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Onco Targets Ther. 2010 Oct 5;3:179-89.

The bevacizumab experience in advanced renal cell carcinoma.

Author information

1
Division of Oncology, Stanford University School of Medicine, Stanford, California, USA.

Abstract

Bevacizumab in combination with interferon alfa is now approved for treatment-naïve advanced renal cell carcinoma (RCC) in both the US and Europe. Its objective response rates of 30% and progression-free survival rates of 9-10 months are comparable to the other approved first-line multityrosine kinase inhibitors, sunitinib and pazopanib. Its advantages include a different toxicity profile and assurance of administration compliance given its intravenous formulation. Enthusiasm for its use is blunted by the increased costs, the potential infusion-related reactions, the associated interferon-related toxicities, and the inconvenience of its nonoral formulation. Further study is warranted to assess its efficacy both as a single agent and in combination with the targeted agents and other immunotherapies. With multiple agents now available for the treatment of advanced RCC, identification of patient and tumor-specific biomarkers to inform our choice of first-line therapy and the proper sequence of subsequent therapies is imperative.

KEYWORDS:

bevacizumab; interferon alfa; renal cell carcinoma

PMID:
21049084
PMCID:
PMC2962304

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