.
 The first 15 cases of the series have already been described in a previous publication. Median survival after craniotomy was
 9.8&amp;nbsp;months (range: 4–24). In patients with preoperative Karnofsky performance score (KPS)&amp;nbsp;&amp;gt;&amp;nbsp;60 it was 12.8&amp;nbsp;months (range:
 6.5–24&amp;nbsp;months) versus 5.4&amp;nbsp;months for those patients with a KPS&amp;nbsp;≤&amp;nbsp;60 (P&amp;nbsp;=&amp;nbsp;0.01). Eight patients...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3130560</comments>
            <pubDate>Tue, 29 Dec 2009 06:54:44 +0100</pubDate>
            <guid isPermaLink="false">3130560</guid>        </item>
        <item>
            <title>Overexpression of septin 7 suppresses glioma cell growth</title>
            <link>http://www.medworm.com/index.php?rid=3122736&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fp21m236v3x23094q%2F</link>
            <description>This study is to further examine
 the expression of SEPT7 in glioma samples and characterizes its role on cell cycle progression and growth of glioma cells.
 mRNA and protein expression of SEPT7 were detected by RT-PCR, immunohistochemical staining, and western blot analysis in human
 glioma specimens and normal brain tissues. A pcDNA3-SEPT7 expression plasmid was constructed and transfected into human glioblastoma
 cell line U251, and cell proliferation and apoptosis were examined. The growth of established U251 and TJ905 subcutaneous
 xenograft gliomas was measured in nude mice treated with pcDNA3-SEPT7 and U251 xenograft tumors treated with SEPT7 siRNA.
 SEPT7 expression is negatively correlated with the increase of glioma grade. Overexpression of SEPT7 is able to inhibit cell
 prolifer...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3122736</comments>
            <pubDate>Fri, 25 Dec 2009 00:19:49 +0100</pubDate>
            <guid isPermaLink="false">3122736</guid>        </item>
        <item>
            <title>High rate of deletion of chromosomes 1p and 19q in insular oligodendroglial tumors</title>
            <link>http://www.medworm.com/index.php?rid=3122737&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fn077mt723p447h4w%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;It has been reported recently that oligodendroglial tumors arising in the insula rarely harbor co-deletions of chromosomes
 1p and 19q, a molecular signature which is associated with a good prognosis and increased responsiveness to radiation and
 chemotherapy compared with tumors in which 1p and/or 19q is intact. In the context of this claim, we analyzed a series of
 insular oligodendroglial tumors in order to determine the frequency of 1p/19q co-deletion in tumors arising in this region.
 We identified 14 insular cases operated on after 2003 in which testing for losses of 1p and 19q was performed. Of these cases,
 co-deletion of 1p and 19q occurred in eight (57%). Four (50%) of eight oligodendrogliomas and four (67%) of six oligoastrocytomas
 demonstrated 1p/19q co-del...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3122737</comments>
            <pubDate>Fri, 25 Dec 2009 00:19:48 +0100</pubDate>
            <guid isPermaLink="false">3122737</guid>        </item>
        <item>
            <title>Bevacizumab-induced diffusion-restricted lesions in malignant glioma patients</title>
            <link>http://www.medworm.com/index.php?rid=3122738&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fnp015175k778567j%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Bevacizumab is an anti-vascular endothelial growth factor (VEGF) antibody with activity against recurrent malignant glioma
 inducing high rates of objective responses as assessed by magnetic resonance imaging (MRI). However, the mechanisms of the
 anti-tumor action of bevacizumab are controversial. In particular, it is unclear whether and when bevacizumab induces hypoxia
 in gliomas. Vascular normalization with hyperperfusion and enhanced oxygen delivery to the tumor has been suggested as an
 alternative mechanism. We analyzed diffusion-weighted imaging (DWI) and apparent diffusion coefficient (ADC) maps in 18 consecutive
 patients with recurrent malignant glioma before and after exposure to bevacizumab. Stroke-like lesions with diffusion restriction
 on DWI and corresp...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3122738</comments>
            <pubDate>Fri, 25 Dec 2009 00:19:47 +0100</pubDate>
            <guid isPermaLink="false">3122738</guid>        </item>
        <item>
            <title>Parafalcine lesions in the cancer patient: diagnostic dilemma—meningioma or metastatic lesion?</title>
            <link>http://www.medworm.com/index.php?rid=3122739&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fytmm952024006378%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The authors present two cases that illustrate the difficulty in radiographically distinguishing between meningioma and metastatic
 lesions in patients with known cancer, especially with a parafalcine tumor location. The first patient with known metastatic
 prostate cancer had imaging studies suggestive of a parafalcine meningioma, but after surgical resection the lesion was found
 to be histologically consistent with metastatic disease. Conversely, the second patient was thought to have a metastatic breast
 cancer lesion in the parafalcine region. This presumptive diagnosis based on imaging findings led the patient to undergo radiosurgery
 treatment; however, the lesion grew over a several-month course and was eventually resected. The pathological analysis revealed
 tha...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3122739</comments>
            <pubDate>Thu, 24 Dec 2009 19:45:58 +0100</pubDate>
            <guid isPermaLink="false">3122739</guid>        </item>
        <item>
            <title>Transcranial electro-hyperthermia combined with alkylating chemotherapy in patients with relapsed high-grade gliomas: phase I clinical results</title>
            <link>http://www.medworm.com/index.php?rid=3121215&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fn45715524u271163%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Non-invasive loco-regional electro-hyperthermia (EHT) plus alkylating chemotherapy is occasionally used as salvage treatment
 in the relapse of patients with high-grade gliomas. Experimental data and retrospective studies suggest potential effects.
 However, no prospective clinical results are available. We performed a single-center prospective non-controlled single-arm
 Phase I trial. Main inclusion criteria were recurrent high-grade glioma WHO Grade III or IV, age 18–70, and Karnofsky performance
 score ≥70. Primary endpoints were dose-limiting toxicities (DLT) and maximum tolerated dose (MTD) with the combined regimen.
 Groups of 3 or 4 patients were treated 2–5 times a week in a dose-escalation scheme with EHT. Alkylating chemotherapy (ACNU,
 nimustin) was adm...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3121215</comments>
            <pubDate>Wed, 23 Dec 2009 22:36:24 +0100</pubDate>
            <guid isPermaLink="false">3121215</guid>        </item>
        <item>
            <title>Gli1 inhibition induces cell-cycle arrest and enhanced apoptosis in brain glioma cell lines</title>
            <link>http://www.medworm.com/index.php?rid=3105939&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fk75u05476hqv0p34%2F</link>
            <description>In conclusion, our findings support an important
 role of Gli1 in cell-cycle and apoptosis regulation in human brain gliomas; hence, it can serve as a potential target of new
 therapeutic strategies for these diseases.
 
	Content Type Journal ArticleCategory Laboratory Investigation - Human/Animal TissueDOI 10.1007/s11060-009-0082-3Authors
		Ke Wang, Huashan Hospital, Fudan University Department of Neurosurgery Shanghai 200040 ChinaLi Pan, Huashan Hospital, Fudan University Department of Neurosurgery Shanghai 200040 ChinaXiaoming Che, Huashan Hospital, Fudan University Department of Neurosurgery Shanghai 200040 ChinaDaming Cui, Huashan Hospital, Fudan University Department of Neurosurgery Shanghai 200040 ChinaChao Li, Huashan Hospital, Fudan University Department of Neuropathology Shanghai...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3105939</comments>
            <pubDate>Fri, 18 Dec 2009 16:08:23 +0100</pubDate>
            <guid isPermaLink="false">3105939</guid>        </item>
        <item>
            <title>Primary diffuse cerebral leptomeningeal atypical teratoid rhabdoid tumor: report of the first case</title>
            <link>http://www.medworm.com/index.php?rid=3105940&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fkt7866228557n663%2F</link>
            <description>In this report, we describe a very unusual case
 of a child who presented with signs and symptoms suggestive of leptomeningitis. However, imaging studies and histologic findings
 showed plaque-like AT/RT involving the leptomeninges of the cerebrum, cerebellum, and spinal cord. The disease proved to be
 rapidly fatal and resulted in the patient’s death within approximately two weeks. To our knowledge, this is the first case
 of primary leptomeningeal AT/RT involving the supratentorial leptomeninges.
 
	Content Type Journal ArticleCategory Case ReportDOI 10.1007/s11060-009-0094-zAuthors
		Bassem El-Nabbout, University of Arkansas for Medical Sciences and Arkansas Children’s Hospital Department of Neurology One children’s Way Little Rock AR 72202 USARolla Shbarou, University of Arkansas...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3105940</comments>
            <pubDate>Fri, 18 Dec 2009 07:22:40 +0100</pubDate>
            <guid isPermaLink="false">3105940</guid>        </item>
        <item>
            <title>Bevacizumab fails to treat temporal paraganglioma: discussion and case illustration</title>
            <link>http://www.medworm.com/index.php?rid=3105943&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fy512471xh6u6mw25%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Temporal paragangliomas are highly vascular tumors treated primarily by surgical resection. However, surgery to remove these
 tumors is associated with significant morbidity, including cranial nerve dysfunction. Interestingly, these tumors have been
 shown to express vascular endothelial growth factor (VEGF). A variety of tumors expressing VEGF and the VEGF receptor have
 been shown to reduce in size and vascularity when treated with the VEGF-specific antibody, bevacizumab (Avastin®). We hypothesized that paragangliomas may be treated noninvasively with bevacizumab, either as a primary treatment or as
 a useful adjuvant to surgical resection or radiation. Thus, our aim was to evaluate the effects of bevacizumab on this patient’s
 paraganglioma. A 36-year-old female p...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3105943</comments>
            <pubDate>Fri, 18 Dec 2009 07:10:04 +0100</pubDate>
            <guid isPermaLink="false">3105943</guid>        </item>
        <item>
            <title>Construction of a ganciclovir-sensitive lentiviral vector to assess the influence of angiopoietin-3 and soluble Tie2 on glioma growth</title>
            <link>http://www.medworm.com/index.php?rid=3105942&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fywup7520351m6140%2F</link>
            <description>This study also provides a lentiviral vector design for
 safer gene therapy.
 
	Content Type Journal ArticleCategory Laboratory Investigation - Human/Animal TissueDOI 10.1007/s11060-009-0095-yAuthors
		Marie-Josée Beaudet, Laval University Hospital Research Center Department of Endocrinology and Genomics 2705 Laurier Boulevard Quebec City QC G1V 4G2 CanadaNaika Rueda, Laval University Hospital Research Center Department of Endocrinology and Genomics 2705 Laurier Boulevard Quebec City QC G1V 4G2 CanadaGary P. Kobinger, Public Health Agency of Canada National Microbiology Laboratory Winnipeg MB CanadaJérôme Villeneuve, Laval University Hospital Research Center Department of Endocrinology and Genomics 2705 Laurier Boulevard Quebec City QC G1V 4G2 CanadaLuc Vallières, Laval University Hosp...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3105942</comments>
            <pubDate>Fri, 18 Dec 2009 07:10:04 +0100</pubDate>
            <guid isPermaLink="false">3105942</guid>        </item>
        <item>
            <title>Monotherapy with methotrexate for primary central nervous lymphoma has single agent activity in the absence of radiotherapy: a single institution cohort</title>
            <link>http://www.medworm.com/index.php?rid=3105941&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fq92096637w385p65%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;We have retrospectively reviewed toxicities and response of a cohort of primary central nervous system lymphoma (PCNSL) patients
 treated with high dose parenteral methotrexate (MTX) monotherapy without whole brain radiation. From The Massachusetts General
 Hospital (MGH) Cancer Registry, active since 1946, we selected all immunocompetent patients with histologic and/or radiographic
 PCNSL diagnosed between 1980 and 2007. We identified the recipients of MTX with leucovorin rescue as sole therapy. No patient
 received radiation therapy (XRT). We analyzed this cohort for toxicity, response and patterns of recurrence. The cohort of
 121 patients received on average 11 cycles of intravenous MTX at a median dose of 8&amp;nbsp;g/m2. Median interval between cycles was 10&amp;nbsp;days...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3105941</comments>
            <pubDate>Fri, 18 Dec 2009 07:10:04 +0100</pubDate>
            <guid isPermaLink="false">3105941</guid>        </item>
        <item>
            <title>Angiogenesis and expression of estrogen and progesterone receptors as predictive factors for recurrence of meningioma</title>
            <link>http://www.medworm.com/index.php?rid=3097670&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ff63781x1262111r4%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Meningiomas are benign tumors, with low rate of recurrence after surgery. The most important factor predicting recurrence
 is the extent of surgical resection; other factors have been studied with conflicting results. Angiogenesis, an important
 substratum for growth and spread of neoplasic cells, and the expression of estrogen and progesterone receptors (ER, PR), could
 play a role in the recurrence of meningioma. We evaluated 42 patients with meningioma diagnosis (confirmed by histopathology)
 treated exclusively by surgery between January 1995 and December 1999, and compared the recurring and non-recurring groups
 after a ten-year follow-up period. Recurrence was associated with several factors including vascular density (VD), cell proliferation
 index (CPI), ER, PR,...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3097670</comments>
            <pubDate>Tue, 15 Dec 2009 07:08:02 +0100</pubDate>
            <guid isPermaLink="false">3097670</guid>        </item>
        <item>
            <title>Meningeal carcinomatosis from penile squamous cell carcinoma</title>
            <link>http://www.medworm.com/index.php?rid=3097669&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F7j02t03514460676%2F</link>
            <description>We report herein a clinical case of a patient with meningeal carcinomatosis from penile squamous cell carcinoma. A 68-year-old
 man presented with mental changes, headaches, and unstable gait. Examinations revealed brain metastases and infiltration of
 the leptomeninges and subarachnoid space by carcinoma cells. Only 11&amp;nbsp;months earlier the patient had been diagnosed with penile
 squamous cell carcinoma of poor differentiation and had underwent subtotal penectomy and adjuvant chemotherapy and radiation.
 Infiltration of the central nervous system with penile cancer is extremely rare, and only five cases with brain metastases
 have been described to date. This is the first report of a patient with penile cancer spread to the leptomeninges.
 
