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Combination of bevacizumab and lomustine with first recurrence of glioblastoma prolongs PFS but not OS

Al's Comment:

 We need to have a discussion about the value of increasing progression free survival (PFS) without increasing overall survival.  (The braintumor treatments group is the best place to discuss it). My thoughts are that  obviously, increasing PFS is good - you feel good for a longer period of time, but perhaps it may be better to try other things instead.  Shoot for increasing both PFS and overall survival.  There are a few interesting trials going on for recurrent GBM, and the Optune device has been shown to increase both PFS and OS.


Posted on: 11/23/2015

 

PUBLIC RELEASE: 

Combination of bevacizumab and lomustine with first recurrence of glioblastoma prolongs PFS but not OS

 

EUROPEAN ORGANISATION FOR RESEARCH AND TREATMENT OF CANCER

 

Results of EORTC trial 26101 presented today at The 20th Annual Scientific Meeting and Education Day of the Society for Neuro-Oncology showed that bevacizumab treatment in patients with progressive glioblastoma, despite prolonged progression-free survival, does not confer a survival advantage.

Prof. Dr. Wolfgang Wick of the Uniklinik Heidelberg and coordinator of this study says, "The future challenge is to identify those patients deriving benefit from that treatment."

With an annual incidence of approximately five cases per 100,000 persons, gliomas are the most frequently occurring brain tumor in adults. Glioblastomas represent roughly 60-70% of all gliomas, and for this type of glioma there is no curative treatment.

"Standard first line treatment consists of surgical resection followed by radiation and concomitant and adjuvant temozolomide therapy. For recurrence, there are treatment options, but we still have no standard treatment," points out Dr. Wick. "Phase II data from the BELOB trial had indicated that the combination of bevacizumab and lomustine might produce an overall survival benefit compared with either monotherapy for patients with first progression of a glioblastoma."

EORTC trial 26101 was coordinated by the EORTC Brain Tumor Group and included 437 patients at 44 sites located in eight countries: Austria, Belgium, France, Germany, Italy, Switzerland, The Netherlands, and the United Kingdom.

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This phase 3 trial was supported by an educational grant from F. Hoffmann-La Roche Ltd.

 


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