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Abstract:
"Bevacizumab
is the first antiangiogenic therapy proven to slow metastatic disease
progression in patients with cancer. Although it has changed clinical
practice, some patients do not respond or gradually develop resistance,
resulting in rather modest gains in terms of overall survival. A major
challenge is to develop robust biomarkers that can guide selection of
patients for whom bevacizumab therapy is most beneficial. Here, we
discuss recent progress in finding such markers, including the first
results from randomized phase III clinical trials evaluating the
efficacy of bevacizumab in combination with comprehensive biomarker
analyses. In particular, these studies suggest that circulating levels
of short vascular endothelial growth factor A (VEGF-A) isoforms,
expression of neuropilin-1 and VEGF receptor 1 in tumors or plasma, and
genetic variants in VEGFA or its receptors are strong biomarker
candidates. The current challenge is to expand this first set of markers
and to validate it and implement it into clinical practice. A first
prospective biomarker study known as MERiDiAN, which will treat patients
stratified for circulating levels of short VEGF-A isoforms with
bevacizumab and paclitaxel, is planned and will hopefully provide us
with new directions on how to treat patients more efficiently."
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