	Content Type Journal ArticleCategory Case Rep...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3097669</comments>
            <pubDate>Tue, 15 Dec 2009 07:08:02 +0100</pubDate>
            <guid isPermaLink="false">3097669</guid>        </item>
        <item>
            <title>Central nervous system relapse continues to be a therapeutic challenge in extensive disease small-cell lung cancer patients with initial symptomatic brain metastases and good response to chemoradiotherapy</title>
            <link>http://www.medworm.com/index.php?rid=3097671&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fe771r61j17808251%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;A summary is presented of four case studies of extensive disease small-cell lung cancer patients with initial symptomatic
 brain metastases, who were initially successfully treated with concurrent chemoradiotherapy of the neurocranium followed by
 consolidation chemotherapy and thoracic chemoradiotherapy, but shortly after the initial treatment developed a sequence of
 central nervous system relapses despite second-line therapy. Symptoms of the effect on the central nervous system dominated
 the course of the cancer disease, whereas the primary tumor mass remained in complete remission in all four patients until
 the end of the follow-up period.
 
	Content Type Journal ArticleCategory Clinical Study - Patient StudyDOI 10.1007/s11060-009-0079-yAuthors
		Farkhad Manapov, ...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3097671</comments>
            <pubDate>Tue, 15 Dec 2009 07:08:00 +0100</pubDate>
            <guid isPermaLink="false">3097671</guid>        </item>
        <item>
            <title>Patterns of failure after stereotactic radiotherapy of intracranial meningioma</title>
            <link>http://www.medworm.com/index.php?rid=3090179&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fj08502831657163h%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The aim of this work is to evaluate patterns of failure in patients with recurrent meningioma after stereotactic radiotherapy.
 Of 411 patients with intracranial meningioma treated with radiotherapy at our institution, 22 patients with local tumor progression
 diagnosed by magnetic resonance imaging (MRI) after radiotherapy (RT) were identified and further investigated. The histologic
 grade of the meningiomas was World Health Organization (WHO) grade&amp;nbsp;I in 54.5%, WHO grade&amp;nbsp;II in 27.3%, and WHO grade&amp;nbsp;III in
 9.1% of cases. Fourteen patients had received fractionated stereotactic RT; five patients underwent intensity-modulated RT.
 The median total dose was 57.6&amp;nbsp;Gy at 1.8&amp;nbsp;Gy/fraction, five times weekly. Local recurrences were divided into the dosi...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3090179</comments>
            <pubDate>Sun, 13 Dec 2009 06:42:06 +0100</pubDate>
            <guid isPermaLink="false">3090179</guid>        </item>
        <item>
            <title>Prognostic value of immunohistochemical profile and response to high-dose methotrexate therapy in primary CNS lymphoma</title>
            <link>http://www.medworm.com/index.php?rid=3090180&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fh6t1jr24361472x4%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Several biomarkers have been identified as prognostic factors in primary central nervous system lymphoma (PCNSL). However,
 the correlation between the histogenetic origin of PCNSL and the response to therapy is still unclear. To elucidate the utility
 of immunophenotypic markers in predicting clinical outcomes, we investigated 27 immunocompetent patients with PCNSL treated
 with high-dose methotrexate therapy. Of the 27 patients, 25 received whole-brain radiotherapy after high-dose methotrexate.
 Immunostaining for CD5, CD10, BCL-6, and MUM-1 was used to determine the immunophenotypic profile of diffuse large B-cell
 lymphoma of PCNSL. We then evaluated whether immunophenotypic markers were associated with the response to therapy or patients’
 survival. The response ...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3090180</comments>
            <pubDate>Sun, 13 Dec 2009 06:42:04 +0100</pubDate>
            <guid isPermaLink="false">3090180</guid>        </item>
        <item>
            <title>Meningioma of the cerebellopontine angle in identical twins: a case report</title>
            <link>http://www.medworm.com/index.php?rid=3090181&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F21q1793745555607%2F</link>
            <description>We present identical twin sisters with meningiomas. The tumors were located at a similar, but not
 a common, position (the cerebellopontine angle) in both twins. Histologically, both tumors were diagnosed as meningothelial
 meningiomas with an angiomatous component. Immunohistochemically, the Ki-67 indices in the two cases were 1.0 and 1.1, and
 the p53 positive rates were 0.2 and 0.9. The specimens in both cases were reactive to neurofibromin 2 (NF2). A comparative
 genomic hybridization (CGH) assay revealed an aberration in the long arm of chromosome X, but no aberrations in the long arm
 of chromosome 22 in either case. These results strongly suggest that genetic aberrations other than NF2 are associated with tumorigenesis in some types of sporadic meningiomas.
 
	Content Type Journal A...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3090181</comments>
            <pubDate>Sat, 12 Dec 2009 14:18:15 +0100</pubDate>
            <guid isPermaLink="false">3090181</guid>        </item>
        <item>
            <title>Efficacy of intracerebral delivery of cisplatin in combination with photon irradiation for treatment of brain tumors</title>
            <link>http://www.medworm.com/index.php?rid=3090182&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F64574778136330un%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;We have evaluated the efficacy of intracerebral (i.c.) convection-enhanced delivery (CED) of cisplatin in combination with
 photon irradiation for the treatment of F98 glioma-bearing rats. One thousand glioma cells were stereotactically implanted
 into the brains of Fischer rats and 13&amp;nbsp;days later cisplatin (6&amp;nbsp;μg/20&amp;nbsp;μl) was administered i.c. by CED at a flow rate of 0.5&amp;nbsp;μl/min.
 On the following day the animals were irradiated with a single 15&amp;nbsp;Gy dose of X-rays, administered by a linear accelerator
 (LINAC) or 78.8&amp;nbsp;keV synchrotron X-rays at the European Synchrotron Radiation Facility (ESRF). Untreated controls had a mean
 survival time (MST)&amp;nbsp;±&amp;nbsp;standard error of 24&amp;nbsp;±&amp;nbsp;1&amp;nbsp;days compared to &amp;gt;59&amp;nbsp;±&amp;nbsp;13&amp;nbsp...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3090182</comments>
            <pubDate>Fri, 11 Dec 2009 06:53:02 +0100</pubDate>
            <guid isPermaLink="false">3090182</guid>        </item>
        <item>
            <title>Erwin G. Van Meir (ed): CNS cancer: Models, markers, prognostic factors, targets, and therapeutic approaches</title>
            <link>http://www.medworm.com/index.php?rid=3090183&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fw05809h3t1782595%2F</link>
            <description>Content Type Journal ArticleCategory Book ReviewDOI 10.1007/s11060-009-0088-xAuthors
		Paul Kleihues, University Hospital Department of Pathology 8091 Zurich Switzerland
	

	
		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=3090183</comments>
            <pubDate>Fri, 11 Dec 2009 06:53:01 +0100</pubDate>
            <guid isPermaLink="false">3090183</guid>        </item>
        <item>
            <title>Osteochondroma of the convexity: pathologic-neuroimaging correlates of a lesion that mimics high-grade meningioma</title>
            <link>http://www.medworm.com/index.php?rid=3090184&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fu7k165246450v51u%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Intracranial chondromas are uncommon benign lesions usually attached to dura and located over the convexity of the skull.
 Osteochondromas are even rarer and additionally contain a benign bony component. Both lesions are reportedly difficult to
 distinguish from meningiomas on pre-operative neuroimaging studies, although few detailed pathologic-neuroimaging correlation
 studies have appeared in the literature, particularly for intracranial osteochondromas. A 33-year-old woman with a 4-year
 history of headaches presented with recent onset of left-sided muscle spasms and weakness. Two days prior to admission to
 our hospital, neuroimaging studies had shown a large right convexity mass with unusual multifocal bright signal intensities
 throughout an otherwise isointense m...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3090184</comments>
            <pubDate>Thu, 10 Dec 2009 15:10:09 +0100</pubDate>
            <guid isPermaLink="false">3090184</guid>        </item>
        <item>
            <title>Desmoplastic infantile astrocytoma with benign histological phenotype and multiple intracranial localizations at presentation</title>
            <link>http://www.medworm.com/index.php?rid=3090185&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ft81551t876k146t6%2F</link>
            <description>We report the sixth, and first noninfantile,
 case of DIA/DIG with multifocal initial presentation.
 
	Content Type Journal ArticleCategory Case ReportDOI 10.1007/s11060-009-0075-2Authors
		E. Uro-Coste, Rangueil University Hospital Department of Pathology Toulouse FranceG. Ssi-Yan-Kai, Rangueil University Hospital Department of Pathology Toulouse FranceC. Guilbeau-Frugier, Rangueil University Hospital Department of Pathology Toulouse FranceS. Boetto, Purpan University Hospital Department of Neurosurgery Toulouse FranceA. I. Bertozzi, Children University Hospital Department of Haematology-Oncology Toulouse FranceA. Sevely, Purpan University Hospital Department of Radiology Toulouse FranceK. Lolmede, INSERM U858 Toulouse FranceM. B. Delisle, Rangueil University Hospital Department of Pathol...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3090185</comments>
            <pubDate>Thu, 10 Dec 2009 15:10:07 +0100</pubDate>
            <guid isPermaLink="false">3090185</guid>        </item>
        <item>
            <title>Spontaneous canine gliomas: overexpression of EGFR, PDGFRα and IGFBP2 demonstrated by tissue microarray immunophenotyping</title>
            <link>http://www.medworm.com/index.php?rid=3080331&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fy7631047xmm77110%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Fifty-seven spontaneous canine gliomas were histologically classified and graded using the latest World Health Organization
 (WHO 2007) criteria for classification of human gliomas. A total of 19 canine astrocytomas were classified as follows: grade
 IV (GBM) n&amp;nbsp;=&amp;nbsp;7; grade III n&amp;nbsp;=&amp;nbsp;5; and grade II, n&amp;nbsp;=&amp;nbsp;7. Thirty-eight oligodendrogliomas were classified as either grade III (anaplastic) n&amp;nbsp;=&amp;nbsp;35 or low grade II n&amp;nbsp;=&amp;nbsp;3. Tissue microarray (TMA) immunohistochemistry was used to evaluate tumor expression of EGFR, PDGFRa and IGFBP2, three
 key molecules of known pathophysiological importance in human gliomas. Findings were correlated with tumor classification
 and grade. Increased EGFR expression was demonstrated in 57% of GBMs, 40%...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3080331</comments>
            <pubDate>Fri, 04 Dec 2009 21:17:40 +0100</pubDate>
            <guid isPermaLink="false">3080331</guid>        </item>
        <item>
            <title>Phase II trial of erlotinib with temozolomide and radiation in patients with newly diagnosed glioblastoma multiforme</title>
            <link>http://www.medworm.com/index.php?rid=3064094&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fl467p704762u5541%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Approximately 40–50% of glioblastomas (GBM) overexpress epidermal growth factor receptor (EGFR). Erlotinib is a specific and
 potent EGFR tyrosine kinase inhibitor active against refractory GBM. Patients with non-small cell lung cancer and ≥grade 2
 erlotinib-induced rash have improved survival. This phase 2 study assessed the efficacy and safety of concurrent radiation
 therapy (RT) and temozolomide with pharmacodynamic dose escalation of erlotinib in patients with newly diagnosed GBM. Patients
 received RT 60&amp;nbsp;Gy in 30 fractions with concurrent temozolomide 75&amp;nbsp;mg/m2/day&amp;nbsp;×&amp;nbsp;42&amp;nbsp;days, followed in four weeks by temozolomide 150–200&amp;nbsp;mg/m2/day&amp;nbsp;×&amp;nbsp;5, every 28&amp;nbsp;days for 12 cycles. Patients received erlotinib, 50&amp;nbsp;mg/day and...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3064094</comments>
            <pubDate>Fri, 04 Dec 2009 07:20:01 +0100</pubDate>
            <guid isPermaLink="false">3064094</guid>        </item>
        <item>
            <title>The role of stereotactic radiosurgery in the management of patients with newly diagnosed brain metastases: a systematic review and evidence-based clinical practice guideline</title>
            <link>http://www.medworm.com/index.php?rid=3064095&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F7w84227x88442213%2F</link>
            <description>Abstract
 
 Question
 &amp;nbsp;&amp;nbsp;Should patients with newly-diagnosed metastatic brain tumors undergo stereotactic radiosurgery (SRS) compared with other treatment
 modalities?
 
 
 Target population
 
 
 
 
 These recommendations apply to adults with newly diagnosed solid brain metastases amenable to SRS; lesions amenable to SRS
 are typically defined as measuring less than 3&amp;nbsp;cm in maximum diameter and producing minimal (less than 1&amp;nbsp;cm of midline shift)
 mass effect.
 
 
 
 
 Recommendations
 
 
 
 
 
 SRS plus WBRT vs. WBRT alone
 
 
 
 
 
 Level 1 Single-dose SRS along with WBRT leads to significantly longer patient survival compared with WBRT alone for patients with
 single metastatic brain tumors who have a KPS&amp;nbsp;≥&amp;nbsp;70.
 
