Based on the US Food and Drug Administration's recent accelerated approval of Roche's Avastin (bevacizumab) in the treatment of HER2-negative metastatic breast cancer plus paclitaxel, oncologists will more than double their use of the drug as both a first- and second-line therapy, according to a survey conducted by USA-based GfK Market Measures.
The FDA's decision in February (Marketletter March 3) surprised industry observers as last year its Oncologic Drugs Advisory Committee voted five to four against approving the combination, arguing that the benefits did not outweigh the risks of toxicity (Marketletter December 10, 2007).
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