نتایج جستجو برای: ependymoma

تعداد نتایج: 1663  

Journal: :The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques 2014
Gloria B Roldán Urgoiti Amitabh D Singh Roger Y Tsang Robert A Nordal Gerald Lim Jennifer A Chan Yves P Starreveld Paula A de Robles Bradly J Biagioni Mark G Hamilton Jacob C Easaw

BACKGROUND Ependymomas are rare tumors of the central nervous system whose management is controversial. This population-based study of adults and children with ependymoma aims to (1) identify clinical and treatment-related factors that impact survival and (2) determine if postoperative radiotherapy (RT) can improve survival of patients with subtotal resection (STR) to levels similar to patients...

Journal: :International journal of radiation oncology, biology, physics 2011
Maura Massimino Lorenza Gandola Salvina Barra Felice Giangaspero Cecilia Casali Paolo Potepan Concezio Di Rocco Paolo Nozza Paola Collini Elisabetta Viscardi Daniele Bertin Veronica Biassoni Armando Cama Claudia Milanaccio Piergiorgio Modena Rita Balter Giampiero Tamburrini Paola Peretta Maurizio Mascarin Giovanni Scarzello Paola Fidani Giuseppe Maria Milano Iacopo Sardi Lorenzo Genitori Maria Luisa Garrè

PURPOSE The protocols of the 1990s omitted or delayed irradiation, using upfront chemotherapy to spare the youngest children with ependymoma the sequelae of radiotherapy (RT). We treated 41 children under the age of 3 years with intracranial ependymoma between 1994 and 2003. PATIENTS AND METHODS After surgery, chemotherapy was given as follows: regimen I with four blocks of vincristine, high-...

2016
Theophilos Tzaridis Till Milde Kristian W. Pajtler Sebastian Bender David T. W. Jones Simone Müller Andrea Wittmann Magdalena Schlotter Andreas E. Kulozik Peter Lichter V. Peter Collins Olaf Witt Marcel Kool Andrey Korshunov Stefan M. Pfister Hendrik Witt

Ependymomas in children can arise throughout all compartments of the central nervous system (CNS). Highly malignant paediatric ependymoma subtypes are Group A tumours of the posterior fossa (PF-EPN-A) and RELA-fusion positive (ST-EPN-RELA) tumours in the supratentorial compartment. It was repeatedly reported in smaller series that accumulation of p53 is frequently observed in ependymomas and th...

2016

Sunitinib malate is a small multi-targeted tyrosine kinase inhibitor that inhibits vascular endothelial growth factor receptor (VEGFR), platelet-derived growth factor receptor (PDGFR) and stem cell factor receptor (KIT), which are highly expressed by some high-grade brain tumors. We conducted a phase II study to estimate the efficacy and further characterize the pharmacokinetics of sunitinib in...

Journal: :Neuro-oncology 2010
Terri S Armstrong Elizabeth Vera-Bolanos B Nebiyou Bekele Kenneth Aldape Mark R Gilbert

Ependymomas in adults are rare and often misdiagnosed. This study reports on a series of adult patients with confirmed ependymoma treated at The University of Texas M. D. Anderson Cancer Center (MDACC). Patients aged >17 and with ependymoma were identified, and clinical data were collected by retrospective chart review. Descriptive statistics were used to describe the clinical data, Kaplan-Meie...

Journal: :International journal of radiation oncology, biology, physics 2008
Stephanie E Combs Verena Kelter Thomas Welzel Wolfgang Behnisch Andreas E Kulozik Marc Bischof Holger Hof Jürgen Debus Daniela Schulz-Ertner

PURPOSE To assess the outcome of 57 patients with localized ependymomas treated with radiotherapy (RT). METHODS AND MATERIALS Fifty-seven patients with localized ependymomas were treated with RT. Histology was myxopapillary ependymoma (n = 4), ependymoma (n = 23), and anaplastic ependymoma (n = 30). In 16 patients, irradiation of the craniospinal axis (CSI) was performed with a median dose of...

C. Yavas, G. Yavas, H. Acar, O. Ata, P. Karabagli,

Multiple primary tumors in a single patient are relatively rare when four or more distinct lesions are considered. Herein, we report a case of woman with four different primary tumors: meningioma, renal angiomyolipoma, spinal ependymoma and high-grade soft tissue sarcoma. There was no family history and hereditary syndrome. The genetic analysis was completely normal. To best of our knowledge, t...

Journal: :AJNR. American journal of neuroradiology 1999
J Y Chung S K Lee K H Yang M K Song

We report a case of myxopapillary ependymoma presenting as a primary tumor of the subcutaneous tissue in the sacrococcygeal region. The mass was large, well-encapsulated, lobulated, and multiseptated, with varying signal intensity on T1- and T2-weighted MR images caused by hemorrhagic necrosis, blood degradation products, and calcification. Only a small viable portion enhanced after administrat...

Journal: :Neuro-oncology 2015
Jacques Grill

Standard of care for pediatric ependymoma comprises maximal surgery and focal radiotherapy. This is, however, not sufficient to cure all patients, and approximately one third will eventually relapse. With the exception of a study with a gamma-secretase inhibitor, most of the phase I/II trials performed to date in children with ependymoma have not been driven by a strong preclinical background, ...

2010
Matthieu Peyre Frédéric Commo Carmela Dantas-Barbosa Felipe Andreiuolo Stéphanie Puget Ludovic Lacroix Françoise Drusch Véronique Scott Pascale Varlet Audrey Mauguen Philippe Dessen Vladimir Lazar Gilles Vassal Jacques Grill

BACKGROUND Children with ependymoma may experience a relapse in up to 50% of cases depending on the extent of resection. Key biological events associated with recurrence are unknown. METHODOLOGY/PRINCIPAL FINDINGS To discover the biology behind the recurrence of ependymomas, we performed CGHarray and a dual-color gene expression microarray analysis of 17 tumors at diagnosis co-hybridized with...

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