 
 
 
 Level 2 Single-dose SRS along with W...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3064095</comments>
            <pubDate>Thu, 03 Dec 2009 18:21:57 +0100</pubDate>
            <guid isPermaLink="false">3064095</guid>        </item>
        <item>
            <title>The role of surgical resection in the management of newly diagnosed brain metastases: a systematic review and evidence-based clinical practice guideline</title>
            <link>http://www.medworm.com/index.php?rid=3064096&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fe088515136888570%2F</link>
            <description>Abstract
 
 Question
 &amp;nbsp;&amp;nbsp;Should patients with newly-diagnosed metastatic brain tumors undergo open surgical resection versus whole brain radiation
 therapy (WBRT) and/or other treatment modalities such as radiosurgery, and in what clinical settings?
 
 
 Target population
 
 
 
 
 These recommendations apply to adults with a newly diagnosed single brain metastasis amenable to surgical resection.
 
 
 
 Recommendations
 
 
 
 
 
 Surgical resection plus WBRT versus surgical resection alone
 
 
 
 
 
 Level 1 Surgical resection followed by WBRT represents a superior treatment modality, in terms of improving tumor control at the
 original site of the metastasis and in the brain overall, when compared to surgical resection alone.
 
 
 
 
 Surgical resection plus WBRT versus SRS&amp;nbsp;...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3064096</comments>
            <pubDate>Thu, 03 Dec 2009 18:21:55 +0100</pubDate>
            <guid isPermaLink="false">3064096</guid>        </item>
        <item>
            <title>The role of chemotherapy in the management of newly diagnosed brain metastases: a systematic review and evidence-based clinical practice guideline</title>
            <link>http://www.medworm.com/index.php?rid=3064097&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fm42x58l615326720%2F</link>
            <description>Abstract
 Target population&amp;nbsp;&amp;nbsp;This recommendation applies to adults with newly diagnosed brain metastases; however, the recommendation below does not apply
 to the exquisitely chemosensitive tumors, such as germinomas metastatic to the brain.
 
 
 
 Recommendation&amp;nbsp;&amp;nbsp;
 Should patients with brain metastases receive chemotherapy in addition to whole brain radiotherapy (WBRT)?
 
 
 
 Level 1 Routine use of chemotherapy following WBRT for brain metastases has not been shown to increase survival and is not recommended.
 Four class I studies examined the role of carboplatin, chloroethylnitrosoureas, tegafur and temozolomide, and all resulted
 in no survival benefit. Two caveats are provided in order to allow the treating physician to individualize decision-making:
 First, the ma...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3064097</comments>
            <pubDate>Thu, 03 Dec 2009 18:21:54 +0100</pubDate>
            <guid isPermaLink="false">3064097</guid>        </item>
        <item>
            <title>The role of whole brain radiation therapy in the management of newly diagnosed brain metastases: a systematic review and evidence-based clinical practice guideline</title>
            <link>http://www.medworm.com/index.php?rid=3064098&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fv2k003021882774p%2F</link>
            <description>Abstract
 Should whole brain radiation therapy (WBRT) be used as the sole therapy in patients with newly-diagnosed, surgically accessible,
 single brain metastases, compared with WBRT plus surgical resection, and in what clinical settings?&amp;nbsp;&amp;nbsp;
 Target population
 
 
 This recommendation applies to adults with newly diagnosed single brain metastases amenable to surgical resection; however,
 the recommendation does not apply to relatively radiosensitive tumors histologies (i.e., small cell lung cancer, leukemia,
 lymphoma, germ cell tumors and multiple myeloma).
 
 
 
 
 Recommendation
 
 
 
 
 
 Surgical resection plus WBRT versus WBRT alone
 
 
 
 
 
 Level 1 Class I evidence supports the use of surgical resection plus post-operative WBRT, as compared to WBRT alone, in patients
 wi...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3064098</comments>
            <pubDate>Thu, 03 Dec 2009 18:21:53 +0100</pubDate>
            <guid isPermaLink="false">3064098</guid>        </item>
        <item>
            <title>Multiple sclerosis attacks triggered by hyperprolactinemia</title>
            <link>http://www.medworm.com/index.php?rid=3064099&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fm42866046j3033pt%2F</link>
            <description>We describe the case of a 32-year-old man affected
 by relapsing-remitting MS who experienced the first MS clinical event during the development of a prolactin-secreting adenoma
 and the only two MS relapses during adenoma recurrence. Prolactin may have facilitated the inflammatory process and triggered
 MS clinical attacks, suggesting a role of prolactin in immunomodulation and therefore in autoimmune disease course.
 
	Content Type Journal ArticleCategory Case ReportDOI 10.1007/s11060-009-0076-1Authors
		V. Nociti, Catholic University Institute of Neurology, Department of Neurosciences Largo Agostino Gemelli, 8 00168 Rome ItalyG. Frisullo, Catholic University Institute of Neurology, Department of Neurosciences Largo Agostino Gemelli, 8 00168 Rome ItalyT. Tartaglione, Catholic University ...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3064099</comments>
            <pubDate>Thu, 03 Dec 2009 12:50:12 +0100</pubDate>
            <guid isPermaLink="false">3064099</guid>        </item>
        <item>
            <title>The role of emerging and investigational therapies for metastatic brain tumors: a systematic review and evidence-based clinical practice guideline of selected topics</title>
            <link>http://www.medworm.com/index.php?rid=3064100&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fvw55868761322267%2F</link>
            <description>Abstract
 
 Question
 &amp;nbsp;&amp;nbsp;What evidence is available regarding the emerging and investigational therapies for the treatment of metastatic brain tumors?
 
 
 Target population
 
 
 
 
 These recommendations apply to adults with brain metastases.
 
 
 
 Recommendations
 
 
 
 
 
 New radiation sensitizers
 
 
 
 
 
 Level 2 A subgroup analysis of a large prospective randomized controlled trial (RCT) suggested a prolongation of time to neurological
 progression with the early use of motexafin-gadolinium (MGd). Nonetheless this was not borne out in the overall study population
 and therefore an unequivocal recommendation to use the currently available radiation sensitizers, motexafin-gadolinium and
 efaproxiral (RSR 13) cannot be provided.
 
 
 
 
 Interstitial modalities
 
 
 
 
 Ther...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3064100</comments>
            <pubDate>Thu, 03 Dec 2009 12:50:11 +0100</pubDate>
            <guid isPermaLink="false">3064100</guid>        </item>
        <item>
            <title>The role of steroids in the management of brain metastases: a systematic review and evidence-based clinical practice guideline</title>
            <link>http://www.medworm.com/index.php?rid=3064101&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fn11832031700653r%2F</link>
            <description>Discussion” and “Summary” section for additional details.
 
 
 
 
 
	Content Type Journal ArticleCategory Invited ManuscriptDOI 10.1007/s11060-009-0057-4Authors
		Timothy C. Ryken, Iowa Spine and Brain Institute Department of Neurosurgery Iowa City IA USAMichael McDermott, University of California San Francisco Department of Neurosurgery San Francisco CA USAPaula D. Robinson, McMaster University Evidence-Based Practice Centre Hamilton ON CanadaMario Ammirati, Ohio State University Medical Center Department of Neurosurgery Columbus OH USADavid W. Andrews, Thomas Jefferson University Department of Neurosurgery Philadelphia PA USAAnthony L. Asher, Carolina Neurosurgery and Spine Associates Department of Neurosurgery Charlotte NC USAStuart H. Burri, Carolinas Medical Center Department of...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3064101</comments>
            <pubDate>Wed, 02 Dec 2009 18:44:13 +0100</pubDate>
            <guid isPermaLink="false">3064101</guid>        </item>
        <item>
            <title>Evidence-linked, clinical practice guidelines—getting serious; getting professional</title>
            <link>http://www.medworm.com/index.php?rid=3064104&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fl91365558247u148%2F</link>
            <description>Content Type Journal ArticleCategory EditorialDOI 10.1007/s11060-009-0070-7Authors
		Mark E. Linskey, University of California Department of Neurological Surgery, UC Irvine Medical Center Bldg 56, Suite 400, 101 The City Drive South Orange CA 92868 USASteven N. Kalkanis, Henry Ford Health System Detroit MI 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=3064104</comments>
            <pubDate>Wed, 02 Dec 2009 18:44:11 +0100</pubDate>
            <guid isPermaLink="false">3064104</guid>        </item>
        <item>
            <title>The role of prophylactic anticonvulsants in the management of brain metastases: a systematic review and evidence-based clinical practice guideline</title>
            <link>http://www.medworm.com/index.php?rid=3064103&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fv69317g735r2381m%2F</link>
            <description>Abstract
 
 Question
 &amp;nbsp;&amp;nbsp;Do prophylactic anticonvulsants decrease the risk of seizure in patients with metastatic brain tumors compared with no treatment?
 
 
 Target population
 
 
 
 
 These recommendations apply to adults with solid brain metastases who have not experienced a seizure due to their metastatic
 brain disease.
 
 
 
 
 Recommendation
 
 
 
 
 
 Level 3 For adults with brain metastases who have not experienced a seizure due to their metastatic brain disease, routine prophylactic
 use of anticonvulsants is not recommended.
 
 
 
 Only a single underpowered randomized controlled trial (RCT), which did not detect a difference in seizure occurrence, provides
 evidence for decision-making purposes.
 
 
 
 
 
	Content Type Journal ArticleCategory Invited ManuscriptDOI 10....</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3064103</comments>
            <pubDate>Wed, 02 Dec 2009 18:44:11 +0100</pubDate>
            <guid isPermaLink="false">3064103</guid>        </item>
        <item>
            <title>Methodology used to develop the AANS/CNS management of brain metastases evidence-based clinical practice parameter guidelines</title>
            <link>http://www.medworm.com/index.php?rid=3064102&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fd842488756085422%2F</link>
            <description>Content Type Journal ArticleCategory Invited ManuscriptDOI 10.1007/s11060-009-0059-2Authors
		Paula D. Robinson, McMaster University Evidence-based Practice Center Hamilton ON CanadaSteven N. Kalkanis, Henry Ford Health System Department of Neurosurgery 2799 West Grand Blvd, K-11 Detroit MI 48202 USAMark E. Linskey, University of California-Irvine Medical Center Department of Neurosurgery Orange CA USAP. Lina Santaguida, McMaster University Evidence-based Practice Center Hamilton ON 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=3064102</comments>
            <pubDate>Wed, 02 Dec 2009 18:44:11 +0100</pubDate>
            <guid isPermaLink="false">3064102</guid>        </item>
        <item>
            <title>The role of retreatment in the management of recurrent/progressive brain metastases: a systematic review and evidence-based clinical practice guideline</title>
            <link>http://www.medworm.com/index.php?rid=3064105&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F4711x523t24123p7%2F</link>
            <description>Abstract
 
 Question
 &amp;nbsp;&amp;nbsp;
 What evidence is available regarding the use of whole brain radiation therapy (WBRT), stereotactic radiosurgery (SRS), surgical
 resection or chemotherapy for the treatment of recurrent/progressive brain metastases?
 
 
 
 Target population
 
 
 
 
 This recommendation applies to adults with recurrent/progressive brain metastases who have previously been treated with WBRT,
 surgical resection and/or radiosurgery. Recurrent/progressive brain metastases are defined as metastases that recur/progress
 anywhere in the brain (original and/or non-original sites) after initial therapy.
 
 
 
 
 Recommendation
 
 
 
 
 
