贝伐单抗
医学
生物标志物
肿瘤科
抗血管生成治疗
血管内皮生长因子
内科学
血管内皮生长因子受体
血管内皮生长因子A
临床试验
神经肽1
生物信息学
化疗
生物化学
化学
生物
作者
Diether Lambrechts,Heinz‐Josef Lenz,Sanne de Haas,Peter Carmeliet,Stefan Scherer
标识
DOI:10.1200/jco.2012.46.2762
摘要
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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