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Clinical Trial Summary

This is a multi-institutional phase III clinical study of interventional type. The trial will include 220 patients with confirmed unifocal glioblastoma over a period of 3 years + 3 years of follow up. Patients with unifocal glioblastoma (diagnosis confirmed by histology on tumoral biopsy or surgical specimen) and who meet all eligibility criteria will be randomized in one chemoradiotherapy arm : - Conventional arm: 3-dimensional conformational radiotherapy + Temozolomide - Experimental arm : simultaneous-integrated boost with intensity-modulated radiotherapy guided by magnetic resonance spectroscopic imaging + Temozolomide The patient monitoring will be regular and standardized. The main objective of this study is to improve overall survival of patients treated in experimental group (with simultaneous integrated boost).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01507506
Study type Interventional
Source Institut Claudius Regaud
Contact
Status Terminated
Phase Phase 3
Start date March 15, 2011
Completion date January 2, 2020

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