 Level 3 Since there is insufficient evidence to make definitive treatment recommendations in patients with recurrent/progressive
 brain metastas...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3064105</comments>
            <pubDate>Wed, 02 Dec 2009 18:44:10 +0100</pubDate>
            <guid isPermaLink="false">3064105</guid>        </item>
        <item>
            <title>Evidence-based clinical practice parameter guidelines for the treatment of patients with metastatic brain tumors: introduction</title>
            <link>http://www.medworm.com/index.php?rid=3064106&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fu5v127351828308g%2F</link>
            <description>Content Type Journal ArticleCategory Invited ManuscriptDOI 10.1007/s11060-009-0065-4Authors
		Steven N. Kalkanis, Henry Ford Health System Department of Neurosurgery 2799 West Grand Blvd, K-11 Detroit MI 48202 USAMark E. Linskey, University of California-Irvine Medical Center Department of Neurosurgery Orange CA 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=3064106</comments>
            <pubDate>Wed, 02 Dec 2009 18:44:09 +0100</pubDate>
            <guid isPermaLink="false">3064106</guid>        </item>
        <item>
            <title>Adjuvant radiation therapy and chondroid chordoma subtype are associated with a lower tumor recurrence rate of cranial chordoma</title>
            <link>http://www.medworm.com/index.php?rid=3064107&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fn756166755h41806%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Cranial chordomas are rare tumors that have been difficult to study given their low prevalence. Individual case series with
 decades of data collection provide some insight into the pathobiology of this tumor and its responses to treatment. This meta-analysis
 is an attempt to aggregate the sum experiences and present a comprehensive review of their findings. We performed a comprehensive
 review of studies published in English language literature and found a total of over 2,000 patients treated for cranial chordoma.
 Patient information was then extracted from each paper and aggregated into a comprehensive database. The tumor recurrences
 in these patients were then stratified according to age (&amp;lt;21 vs. &amp;gt;21&amp;nbsp;years), histological findings (chondroid vs. typical)...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3064107</comments>
            <pubDate>Wed, 02 Dec 2009 08:36:07 +0100</pubDate>
            <guid isPermaLink="false">3064107</guid>        </item>
        <item>
            <title>Micro-RNA-128 (miRNA-128) down-regulation in glioblastoma targets ARP5 (ANGPTL6), Bmi-1 and E2F-3a, key regulators of brain cell proliferation</title>
            <link>http://www.medworm.com/index.php?rid=3040639&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fh516377r92363741%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;High density micro-RNA (miRNA) arrays, fluorescent-reporter miRNA assay and Northern miRNA dot-blot analysis show that a brain-enriched
 miRNA-128 is significantly down-regulated in glioblastoma multiforme (GBM) and in GBM cell lines when compared to age-matched
 controls. The down-regulation of miRNA-128 was found to inversely correlate with WHO tumor grade. Three bioinformatics-verified
 miRNA-128 targets, angiopoietin-related growth factor protein 5 (ARP5; ANGPTL6), a transcription suppressor that promotes
 stem cell renewal and inhibits the expression of known tumor suppressor genes involved in senescence and differentiation,
 Bmi-1, and a transcription factor critical for the control of cell-cycle progression, E2F-3a, were found to be up-regulated.
 Addition of exo...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3040639</comments>
            <pubDate>Thu, 26 Nov 2009 08:01:08 +0100</pubDate>
            <guid isPermaLink="false">3040639</guid>        </item>
        <item>
            <title>The expression level of sphingosine-1-phosphate receptor type 1 is related to MIB-1 labeling index and predicts survival of glioblastoma patients</title>
            <link>http://www.medworm.com/index.php?rid=3040640&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fav07u42q8817nkx5%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Although there are many reports on the clinical use of the MIB-1 labeling index (LI), which is a measure of proliferative
 activity in astrocytomas; its significance varies between studies. There are no known molecules that are directly linked to
 the MIB-1 LI in astrocytomas. We evaluated the clinical value of the MIB-1 LI in our human glioblastoma cases and determined
 the molecules that possibly influenced the MIB-1 LI. An immunohistochemical study of the MIB-1 protein was performed and MIB-1
 LIs of 38 glioblastomas were determined. In the same cases, epidermal growth factor receptor (EGFR), platelet-derived growth
 factor receptor-α (PDGFRA), and sphingosine-1-phosphate receptor type 1 (S1P1), which are known regulators of glioma cell proliferation, were detected ...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3040640</comments>
            <pubDate>Wed, 25 Nov 2009 16:51:28 +0100</pubDate>
            <guid isPermaLink="false">3040640</guid>        </item>
        <item>
            <title>BDNF mRNA expression is significantly upregulated in vestibular schwannomas and correlates with proliferative activity</title>
            <link>http://www.medworm.com/index.php?rid=3040641&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F945g2q1442367864%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The expression of neurotrophic factors, such as artemin, glial cell line-derived neurotrophic factor (GDNF), neurturin, transforming
 growth factors (TGF)-β1/β2 and brain-derived neurotrophic factor (BDNF), is enhanced in vestibular schwannomas compared to
 peripheral nerves. Furthermore, this upregulation may correlate with mitotic activity. Vestibular schwannoma arising from
 Schwann cells of the vestibular nerve are mostly benign and slow-growing. Most of the pathogenic mechanisms regulating the
 vestibular schwannoma growth process are unknown. An impaired growth regulation and imbalance between mitosis and apoptosis
 can be assumed. However, molecular mechanisms interfering with regulation of the vestibular schwannoma growth also modulated
 by mitogenic factors h...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3040641</comments>
            <pubDate>Wed, 25 Nov 2009 16:51:27 +0100</pubDate>
            <guid isPermaLink="false">3040641</guid>        </item>
        <item>
            <title>Antiepileptics in brain metastases: safety, efficacy and impact on life expectancy</title>
            <link>http://www.medworm.com/index.php?rid=3031635&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F141xu205382jl70w%2F</link>
            <description>In conclusion, regarding the use of newer antiepileptics in patients with seizures related to brain metastases,
 our data indicate that LEV, OXC and TPM significantly reduce seizure frequency (independently of systemic treatment), produce
 few side effects and appear not to affect life expectancy.
 
	Content Type Journal ArticleCategory Clinical Study - Patient StudyDOI 10.1007/s11060-009-0069-0Authors
		M. Maschio, National Institute for Cancer “Regina Elena” Center for Tumor-Related Epilepsy, Department of Neuroscience and Cervical-Facial Pathology Via Elio Chianesi 53 00144 Rome ItalyL. Dinapoli, National Institute for Cancer “Regina Elena” Center for Tumor-Related Epilepsy, Department of Neuroscience and Cervical-Facial Pathology Via Elio Chianesi 53 00144 Rome ItalyS. Gomellin...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3031635</comments>
            <pubDate>Tue, 24 Nov 2009 07:10:57 +0100</pubDate>
            <guid isPermaLink="false">3031635</guid>        </item>
        <item>
            <title>The cell-cycle kinetics of craniopharyngioma and its clinical significance</title>
            <link>http://www.medworm.com/index.php?rid=3031636&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fp07q42gh30363514%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Craniopharyngioma (CP) is a pathologically benign tumor with high incidence of recurrence and poor prognosis. DNA ploidy,
 S-phase fraction (SPF), and G2 phase/mitosis phase&amp;nbsp;+&amp;nbsp;S phase (G2/M&amp;nbsp;+&amp;nbsp;S) measured by flow cytometry (FCM) have been shown to
 correlate with cell cycle characteristics and clinical prognosis of other tumors. By use of FCM and terminal deoxynucleotide
 transferase-mediated dUTP nick end labeling (TUNEL) peroxidase, we compared DNA content, SPF, G2/M&amp;nbsp;+&amp;nbsp;S, necrosis and apoptosis
 in non-recurrent and recurrent tumor cells of CP from 63 cases including 32 adamantine epitheliomas (AEs) and 31 squamous
 papillary tumors (SPTs), and the ultrastructure of the CP cell was observed by transmission electron microscopy. Although
 no...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3031636</comments>
            <pubDate>Tue, 24 Nov 2009 07:10:55 +0100</pubDate>
            <guid isPermaLink="false">3031636</guid>        </item>
        <item>
            <title>Seizure risk in brain tumor patients with conversion to generic levetiracetam</title>
            <link>http://www.medworm.com/index.php?rid=3019948&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fp7742j71454827v8%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Breakthrough seizure activity has been reported with conversion from brand name to generic anticonvulsants. This has prompted
 several organizations to support physician notification of generic substitution and patient consent. Recently, a generic formulation
 of levetiracetam has become available. Risk of seizures with generic levetiracetam has yet to be reported. Literature was
 reviewed regarding risk of generic substitution. Four cases of seizure activity in primary brain tumor patients after conversion
 from Keppra to generic levetiracetam are reported. In all cases, there was no evidence of tumor growth or concurrent illness
 that would increase the risk of seizures. In three cases, the patients have remained seizure free with conversion back to
 Keppra. The final...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3019948</comments>
            <pubDate>Sat, 21 Nov 2009 08:50:57 +0100</pubDate>
            <guid isPermaLink="false">3019948</guid>        </item>
        <item>
            <title>High-dose chemotherapy and autologous stem cell rescue for atypical teratoid/rhabdoid tumor of the central nervous system</title>
            <link>http://www.medworm.com/index.php?rid=3019949&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fx02226h3163q426l%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp; Atypical Teratoid/Rhabdoid tumors (AT/RT) of the central nervous system are rare but aggressive tumors of childhood. Median
 survival with surgery and standard chemotherapy is less than 12&amp;nbsp;months. In an attempt to improve outcome, patients were treated
 with aggressive surgical resection and multi-agent chemotherapy, followed by high dose chemotherapy with autologous stem cell
 rescue. Nine consecutive children (median age 21&amp;nbsp;months) were diagnosed with AT/RT at the University of California San Francisco
 Childrens Hospital from 1997 to 2007 and treated with this aggressive approach. Diagnosis was confirmed using molecular markers.
 There are two long-term survivors (78 and 98&amp;nbsp;months from diagnosis). One additional patient is alive with disease. Three pa...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3019949</comments>
            <pubDate>Sat, 21 Nov 2009 08:50:55 +0100</pubDate>
            <guid isPermaLink="false">3019949</guid>        </item>
        <item>
            <title>Treatment of atypical central neurocytoma in a child with high dose chemotherapy and autologous stem cell rescue</title>
            <link>http://www.medworm.com/index.php?rid=3016030&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F12510351836g566h%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The authors describe a 9&amp;nbsp;month old female with recurrent atypical central neurocytoma and leptomeningeal spread treated with
 high dose chemotherapy, autologous stem cell rescue, and adjuvant therapy. She had a complete response to therapy and was
 disease free at 4&amp;nbsp;years of age until a recurrence 6&amp;nbsp;months later. The use of intensive chemotherapy followed by autologous
 stem cell rescue for atypical neurocytoma may be considered as an adjunct to surgical therapy in young patients with atypical
 neurocytoma not amenable to radiation therapy.
 
	Content Type Journal ArticleCategory Case ReportDOI 10.1007/s11060-009-0029-8Authors
		David Buchbinder, Children’s Hospital of Orange County Department of Pediatric Hematology 455 S. Main Street Orange CA 92868 U...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3016030</comments>
            <pubDate>Thu, 19 Nov 2009 07:50:11 +0100</pubDate>
            <guid isPermaLink="false">3016030</guid>        </item>
        <item>
            <title>Advanced adult esthesioneuroblastoma successfully treated with cisplatin and etoposide alternated with doxorubicin, ifosfamide and vincristine</title>
            <link>http://www.medworm.com/index.php?rid=3016031&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fb002710qj9w64770%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The esthesioneuroblastoma is a rare neuroendocrine tumor that derives from the olfactory cells. In the last 20&amp;nbsp;years, around
 1,000 cases have been described, with an overall survival rate of 60–70% at 5&amp;nbsp;years. The most common symptoms are nasal bleeding,
 nasal clogging and, in locally advanced cases, signs/symptoms of intracranic hypertension such as papilla edema, cefalea,
 and vomiting. The standard treatments are surgery and radiotherapy. Chemotherapy can be used in an adjuvant/neoadjuvant setting
 and in the metastatic phase, even if its role is still not established with certainty. Here, the case is reported of a young
 man (38&amp;nbsp;years old) with a locally advanced esthesioneuroblastoma. Two months before coming to our clinic, he had been treated
 e...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3016031</comments>
            <pubDate>Wed, 18 Nov 2009 19:20:34 +0100</pubDate>
            <guid isPermaLink="false">3016031</guid>        </item>
        <item>
            <title>Tissue factor mediates the HGF/Met-induced anti-apoptotic pathway in DAOY medulloblastoma cells</title>
            <link>http://www.medworm.com/index.php?rid=3009554&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F12u5556185w861k6%2F</link>
            <description>In this study, we report that stimulation of DAOY with HGF resulted in the protection of these cells against etoposide-induced
 apoptosis, this anti-apoptotic effect being correlated with an increase in the expression of tissue factor (TF), the initiator
 of the extrinsic pathway of coagulation. HGF-mediated protection from apoptosis was abolished by a c-Met inhibitor as well
 as by siRNA-mediated reduction of TF levels, implying a central role of Met-dependent induction of TF expression in this process.
 Accordingly, stimulation of DAOY with FVIIa, the physiological ligand of TF, also resulted in a significant protection from
 etoposide-mediated cytotoxicity. Overall, our results suggest the participation of the haemostatic system to drug resistance
 in MB and may thus provide novel thera...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3009554</comments>
            <pubDate>Wed, 18 Nov 2009 09:29:41 +0100</pubDate>
            <guid isPermaLink="false">3009554</guid>        </item>
        <item>
            <title>Imatinib mesylate (Glivec) inhibits Schwann cell viability and reduces the size of human plexiform neurofibroma in a xenograft model</title>
            <link>http://www.medworm.com/index.php?rid=3009555&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F325r15p5150p4286%2F</link>
            <description>In this study, we examined the effect of imatinib mesylate, a receptor
 tyrosine kinase inhibitor, on PNF-derived Schwann cells and PNF tumour growth in&amp;nbsp;vitro and in&amp;nbsp;vivo. In&amp;nbsp;vitro, PNF-derived
 primary Schwann cells express platelet-derived growth factors receptors (PDGFR) α and β, both targets of imatinib, and cell
 viability was reduced by imatinib mesylate, with 50% inhibition concentration (IC50) of 10&amp;nbsp;μM. For in&amp;nbsp;vivo studies, PNF tumour fragments xenografted onto the sciatic nerve of athymic nude mice were first characterized.
 The tumours persisted for at least 63&amp;nbsp;days and maintained typical characteristics of PNFs such as complex cellular composition,
 low proliferation rate and angiogenesis. A transient enlargement of the graft size was due to infl...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3009555</comments>
            <pubDate>Wed, 18 Nov 2009 05:13:17 +0100</pubDate>
            <guid isPermaLink="false">3009555</guid>        </item>
        <item>
            <title>Clinical and biological significance of forkhead class box O 3a expression in glioma: mediation of glioma malignancy by transcriptional regulation of p27kip1</title>
            <link>http://www.medworm.com/index.php?rid=2993167&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F31061329qt66gt46%2F</link>
            <description>In this study we investigated the status of
 FOXO3a expression and related signaling in human glioma in order to test its potential value as a therapeutic target for this
 disease. Immunohistochemistry, western blot, RT-PCR, and immunofluorescence staining analysis were performed on specimens
 from 70 cases of human glioma and on U87MG and T98G glioma cells. Our data showed FOXO3a expression is directly correlated
 with the malignant grade of glioma. More importantly, low expression of FOXO3a was associated with poor patient outcome. In
 vitro, FOXO3a modulated the cell cycle by transcriptional regulation of p27kip1. Administration of the PI3K pharmacological inhibitor LY294002 abrogated this effect by regulating FOXO3a expression and
 subcellular localization. Our results suggested that F...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2993167</comments>
            <pubDate>Fri, 13 Nov 2009 07:26:19 +0100</pubDate>
            <guid isPermaLink="false">2993167</guid>        </item>
        <item>
            <title>p53 regulates LIF expression in human medulloblastoma cells</title>
            <link>http://www.medworm.com/index.php?rid=2990234&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fe223p7360162w606%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Medulloblastomas are highly malignant, poorly differentiated childhood tumours arising in the cerebellum. These tumors rarely
 lose TP53, which is the most commonly mutated gene in cancer. Recent work has shown that the basal level of p53 plays an important
 role in maternal reproduction by maintaining the expression of LIF in the uterus. Since LIF can maintain the undifferentiated
 state of stem cells we set out to ask if p53 regulates LIF in the human medulloblastoma cell lines DAOY and D283MED. We also
 used p53−/− and p53+/+&amp;nbsp;isogenic HCT116 colorectal carcinoma cell lines, already reported to exhibit p53-dependent expression
 of the LIF D transcript, to establish the extent of p53-dependency for LIF M and T alternative transcripts. Whilst all three
 known, ...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2990234</comments>
            <pubDate>Thu, 12 Nov 2009 07:18:52 +0100</pubDate>
            <guid isPermaLink="false">2990234</guid>        </item>
        <item>
            <title>Adjuvant Gamma Knife radiosurgery following surgical resection of brain metastases: a 9-year retrospective cohort study</title>
            <link>http://www.medworm.com/index.php?rid=2986124&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fm1162h5155750653%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Given the potential morbidity of whole brain radiation therapy (WBRT), there has been an increasing trend to defer WBRT and
 deliver Gamma Knife stereotactic radiosurgery (GKS) to cerebral metastatic lesions. We analyzed our experience delivering
 GKS to the tumor cavity following surgical resection of brain metastases and compared our results to patients receiving WBRT
 after surgical resection of a metastatic lesion. We performed a retrospective review of patients undergoing surgical resection
 of at least one brain metastasis between December 1999 and December 2008. Both univariate and multivariate Cox proportional
 hazards regression were utilized to analyze the influence of various prognostic factors on survival. Twenty-five patients
 had a metastatic lesion resect...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2986124</comments>
            <pubDate>Wed, 11 Nov 2009 06:57:31 +0100</pubDate>
            <guid isPermaLink="false">2986124</guid>        </item>
        <item>
            <title>A surgically treated case of Lhermitte–Duclos disease with a precise natural history and high uptake of FDG on PET</title>
            <link>http://www.medworm.com/index.php?rid=2986123&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F6475567402527411%2F</link>
            <description>We describe herein a surgically treated case of Lhermitte–Duclos disease in a 33-year-old man. The clinical presentation seemed
 typical in terms of symptoms, neurological signs, and neuroimaging. High and heterogenous fluorodeoxyglucose uptake in positron
 emission tomography study is presented and discussed. Furthermore, we performed volumetric analysis of the tumor with sequential
 magnetic resonance imaging over the course of 7&amp;nbsp;years before surgery, making this report the first with a long-term natural
 history, revealing that this rare disease entity may have a neoplastic nature.
 
