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FDA Grants Bevacizumab Full Approval for Glioblastoma

Jason M. Broderick @jasoncology
Published: Tuesday, Dec 05, 2017

Dr. Sandra Horning

Sandra Horning, MD
The FDA has granted bevacizumab (Avastin) a full approval for the treatment of adult patients with glioblastoma that progressed following prior therapy, according to Genentech, the manufacturer of the VEGF inhibitor.1

In safety data from the AVF3708g study, the most common all-grade adverse events in the single-agent bevacizumab arm were infection, fatigue, headache, hypertension, epistaxis, and diarrhea. Adverse events led to discontinuation in 4.8% of patients receiving bevacizumab. There were 2 patient deaths (retroperitoneal hemorrhage and neutropenic infection) that investigators considered as potentially related to bevacizumab treatment.
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TitleExpiration DateCME Credits
Community Practice Connections™: Overcoming Clinical Inertia in Glioblastoma Multiforme: The Experts Weigh-In on Recent Data Sets and Next Steps to Move the Field ForwardDec 21, 20191.5
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