	Content Type Journal ArticleCategory Case ReportDOI 10.1007/s11060-009-0042-yAuthors
		Yuko Goto, Osaka University Graduate School of Medicine Department of Neurosurgery Yamadaoka 2-2, E6 Suita Osak...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2986123</comments>
            <pubDate>Wed, 11 Nov 2009 06:57:31 +0100</pubDate>
            <guid isPermaLink="false">2986123</guid>        </item>
        <item>
            <title>Involvement of osteopontin as a core protein in craniopharyngioma calcification formation</title>
            <link>http://www.medworm.com/index.php?rid=2982350&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fb497622274712886%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Matrix proteins are considered to be essential for biomineralization and to be important factors in cranioharyngioma calcification.
 Osteopontin (OPN) is a noncollagenous, acidic bone-matrix glycoprotein, which binds tightly to hydroxyapatite and appears
 to form an integral part of the mineralized matrix, probably important to the integrity of cell–matrix interactions. OPN is
 also a ligand for a cell membrane receptor, CD44v6, which is required for efficient OPN binding. To investigate the role of
 OPN in craniopharyngioma calcification formation, we studied the involvement of OPN and CD44v6 in craniopharyngiomas. Immunohistochemical
 staining was used in human craniopharyngiomas to detect the relationship of OPN and degree of calcification, and immunogold
 localiza...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2982350</comments>
            <pubDate>Tue, 10 Nov 2009 08:09:44 +0100</pubDate>
            <guid isPermaLink="false">2982350</guid>        </item>
        <item>
            <title>A case of primary leptomeningeal gliomatosis confined to the spinal cord</title>
            <link>http://www.medworm.com/index.php?rid=2974706&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F0137843864g4j346%2F</link>
            <description>We report a case of primary leptomeningeal gliomatosis limited to the spinal cord occurring in a 52&amp;nbsp;years-old patient, who
 presented with back pain and leg weakness. MRI-scan of the craniospinal axis revealed an enhancing cervicothoracic lesion
 confined to the leptomeninges. A diagnostic biopsy was taken followed by a six level cervicothoracic laminoplasty with the
 aim of debulking of the dorsal portion of the tumour and relieving cord compression. Two weeks following surgery, the patient
 developed bilateral arm weakness. Repeat imaging revealed extension of the lesion to the level of the lower medulla. This
 patient underwent spinal radiotherapy and concomitant chemotherapy with Temozolomide, but she died of pneumonia 8.5&amp;nbsp;months
 after the time of diagnosis. No post-mortem w...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2974706</comments>
            <pubDate>Sat, 07 Nov 2009 19:14:01 +0100</pubDate>
            <guid isPermaLink="false">2974706</guid>        </item>
        <item>
            <title>Primary spinal cord glioma: a Surveillance, Epidemiology, and End Results database study</title>
            <link>http://www.medworm.com/index.php?rid=2974707&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F7624132h1854406j%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;To characterize the overall survival (OS) and cause specific survival (CSS), and variables affecting outcome, in patients
 with primary spinal cord astrocytoma (SCA) and ependymoma (SCE). About 664 patients with SCA and 1,057 patients with SCE were
 analyzed using the Surveillance, Epidemiology, and End Results database. For grade 1, 2, 3 and 4 SCA, the 5-year OS was 82,
 70, 28 and 14%; the 5-year CSS was 89, 77, 36 and 20%. For SCA, lower grade, younger age, and undergoing resection significantly
 improved OS and CSS; treatment without radiotherapy was favorable for CSS. Smaller tumor size also improved survival. For
 grade 1, 2, and 3 SCE, the 5-year OS was 92, 97 and 58%; the 5-year CSS was 100, 98 and 64%. For SCE, lower grade, younger
 age, and undergoing resectio...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2974707</comments>
            <pubDate>Sat, 07 Nov 2009 07:44:59 +0100</pubDate>
            <guid isPermaLink="false">2974707</guid>        </item>
        <item>
            <title>Multiple extracranial metastases from secondary glioblastoma multiforme: a case report and review of the literature</title>
            <link>http://www.medworm.com/index.php?rid=2974708&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fn32607m373340186%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Extracranial metastasis of glioblastoma multiforme (GBM) is very rare, in spite of very aggressive tumor behavior and being
 documented in only a few patients. In this article we present a 25-year-old man with secondary glioblastoma associated with
 extracranial progression and distant metastasis. He was diagnosed by magnetic resononce (MR) with an intracranial lesion in
 the right parietofrontal region, which was subsequently resected. Histology revealed a diffuse astrocytoma (grade II). The
 tumor recurred 1&amp;nbsp;year later and the patient received a second craniotomy. A diagnosis of GBM was made. After radiotherapy,
 he presented with right cervical lymph node metastases. The cytomorphological features supported a diagnosis of metastatic
 glioblastoma multiforme. The...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2974708</comments>
            <pubDate>Sat, 07 Nov 2009 07:44:58 +0100</pubDate>
            <guid isPermaLink="false">2974708</guid>        </item>
        <item>
            <title>Lenalidomide stops progression of multifocal epithelioid hemangioendothelioma including intracranial disease</title>
            <link>http://www.medworm.com/index.php?rid=2974709&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fw8n7ux2624104322%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Epithelioid Hemangioendothelioma (EH) is a rare soft-tissue tumor which may present as an isolated tumor or can spread to
 affect internal organs. The course of EH varies, based on the tissue of origin. This case report describes a young woman who
 developed cutaneous EH with concurrent intracranial disease during pregnancy. After resection, the lesions returned. Even
 after several courses of chemotherapy and radiotherapy, the patient developed multifocal disease including pulmonary, skeletal,
 and liver disease. She now exhibits stable disease after approximately 6 years of therapy with lenalidomide.
 
	Content Type Journal ArticleCategory Case ReportDOI 10.1007/s11060-009-0017-zAuthors
		Ashley Sumrall, University of Mississippi Medical Center Department of Oncology ...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2974709</comments>
            <pubDate>Sat, 07 Nov 2009 07:44:55 +0100</pubDate>
            <guid isPermaLink="false">2974709</guid>        </item>
        <item>
            <title>Convection-enhanced delivery of free gadolinium with the recombinant immunotoxin MR1-1</title>
            <link>http://www.medworm.com/index.php?rid=2974710&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fm10k3lk248701251%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;A major obstacle in glioblastoma (GBM) therapy is the restrictive nature of the blood-brain barrier (BBB). Convection-enhanced
 delivery (CED) is a novel method of drug administration which allows direct parenchymal infusion of therapeutics, bypassing
 the BBB. MR1-1 is a novel recombinant immunotoxin that targets the GBM tumor-specific antigen EGFRvIII and can be delivered
 via CED infusion. However, drug distribution via CED varies dramatically, which necessitates active monitoring. Gadolinium
 conjugated to diethylenetriamine penta-acetic acid (Gd-DTPA) is a commonly used MRI contrast agent which can be co-infused
 with therapies using CED and may be useful in monitoring infusion leak and early distribution. Forty immunocompetent rats
 were implanted with intracerebr...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2974710</comments>
            <pubDate>Sat, 07 Nov 2009 07:44:53 +0100</pubDate>
            <guid isPermaLink="false">2974710</guid>        </item>
        <item>
            <title>Immunohistochemical detection of somatostatin receptor subtype 5 (SSTR-5) in cushing adenoma</title>
            <link>http://www.medworm.com/index.php?rid=2971438&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fl89m14244678377g%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorDOI 10.1007/s11060-009-0048-5Authors
		Wael Hassaneen, The University of Texas, M. D. Anderson Cancer Center Houston TX USADaniel P. Cahill, The University of Texas, M. D. Anderson Cancer Center Houston TX USAGregory N. Fuller, The University of Texas, M. D. Anderson Cancer Center Houston TX USANicholas B. Levine, The University of Texas, M. D. Anderson Cancer Center Houston TX 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=2971438</comments>
            <pubDate>Fri, 06 Nov 2009 06:53:27 +0100</pubDate>
            <guid isPermaLink="false">2971438</guid>        </item>
        <item>
            <title>Compartmental intrathecal radioimmunotherapy: results for treatment for metastatic CNS neuroblastoma</title>
            <link>http://www.medworm.com/index.php?rid=2968541&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fp07804022q60v008%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Innovation in the management of brain metastases is needed. We evaluated the addition of compartmental intrathecal antibody-based
 radioimmunotherapy (cRIT) in patients with recurrent metastatic central nervous system (CNS) neuroblastoma following surgery,
 craniospinal irradiation, and chemotherapy. Twenty one patients treated for recurrent neuroblastoma metastatic to the CNS,
 received a cRIT-containing salvage regimen incorporating intrathecal 131I-monoclonal antibodies (MoAbs) targeting GD2 or B7H3 following surgery and radiation. Most patients also received outpatient
 craniospinal irradiation, 3F8/GMCSF immunotherapy, 13-cis-retinoic acid and oral temozolomide for systemic control. Seventeen of 21&amp;nbsp;cRIT-salvage patients are alive 7–74&amp;nbsp;months (median
 33...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2968541</comments>
            <pubDate>Thu, 05 Nov 2009 07:58:51 +0100</pubDate>
            <guid isPermaLink="false">2968541</guid>        </item>
        <item>
            <title>Intrathecal liposomal cytarabine in combination with temozolomide in low-grade oligoastrocytoma with leptomeningeal dissemination</title>
            <link>http://www.medworm.com/index.php?rid=2947837&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fh64x08156275rh71%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Leptomeningeal dissemination of low-grade gliomas is an uncommon event. A 43-year old male presented with dizziness, gait
 ataxia, and diplopia. A nonenhancing lesion in the right cerebellar peduncle was identified, subtotally resected, and diagnosed
 as a grade II astrocytoma. After one year a nodular spread in the brain and leptomeninges was diagnosed, so the patient started
 chemotherapy with temozolomide and liposomal cytarabine. Complete remission was achieved after 12&amp;nbsp;months of treatment and
 the patient is still free from the disease after a follow-up of 24&amp;nbsp;months. We suggest that this combination may be a valuable
 treatment option.
 
	Content Type Journal ArticleCategory Case ReportDOI 10.1007/s11060-009-0040-0Authors
		Maria Grazia Passarin, USSL 22 ...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2947837</comments>
            <pubDate>Fri, 30 Oct 2009 07:49:38 +0100</pubDate>
            <guid isPermaLink="false">2947837</guid>        </item>
        <item>
            <title>Specific chromosomal imbalances as detected by array CGH in ependymomas in association with tumor location, histological subtype and grade</title>
            <link>http://www.medworm.com/index.php?rid=2944877&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F6830w2u50v505484%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Ependymomas are glial neoplasms originating from the wall of the ventricles or from the spinal canal. The significance of
 histopathological features in accurately predicting biological behavior is still debated. Moreover, key molecular events in
 the pathogenesis of ependymoma are yet to be defined. The main objective of the present study was to identify specific patterns
 of chromosomal aberrations that correlate with tumor location, histological subtype and grade. Forty-five ependymoma samples
 were analyzed by 1-megabase resolution array comparative genomic hybridization (CGH). Association between clinical or histopathological
 parameters and the genomic alterations identified was evaluated. The most frequently detected chromosome (chr) abnormalities
 were gain of c...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2944877</comments>
            <pubDate>Thu, 29 Oct 2009 07:22:22 +0100</pubDate>
            <guid isPermaLink="false">2944877</guid>        </item>
        <item>
            <title>MK886-induced apoptosis depends on the 5-LO expression level in human malignant glioma cells</title>
            <link>http://www.medworm.com/index.php?rid=2940763&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fm3k24728084848x5%2F</link>
            <description>In this study, we analyzed the effects of a 5-LO inhibitor, which inhibits the conversion of arachidonic
 acid to leukotrienes, on cell proliferation and apoptosis in human malignant glioma cells, including 5-LO-expressing cells
 U-87MG, A172 and 5-LO non-expressing cell U373. Growth of U-87MG and A172 cells, but not that of U373 cells, was inhibited
 in a dose-dependent manner by treatment with MK886. Similarly, specific 5-LO silencing by small interfering RNA reduced the
 growth of U-87MG and A172 cells. MK886 treatment reduced 5-LO activity independently of 5-LO-activating protein (FLAP) in
 human malignant glioma cells. MK886 treatment also induced cell apoptosis, measured by DNA fragmentation and nuclear condensation,
 in U-87MG and A172 cells but there were no signs in U373 cells. Mo...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2940763</comments>
            <pubDate>Wed, 28 Oct 2009 07:16:00 +0100</pubDate>
            <guid isPermaLink="false">2940763</guid>        </item>
        <item>
            <title>Imaging response criteria for recurrent gliomas treated with bevacizumab: Role of diffusion weighted imaging as an imaging biomarker</title>
            <link>http://www.medworm.com/index.php?rid=2936066&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F4938685676217400%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The purpose of this study was to assess the usefulness of diffusion weighted imaging as an additional imaging biomarker for
 treatment response in recurrent/progressive malignant gliomas treated with bevacizumab alone or in combination with other
 chemotherapeutic agents. Twenty patients treated with bevacizumab alone or concurrent chemotherapy were followed up with serial
 MR imaging. Volume and ADC values of contrast enhancing lesion (CELvol, CELADC) and also of non-enhancing lesion (NELvol, NELADC) were obtained. CELvol showed a progressive decrease in non-progressors with a median percentage change of −73.2% (P&amp;nbsp;=&amp;nbsp;0.001) as compared to −33.4% for progressors by 1 year/last imaging (P&amp;nbsp;=&amp;nbsp;0.382). NELvol also showed a decrease in non-progressors o...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2936066</comments>
            <pubDate>Mon, 26 Oct 2009 18:09:12 +0100</pubDate>
            <guid isPermaLink="false">2936066</guid>        </item>
        <item>
            <title>Hepatocyte growth factor in cerebrospinal fluid is associated with mortality and recurrence of glioblastoma, and could be of prognostic value</title>
            <link>http://www.medworm.com/index.php?rid=2928292&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F66qt5v02833842vn%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Malignant gliomas—glioblastoma multiforme and anaplastic astrocytoma—are among the most fatal forms of cancer in humans. It
 has been suggested that hepatocyte growth factor (HGF) is a reliable predictor of glioma malignancy; amounts of HGF are directly
 related to cellular proliferation, angiogenesis, low apoptotic rate, and poor prognosis (WHO III and IV). We measured the
 HGF content of cerebrospinal fluid (CSF) from patients with malignant glioma glioblastoma multiforme (WHO IV; n&amp;nbsp;=&amp;nbsp;14), anaplastic astrocytoma (WHO III; n&amp;nbsp;=&amp;nbsp;4), and meningioma (WHO I; n&amp;nbsp;=&amp;nbsp;9), and from control subjects (n&amp;nbsp;=&amp;nbsp;25), and found a high concentration of HGF in patients with malignant glioma. However, CSF concentrations from glioblastoma
 multiforme ...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2928292</comments>
            <pubDate>Sun, 25 Oct 2009 06:59:10 +0100</pubDate>
            <guid isPermaLink="false">2928292</guid>        </item>
        <item>
            <title>Activated EGFR signaling increases proliferation, survival, and migration and blocks neuronal differentiation in post-natal neural stem cells</title>
            <link>http://www.medworm.com/index.php?rid=2928293&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fpu1877m37331n45l%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Recent evidence supports the notion that transformation of undifferentiated neural stem cell (NSC) precursors may contribute
 to the development of glioblastoma multiforme (GBM). The over-expression and mutation of the epidermal growth factor receptor
 (EGFR), along with other cellular pathway mutations, plays a significant role in GBM maintenance progression. Though EGFR
 signaling is important in determining neural cell fate and conferring astrocyte differentiation, there is a limited understanding
 of its role in NSC and tumor stem cell (TSC) biology. We hypothesized that EGFR expression and mutation in post-natal NSCs
 may contribute to cellular aggressiveness including enhanced cellular proliferation, survival and migration. Stable subclones
 of C17.2 murine NSCs w...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2928293</comments>
            <pubDate>Fri, 23 Oct 2009 18:43:31 +0100</pubDate>
            <guid isPermaLink="false">2928293</guid>        </item>
        <item>
            <title>Primary CNS lymphoma in the elderly: temozolomide therapy and MGMT status</title>
            <link>http://www.medworm.com/index.php?rid=2913593&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F01873364r8l55334%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;This retrospective series explores temozolomide monotherapy in elderly patients with primary CNS lymphoma (PCNSL) and severe
 comorbidities. In 17 patients (62–90&amp;nbsp;years old), the complete response rate was 47%, median progression-free survival was
 5&amp;nbsp;months, and median overall survival was 21&amp;nbsp;months. Five of 17 patients (29.4%) had prolonged responses for at least 12&amp;nbsp;months
 and survived for more than 24&amp;nbsp;months. Three of these patients had a methylated O6-methylguanine-DNA methyltransferase (MGMT) promoter, while the MGMT status was not assessable in the remaining two patients.
 Temozolomide monotherapy appears to be effective in a subgroup of elderly PCNSL patients and deserves further evaluation.
 
	Content Type Journal ArticleCategory Clini...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2913593</comments>
            <pubDate>Tue, 20 Oct 2009 16:25:28 +0100</pubDate>
            <guid isPermaLink="false">2913593</guid>        </item>
        <item>
            <title>Prognostic value of O6-methylguanine-DNA methyltransferase status in glioblastoma patients, assessed by five different methods</title>
            <link>http://www.medworm.com/index.php?rid=2913594&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fy0663413l28j6325%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;This multicenter study assesses the value of O6-methylguanine-DNA methyltransferase (MGMT) status for predicting overall survival in glioblastoma patients. Five methods
 are used, to identify the approach with the best prognostic value. Eighty-one tumors were obtained from patients with glioblastomas
 treated by surgery and radiotherapy with concomitant temozolomide (TMZ) followed by adjuvant TMZ. MGMT promoter methylation was assessed by qualitative methyl-specific polymerase chain reaction (MSP), semiquantitative methyl-specific
 polymerase chain reaction (SQ-MSP), and pyrosequencing, while MGMT expression was measured at the RNA level by quantitative
 real-time PCR (Q-RT-PCR) and at the protein level by immunohistochemistry (IHC). MGMT promoter methylation as evaluat...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2913594</comments>
            <pubDate>Tue, 20 Oct 2009 16:25:27 +0100</pubDate>
            <guid isPermaLink="false">2913594</guid>        </item>
        <item>
            <title>The role of salvage reirradiation for malignant gliomas that progress on bevacizumab</title>
            <link>http://www.medworm.com/index.php?rid=2905888&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fx0r5667624253j38%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Bevacizumab and irinotecan are effective against recurrent malignant gliomas. However, at subsequent progression, patients
 rarely respond to a second bevacizumab-containing chemotherapeutic regimen. Salvage re-irradiation with bevacizumab for recurrent
 but bevacizumab naive malignant gliomas showed encouraging results. We performed a retrospective review of the medical records
 of 23 patients treated with either fractionated stereotactic radiotherapy (FSRT) or stereotactic radiosurgery (SRS) after
 progression on an initial bevacizumab regimen. Patients were treated after re-irradiation with bevacizumab but combined with
 a different chemotherapy. We then compared them to another 23 patients who progressed on an initial bevacizumab&amp;nbsp;+&amp;nbsp;chemotherapy
 regimen. T...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2905888</comments>
            <pubDate>Fri, 16 Oct 2009 17:57:42 +0100</pubDate>
            <guid isPermaLink="false">2905888</guid>        </item>
        <item>
            <title>Can permeability measurements add to blood volume measurements in differentiating tumefactive demyelinating lesions from high grade gliomas using perfusion CT?</title>
            <link>http://www.medworm.com/index.php?rid=2905889&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fj0p044206405w417%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Tumefactive demyelinating lesions (TDLs) can mimic a neoplasm on conventional imaging and may necessitate biopsy for diagnosis.
 The purpose of this study was to differentiate TDLs from high grade gliomas based on physiologic (permeability) and hemodynamic
 (blood volume) parameters using perfusion CT. Five patients who presented with tumefactive enhancing lesions on initial MRI
 that mimicked a neoplasm underwent perfusion CT. We compared the perfusion CT parameters of these patients with those of 24
 patients with high grade gliomas. TDLs showed lower permeability surface area product (PS) (0.8&amp;nbsp;±&amp;nbsp;0.2 vs 2.4&amp;nbsp;±&amp;nbsp;1.4&amp;nbsp;ml/100&amp;nbsp;g/min,
 P-value 0.014) and lower cerebral blood volume (CBV) (1.0&amp;nbsp;±&amp;nbsp;0.2 vs 2.8&amp;nbsp;±&amp;nbsp;1.2&amp;nbsp;ml/100...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2905889</comments>
            <pubDate>Thu, 15 Oct 2009 06:13:11 +0100</pubDate>
            <guid isPermaLink="false">2905889</guid>        </item>
        <item>
            <title>Methotrexate-induced myelopathy responsive to substitution of multiple folate metabolites</title>
            <link>http://www.medworm.com/index.php?rid=2887782&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fj5155j7267w82306%2F</link>
            <description>We report
 the case of a woman with breast cancer and meningeal carcinomatosis who developed severe progressive myelopathy after four
 cycles of intrathecal MTX administration. We substituted high doses of the key metabolites of the methyl-transfer pathway:
 S-adenosylmethionine (SAM), 200&amp;nbsp;mg three times daily i.v.; folinate, 20&amp;nbsp;mg four times daily i.v.; cyanocobalamin, 100&amp;nbsp;μg once
 daily i.v.; and methionine, 5&amp;nbsp;g daily p.o. The patient’s paraparesis improved rapidly thereafter, and magnetic resonance (MR)
 imaging showed resolution of the intramedullary lesions. Genetic analyses revealed homozygosity for the A allele of methylenetetrahydrofolate
 reductase (MTHFR) c.1298A&amp;gt;C (p.E429A), whereas other genetic variants of folate/methionine metabolism associated with ...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2887782</comments>
            <pubDate>Sun, 11 Oct 2009 07:26:01 +0100</pubDate>
            <guid isPermaLink="false">2887782</guid>        </item>
        <item>
            <title>Challenges in management of patients with intracranial germ cell tumor and diabetes insipidus treated with cisplatin and/or ifosfamide based chemotherapy</title>
            <link>http://www.medworm.com/index.php?rid=2883844&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fh864806g84h223w7%2F</link>
            <description>In conclusion, DI is a risk factor for
 complications when cisplatin and/or ifosfamide based protocols are used. The role of these agents in the management of ICGT
 should be carefully evaluated and guidelines for management of DI established.
 
	Content Type Journal ArticleCategory Clinical Study - Patient StudyDOI 10.1007/s11060-009-0033-zAuthors
		Samina Afzal, Hospital for Sick Children Division of Haematology/Oncology/Neuro-Oncology 555 University Avenue Toronto M5G 1X8 CanadaDiane Wherrett, Hospital for Sick Children Division of Endocrinology Toronto CanadaUte Bartels, Hospital for Sick Children Division of Haematology/Oncology/Neuro-Oncology 555 University Avenue Toronto M5G 1X8 CanadaUri Tabori, Hospital for Sick Children Division of Haematology/Oncology/Neuro-Oncology 555 Universi...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2883844</comments>
            <pubDate>Sat, 10 Oct 2009 07:28:57 +0100</pubDate>
            <guid isPermaLink="false">2883844</guid>        </item>
        <item>
            <title>Disease stabilization of progressive olfactory neuroblastoma (esthesioneuroblastoma) under treatment with sunitinib mesylate</title>
            <link>http://www.medworm.com/index.php?rid=2883846&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F83676w7xu28u6705%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Olfactory neuroblastoma (esthesioneuroblastoma) is a rare neoplasm of the olfactory epithelium in the upper nasal cavity.
 Here, we report the case of a 69-year-old man who presented with massive progression of a metastatic esthesioneuroblastoma
 after endonasal resection, functional neck dissection, and radiotherapy of local and distant tumor relapses. After exhaustion
 of all conventional therapeutic options, we initiated treatment with the oral multityrosinekinase inhibitor sunitinib mesylate.
 Using this drug, significant improvement of clinical symptoms, disease stabilization, and recovery from Karnofsky index of
 40% to 70% could be achieved in the absence of significant adverse drug effects. The patient died 15&amp;nbsp;months after initiation
 of sunitinib therapy d...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2883846</comments>
            <pubDate>Sat, 10 Oct 2009 07:28:56 +0100</pubDate>
            <guid isPermaLink="false">2883846</guid>        </item>
        <item>
            <title>Trigeminal nerve root entry zone pilocytic astrocytoma in an adult: a rare case of an extraparenchymal tumor</title>
            <link>http://www.medworm.com/index.php?rid=2883845&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fg0176m6v46090k43%2F</link>
            <description>We describe a pilocytic astrocytoma of the CPA that was found to arise from the
 proximal portion of trigeminal nerve without any anatomic continuity with the brain stem and the cerebellum. Pre-operative
 MRI suggested a schwannoma. The proposed origin of this extremely rare tumor is the root entry zone of the involved nerve.
 The tumor was completely resected via a suboccipital retrosigmoid approach.
 
	Content Type Journal ArticleCategory Case ReportDOI 10.1007/s11060-009-0020-4Authors
		Formica Francesco, Università Politecnica delle Marche Clinica di Neurochirurgia v. Conca no 71 60020 Ancona ItalyIacoangeli Maurizio, Università Politecnica delle Marche Clinica di Neurochirurgia v. Conca no 71 60020 Ancona ItalyChiriatti Stefano, Università Politecnica delle Marche Clinica di Neuroc...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2883845</comments>
            <pubDate>Sat, 10 Oct 2009 07:28:56 +0100</pubDate>
            <guid isPermaLink="false">2883845</guid>        </item>
        <item>
            <title>Utility of functional diffusion maps to monitor a patient diagnosed with gliomatosis cerebri</title>
            <link>http://www.medworm.com/index.php?rid=2877443&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fl6u11v561n225074%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Diffusion-weighted magnetic resonance imaging (DWI) is a sensitive imaging biomarker for tumor cellularity. Functional diffusion
 maps (fDMs), which examine voxel-by-voxel changes in the apparent diffusion coefficient (ADC) calculated from serial DWIs,
 have previously been applied to regions of contrast-enhancement; however, application of fDMs to non-enhancing brain tumors
 has not been pursued. In this case study we demonstrate the utility of applying fDMs to regions of abnormal FLAIR signal intensity
 in a patient diagnosed with gliomatosis cerebri: a relatively rare, infiltrative, non-enhancing brain tumor. The absolute
 volume of hypercellularity extracted from fDMs was useful in tracking tumor growth, which correlated in time with a progressive
 decline in neurol...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2877443</comments>
            <pubDate>Thu, 08 Oct 2009 07:04:49 +0100</pubDate>
            <guid isPermaLink="false">2877443</guid>        </item>
        <item>
            <title>Distribution, cellular localization, and therapeutic potential of the tumor-associated antigen Ku70/80 in glioblastoma multiforme</title>
            <link>http://www.medworm.com/index.php?rid=2873310&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fu118261471jx13u2%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Antibodies specifically targeting tumor-associated antigens have proved to be important tools in the treatment of human cancer.
 A desirable target antigen should be unique to tumor cells, abundantly expressed, and readily available for antibody binding.
 The Ku70/80 DNA-repair protein is expressed in the nucleus of most cells; it is, however, also present on the cell surface
 of tumor cell lines, and antibodies binding Ku70/80 at the cell surface were recently shown to internalize into tumor cells.
 To evaluate the potential of Ku70/80-antigen as a therapeutic target for immunotoxins in glioblastoma multiforme, we investigated
 binding and localization of Ku70/80-specific antibodies in tissue samples from glioblastomas and normal human brains, and
 in glioma cell cultu...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2873310</comments>
            <pubDate>Wed, 07 Oct 2009 06:59:00 +0100</pubDate>
            <guid isPermaLink="false">2873310</guid>        </item>
        <item>
            <title>Clinical and epidemiological characteristics of pediatric gliosarcomas</title>
            <link>http://www.medworm.com/index.php?rid=2870077&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fr41k251n67755545%2F</link>
            <description>In conclusion, GS is a very rare tumor entity in children. Literature review suggests a relatively higher incidence
 in infants and in patients with a previous history of radiotherapy.
 
	Content Type Journal ArticleCategory Clinical Study - Patient StudyDOI 10.1007/s11060-009-0021-3Authors
		Michael Karremann, Martin Luther University Halle-Wittenberg Department of Pediatrics and Adolescence Medicine Halle GermanyUlrike Rausche, Martin Luther University Halle-Wittenberg Department of Pediatrics and Adolescence Medicine Halle GermanyGudrun Fleischhack, University Hospital Bonn Department of Pediatrics Bonn GermanyMichaela Nathrath, Technische Universität München Department of Pediatrics Munich GermanyTorsten Pietsch, University of Bonn Institute of Neuropathology Bonn GermanyChristof M. ...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2870077</comments>
            <pubDate>Tue, 06 Oct 2009 12:42:26 +0100</pubDate>
            <guid isPermaLink="false">2870077</guid>        </item>
        <item>
            <title>Identification of the role of Smad interacting protein 1 (SIP1) in glioma</title>
            <link>http://www.medworm.com/index.php?rid=2870076&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F2746042453624274%2F</link>
            <description>This study supports the rationale for developing SIP1
 as a potential therapeutic and diagnostic target for gliomas.
 
	Content Type Journal ArticleCategory Laboratory Investigation - Human/Animal TissueDOI 10.1007/s11060-009-0015-1Authors
		Microgene Xia, The University of Hong Kong Integrative Laboratory Pokfulam, Hong Kong ChinaMinghua Hu, Yijishan Hospital, Wannan Medical College Wuhu 241001 ChinaJun Wang, Yijishan Hospital, Wannan Medical College Wuhu 241001 ChinaYajun Xu, Yijishan Hospital, Wannan Medical College Wuhu 241001 ChinaXiaobing Chen, Henan Tumor Hospital Department of Internal Medicine Zhengzhou 450008 ChinaYuedong Ma, The First Affiliated Hospital of Sun Yat-sen University Department of Internal Medicine Guangzhou 510080 ChinaLei Su, The First Affiliated Hospital of Sun Y...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2870076</comments>
            <pubDate>Tue, 06 Oct 2009 12:42:26 +0100</pubDate>
            <guid isPermaLink="false">2870076</guid>        </item>
        <item>
            <title>The cell growth inhibitory transcription factor C/EBPδ is expressed in human meningiomas in association with low histological grade and proliferation index</title>
            <link>http://www.medworm.com/index.php?rid=2870078&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fhu572002mr770725%2F</link>
            <description>In this study,
 C/EBPδ immunohistochemical expression was assessed in 49 meningiomas of different histotype and grade and correlated with
 a variety of clinico-pathological data and with the overall and recurrence-free survival of the patients. Positive staining
 was observed in the nuclei of neoplastic cells in 22 out of the 49 cases analyzed. C/EBPδ expression was significantly associated
 with a low histological grade and proliferation index, reflected by low Ki-67 labeling index (LI) and mitotic activity, and
 with the presence of intra-tumoral inflammatory infiltrate and the absence of necrosis. In addition, the absence of C/EBPδ
 was significantly correlated with a shorter disease-free interval. Our findings suggest that C/EBPδ expression may prevent
 the development of recurrenc...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2870078</comments>
            <pubDate>Tue, 06 Oct 2009 12:42:25 +0100</pubDate>
            <guid isPermaLink="false">2870078</guid>        </item>
        <item>
            <title>Pituitary metastasis of Merkel cell carcinoma</title>
            <link>http://www.medworm.com/index.php?rid=2870079&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F133u2213n8602064%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Merkel cell carcinoma (MCC) is a malignant neuroendocrine tumor of the skin that demonstrates a remarkable tendency to metastasize.
 However, only a few cases of MCC brain metastases have been reported in the literature. We here present a unique case of a
 pituitary metastasis of MCC in a 65-year-old patient with a history of pituitary adenoma. This case is particularly novel
 due to the fact that the primary site of the MCC is unknown.
 
	Content Type Journal ArticleCategory Case ReportDOI 10.1007/s11060-009-0025-zAuthors
		Alberto Feletti, University of Padova Department of Neurosurgery, Treviso Hospital Piazzale Ospedale, 1 31100 Treviso ItalyElisabetta Marton, University of Padova Department of Neurosurgery, Treviso Hospital Piazzale Ospedale, 1 31100 Treviso ItalyS...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2870079</comments>
            <pubDate>Tue, 06 Oct 2009 12:42:24 +0100</pubDate>
            <guid isPermaLink="false">2870079</guid>        </item>
        <item>
            <title>Feasibility, safety, and outcome of frameless image-guided robotic radiosurgery for brain metastases</title>
            <link>http://www.medworm.com/index.php?rid=2863537&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ff8q6268350210r75%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;We prospectively analyzed the safety and outcome of frameless image-guided robotic stereotactic radiosurgery (SRS) for treatment
 of brain metastases in patients that would have otherwise been treated with frame-based techniques. During a three-year period,
 333 patients with 783 brain metastases of various histologies underwent 391 outpatient SRS procedures. Fifty-five percent
 of patients had multiple brain metastases. The median (mean) tumor volume was 1.0&amp;nbsp;cc (2.7&amp;nbsp;cc). The mean prescribed tumor dose
 was 18.5&amp;nbsp;Gy (±1.3&amp;nbsp;Gy). Local/distant tumor recurrences were treated by additional SRS for patients with stable systemic disease.
 Survival and freedom from local tumor recurrence was analyzed with the Kaplan–Meier method. Prognostic factors were ob...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2863537</comments>
            <pubDate>Sun, 04 Oct 2009 05:43:25 +0100</pubDate>
            <guid isPermaLink="false">2863537</guid>        </item>
        <item>
            <title>Immunotherapy of pediatric brain tumor patients should include an immunoprevention strategy: a medical hypothesis paper</title>
            <link>http://www.medworm.com/index.php?rid=2863538&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F7156161262821n7k%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Adults diagnosed with Glioblastoma multiforme (GBM) are frequently faced with a 7% chance of surviving 2&amp;nbsp;years compared with
 pediatric patients with GBM who have a 26% survival rate. Our recent screen of possible glioma-associated antigen precursor
 protein (TAPP) profiles displayed from different types of pediatric brain tumors showed that pediatric patients contained
 a subset of the tumor antigens displayed by adult GBM patients. Adult GBM possess at least 27 tumor antigens that can potentially
 stimulate T cell immune responses, suggesting that these tumors are quite antigenic. In contrast, pediatric brain tumors only
 expressed nine tumor antigens with mRNA levels that were equivalent to those displayed by adult GBM. These tumor-associated
 antigens could be ...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2863538</comments>
            <pubDate>Sun, 04 Oct 2009 05:43:24 +0100</pubDate>
            <guid isPermaLink="false">2863538</guid>        </item>
        <item>
            <title>Central nervous system involvement in CD4+/CD56+ hematodermic neoplasm: a report of two cases</title>
            <link>http://www.medworm.com/index.php?rid=2863539&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F83jq514674434267%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;CD4+/CD56+ hematodermic neoplasm, formerly known as blastic NK-cell lymphoma, is an uncommon, aggressive non-Hodgkin’s lymphoma
 with cutaneous, lymph node, and bone marrow involvement at presentation. The disease is characterized by early leukemic phase;
 however, central nervous system involvement is rarely reported. Herein we describe two cases of CD4+/CD56+ hematodermic neoplasm
 with meningeal manifestation. Microscopic analysis and flow cytometry of cerebrospinal fluid proved to be diagnostic; however,
 imaging studies were not informative. These observations call attention to the possibility of central nervous system involvement,
 which could be more common than expected previously. Authors recommend routine cerebrospinal fluid analysis and prophylactic
 intrat...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2863539</comments>
            <pubDate>Fri, 02 Oct 2009 05:49:17 +0100</pubDate>
            <guid isPermaLink="false">2863539</guid>        </item>
        <item>
            <title>Anti-CV2 associated cerebellar degeneration after complete response to chemoradiation of head and neck carcinoma</title>
            <link>http://www.medworm.com/index.php?rid=2863540&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fdp7063344304012t%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Paraneoplastic cerebellar degeneration is a rare neurological disorder that frequently precedes the detection of malignancy.
 Here, we report the case of a 60&amp;nbsp;year-old woman with locally advanced squamous cell carcinoma of the tongue who developed
 a subacute cerebellar syndrome associated with the presence of anti-CV2/CRMP5 antibodies in the cerebrospinal fluid, after
 achieving complete remission of the primary tumor and the involved cervical lymph nodes by chemoradiation. The patient’s symptoms
 on presentation were dizziness and gait unsteadiness. On examination she showed dysarthria, nystagmus and limb and gait ataxia.
 The diagnosis of paraneoplastic cerebellar syndrome was made on the basis of the clinical findings and immunological testing
 that revealed ...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2863540</comments>
            <pubDate>Thu, 01 Oct 2009 18:16:30 +0100</pubDate>
            <guid isPermaLink="false">2863540</guid>        </item>
        <item>
            <title>CT and MRI findings with histopathologic correlation of a unique bilateral orbital mantle cell lymphoma in Graves’ disease: a case report and brief review of literature</title>
            <link>http://www.medworm.com/index.php?rid=2856505&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fkp7527l774658040%2F</link>
            <description>We present an unusual case report of a patient with Graves’ disease and no
 previous history of lymphoma, who was found to have bilateral orbital mantle cell lymphoma on CT and MR imaging which was
 confirmed histopathologically. To our knowledge, there have been no previously described cases of bilateral mantle cell lymphoma
 in Graves’ disease. Of particular radiologic interest, the left orbital mass presented in a bicompartmental fashion with a
 discreet intraconal component separated by a fat plane from an extraconal component that extended intraconally. In our review
 of radiologic literature, this presentation has not been described previously.
 
	Content Type Journal ArticleCategory Case ReportDOI 10.1007/s11060-009-0019-xAuthors
		Asif Abdullah, University of Toledo Medical Cen...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2856505</comments>
            <pubDate>Wed, 30 Sep 2009 18:27:59 +0100</pubDate>
            <guid isPermaLink="false">2856505</guid>        </item>
        <item>
            <title>Amplification and overexpression of KIT, PDGFRA, and VEGFR2 in medulloblastomas and primitive neuroectodermal tumors</title>
            <link>http://www.medworm.com/index.php?rid=2839830&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fq771vw6541k34541%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Medulloblastomas (MB) and primitive neuroectodermal tumors (PNET) are the most common malignant brain tumors in children.
 These two tumor types are histologically similar, but have different genetic backgrounds and clinical outcomes. Other brain
 tumors, such as gliomas, frequently have coamplification and overexpression of receptor tyrosine kinases KIT, platelet-derived
 growth factor receptor alpha (PDGFRA), and vascular endothelial growth factor receptor 2 (VEGFR2). We investigated protein
 expression and gene copy numbers of KIT, PDGFRA, and VEGFR2 in 41 MB and 11 PNET samples by immunohistochemistry (IHC) and
 chromogenic in&amp;nbsp;situ hybridization (CISH). KIT and PDGFRA expression was detected in both MBs and PNETs, whereas VEGFR2 expression
 was weak in these tu...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2839830</comments>
            <pubDate>Fri, 25 Sep 2009 05:48:24 +0100</pubDate>
            <guid isPermaLink="false">2839830</guid>        </item>
        <item>
            <title>The oncogenic roles of Notch1 in astrocytic gliomas in vitro and in vivo</title>
            <link>http://www.medworm.com/index.php?rid=2833066&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ff76573260821mw07%2F</link>
            <description>In this study, Notch1 overexpression was observed
 in the majority of 45 astrocytic gliomas with different grades and in U251MG glioma cells. Transfection of siRNA targeting
 Notch1 into U251 cells in vitro downregulated Notch1 expression, associated with inhibition of cell growth, arrest of cell
 cycle, reduction of cell invasiveness, and induction of cell apoptosis. Meanwhile, tumor growth was delayed in established
 subcutaneous gliomas in nude mice treated with Notch1 siRNA in vivo. These results suggest that Notch1 plays an important
 oncogenic role in the development and progression of astrocytic gliomas. Furthermore, knockdown of Notch1 expression by siRNA
 simultaneously downregulated the expression of EGFR and the important components of its downstream pathways, including PI3K,
 p...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2833066</comments>
            <pubDate>Tue, 22 Sep 2009 15:41:51 +0100</pubDate>
            <guid isPermaLink="false">2833066</guid>        </item>
        <item>
            <title>In vivo evaluation of intracellular drug-nanocarriers infused into intracranial tumours by convection-enhanced delivery: distribution and radiosensitisation efficacy</title>
            <link>http://www.medworm.com/index.php?rid=2825699&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ffr67p4u653832600%2F</link>
            <description>The objective of the present study was to investigate the interest of convection-enhanced delivery (CED) for the administration
 of a nanocarrier-based radiosensitizing chemotherapy in the rat brain. Pursuing on newly developed lipid nanocapsules (LNC)
 that can be internalised within brain tumour cells, we studied their intracerebral distribution when labelled with fluorescent
 Nile red (NR). As paclitaxel (Px) represents an interesting radiosensitiser, we also evaluated the potential radiosensitising
 effects of Px-loaded LNC administered through CED in the 9L intracranial rat glioblastoma model. The distribution study demonstrated
 that CED injection of NR-loaded LNC (NR-LNC) improved significantly the volume of distribution of NR when matched with simple
 injection (by about 150 fold)....</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2825699</comments>
            <pubDate>Mon, 21 Sep 2009 05:31:40 +0100</pubDate>
            <guid isPermaLink="false">2825699</guid>        </item>
        <item>
            <title>A phase II prospective study of sequential myeloablative chemotherapy with hematopoietic stem cell rescue for the treatment of selected high risk and recurrent central nervous system tumors</title>
            <link>http://www.medworm.com/index.php?rid=2815705&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F36134143x4042v12%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;High risk/recurrent CNS tumors have a poor prognosis. We studied tandem high dose chemotherapy (HDC) with hematopoietic progenitor
 stem cell rescues (HPCR) as potentially curative therapy. Twenty-four patients (mean age 6.8&amp;nbsp;years) were enrolled, 19 underwent
 HDC/HPCR. Diagnoses were medulloblastoma (n&amp;nbsp;=&amp;nbsp;9), germ cell tumor (n&amp;nbsp;=&amp;nbsp;4), high grade astrocytoma (n&amp;nbsp;=&amp;nbsp;2), supratentorial PNET (n&amp;nbsp;=&amp;nbsp;1), pineoblastoma (n&amp;nbsp;=&amp;nbsp;2), or papillary meningioma (n&amp;nbsp;=&amp;nbsp;1). Cytoreduction regimen #1 consisted of carboplatin (500&amp;nbsp;mg/m2)&amp;nbsp;×&amp;nbsp;3&amp;nbsp;days, etoposide (250&amp;nbsp;mg/m2) × 3&amp;nbsp;days, and thiotepa (300&amp;nbsp;mg/m2) × 3&amp;nbsp;days. Patients without progression or excessive toxicity (n&amp;nbsp;=&amp;nbsp;11), received ...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2815705</comments>
            <pubDate>Sun, 20 Sep 2009 15:32:40 +0100</pubDate>
            <guid isPermaLink="false">2815705</guid>        </item>
        <item>
            <title>Bortezomib sensitizes primary human esthesioneuroblastoma cells to TRAIL-induced apoptosis</title>
            <link>http://www.medworm.com/index.php?rid=2815706&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F0u047l05m175810w%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;TNF-related apoptosis-inducing ligand (TRAIL), a promising novel anti-cancer cytokine of the TNF superfamily, and Bortezomib,
 the first-in-class clinically used proteasome inhibitor, alone or in combination have been shown to efficiently kill numerous
 tumor cell lines. However, data concerning primary human tumor cells are very rare. Using primary esthesioneuroblastoma cells
 we analyzed the anti-tumor potential and the mechanism employed by Bortezomib in combination with TRAIL for the treatment
 of this rare but aggressive tumor. Expression of components of the TRAIL pathway was analyzed in tumor specimens and isolated
 primary tumor cells at the protein level. Cells were treated with TRAIL, Bortezomib, and a combination thereof, and apoptosis
 induction was quantifi...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2815706</comments>
            <pubDate>Sun, 20 Sep 2009 05:38:04 +0100</pubDate>
            <guid isPermaLink="false">2815706</guid>        </item>
        <item>
            <title>Intratumoral concentrations of imatinib after oral administration in patients with glioblastoma multiforme</title>
            <link>http://www.medworm.com/index.php?rid=2815707&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fhj83107306h2m247%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Imatinib, an orally administered tyrosine kinase inhibitor of PDGF receptor, c-abl and c-kit, is currently in clinical trials
 to assess its efficacy in malignant gliomas. Although imatinib does not readily penetrate an intact blood–brain barrier (BBB),
 the extent to which it distributes into regions of high grade gliomas where the BBB is compromised has not been determined.
 Patients with recurrent high-grade gliomas for whom repeat surgical tumor debulking was clinically indicated received imatinib
 mesylate 600&amp;nbsp;mg orally once a day for seven days prior to surgery. Tissue samples were collected from different regions of
 the tumor and the approximate location of these samples was determined using frameless stereotactic neuronavigation. Plasma
 samples were obt...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2815707</comments>
            <pubDate>Sat, 19 Sep 2009 05:51:58 +0100</pubDate>
            <guid isPermaLink="false">2815707</guid>        </item>
        <item>
            <title>Neurocognitive training in patients with high-grade glioma: a pilot study</title>
            <link>http://www.medworm.com/index.php?rid=2810599&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fa361201371171480%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Although their neurocognitive performance is one of the major concerns of patients with high-grade gliomas (HGG) and although
 neurocognitive deficits have been described to be associated with negative outcome, neurocognitive rehabilitation is usually
 not integrated into the routine care of patients with malignant gliomas. In this pilot trial, a weekly group training session
 for attention, verbal, and memory skills was offered to patients with HGG with pre and post-training evaluation. Eleven patients,
 six with glioblastoma multiforme and five with WHO grade III gliomas, median age 50&amp;nbsp;years, with a Karnofsky performance score
 of 80–100 participated in ten group training sessions of 90&amp;nbsp;min. For evaluation at baseline and after the training by a neuropsych...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2810599</comments>
            <pubDate>Thu, 17 Sep 2009 23:33:24 +0100</pubDate>
            <guid isPermaLink="false">2810599</guid>        </item>
        <item>
            <title>Concomitant treatment of F98 glioma cells with new liposomal platinum compounds and ionizing radiation</title>
            <link>http://www.medworm.com/index.php?rid=2810600&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fnw4q57k503p24371%2F</link>
            <description>In conclusion, among the five platinum compounds tested,
 carboplatin and LipoplatinTM showed the best radiosensitizing effect. LipoplatinTM seems the most promising since it led to the best cellular incorporation and has already been reported to be less neurotoxic
 than other platinum compounds.
 
	Content Type Journal ArticleCategory Laboratory Investigation - Human/Animal TissueDOI 10.1007/s11060-009-0011-5Authors
		Gabriel Charest, Université de Sherbrooke Sherbrooke CanadaBenoit Paquette, Université de Sherbrooke Sherbrooke CanadaDavid Fortin, Université de Sherbrooke Sherbrooke CanadaDavid Mathieu, Université de Sherbrooke Sherbrooke CanadaLéon Sanche, Université de Sherbrooke Sherbrooke Canada
	

	
		Journal Journal of Neuro-OncologyOnline ISSN 1573-7373Print ISSN 0167-594X (S...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2810600</comments>
            <pubDate>Thu, 17 Sep 2009 12:19:55 +0100</pubDate>
            <guid isPermaLink="false">2810600</guid>        </item>
        <item>
            <title>Solitary intra-ventricular brain metastasis from a breast carcinoma</title>
            <link>http://www.medworm.com/index.php?rid=2767167&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F4773862265706661%2F</link>
            <description>We present the unusual case of a breast cancer patient who developed a
 solitary choroid plexus metastasis in the left lateral ventricle.
 
	Content Type Journal ArticleCategory Case ReportDOI 10.1007/s11060-009-9988-zAuthors
		Alessandro Della Puppa, Padua University Hospital Department of Neurosurgery Via Giustiniani 2, Azienda Ospedaliera di Padova 35128 Padua ItalySandro Dal Pos, Padua University Hospital Department of Neuro-Radiology Padua ItalyStefania Zovato, IOV IRCCS of Padua Department of Oncology Padua ItalyEnrico Orvieto, Padua University Hospital Department of Pathology Padua ItalyPietro Ciccarino, Padua University Hospital Department of Neurosurgery Via Giustiniani 2, Azienda Ospedaliera di Padova 35128 Padua ItalyRenzo Manara, Padua University Hospital Department of Neuro-Ra...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2767167</comments>
            <pubDate>Thu, 03 Sep 2009 06:14:33 +0100</pubDate>
            <guid isPermaLink="false">2767167</guid>        </item>
        <item>
            <title>New methods to assess trends in neuro-oncological care</title>
            <link>http://www.medworm.com/index.php?rid=2767166&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fc03g273823p6720r%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorDOI 10.1007/s11060-009-9999-9Authors
		Debraj Mukherjee, Neuro-Oncology Surgical Outcomes Research Laboratory Department of Neurosurgery and Oncology 1550 Orleans Street, Cancer Research Building II Room 253 Baltimore MD 21231 USADavid C. Chang, Neuro-Oncology Surgical Outcomes Research Laboratory Department of Surgery 1550 Orleans Street, Cancer Research Building II Room 253 Baltimore MD 21231 USAAlfredo Quiñones-Hinojosa, Neuro-Oncology Surgical Outcomes Research Laboratory Department of Neurosurgery and Oncology 1550 Orleans Street, Cancer Research Building II Room 253 Baltimore MD 21231 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=2767166</comments>
            <pubDate>Thu, 03 Sep 2009 06:14:33 +0100</pubDate>
            <guid isPermaLink="false">2767166</guid>        </item>
        <item>
            <title>Predictive value of multimodality MRI using conventional, perfusion, and spectroscopy MR in anaplastic transformation of low-grade oligodendrogliomas</title>
            <link>http://www.medworm.com/index.php?rid=2767168&amp;cid=s_33361_6_f&amp;fid=33361&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F41v91264m7315572%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The aim of our study was to evaluate the role of proton magnetic resonance (MR) spectroscopy and MR perfusion in the follow-up
 of low-grade gliomas, since conventional MR imaging (MRI) is not reliable in detecting the passage from a low- to high-grade
 tumor. Twenty-one patients with a World Health Organisation (WHO) grade&amp;nbsp;II glioma were followed up using proton MR spectroscopy,
 perfusion, and conventional MRIs. Follow-up MRIs had been performed at the third month of evolution and then twice a year,
 with an average of five MR studies per patient. Five out of the 21 patients had an anaplastic transformation. A choline to
 creatine ratio (choline/creatine ratio) above 2.4 is associated with an 83% risk of a malignant transformation in an average
 delay of 15.4&amp;nbs...</description>
            <author>Journal of Neuro-Oncology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2767168</comments>
            <pubDate>Thu, 03 Sep 2009 06:14:32 +0100</pubDate>
            <guid isPermaLink="false">2767168</guid>        </item>
    </channel>
</rss>
