Pan Qingqing, Wang Mengzhao
Department of Respiratory Medicine, Chinese Academy of Medical Sciences, Beijing 100730, China.
Zhongguo Fei Ai Za Zhi. 2011 Jul;14(7):606-12. doi: 10.3779/j.issn.1009-3419.2011.07.08.
Bevacizumab, the monoclonal antibody of vascular endothelial growth factor (VEGF) has been applied to the therapy of several neoplasms, but an appropriate biomarker to predict the efficacy has not been found. Those markers can originate from peripheral circulation, tumor tissue and genes. Some researches have found that low level of vascular cell adhesion molecule-1 (VCAM-1), E-selectin, angiopoietin 2 (Ang-2) in circulation or carbonic anhydrase 9 (CA9), CD31-microvessel density (CD31-MVD) in tumor tissue can predict better activity of bevacizumab. Moreover, high level of soluble VEGFR2 (sVEGFR2) in circulation or the ratio of phosphorylated-VEGFR2 (p-VEGFR2) and VEGFR2 in tumor tissue increasing has the same predictive function. As to the gene, VEGF-634 CC, VEGF-1498 TT and VEGFR2 H472Q are only related to the side effct. Thus more clinical tirals and basic researches should be performed to find out effective biomarkers in bevacizumab's therapy.
贝伐单抗,一种血管内皮生长因子(VEGF)单克隆抗体,已应用于多种肿瘤的治疗,但尚未找到合适的生物标志物来预测其疗效。这些标志物可来源于外周循环、肿瘤组织和基因。一些研究发现,循环中血管细胞黏附分子-1(VCAM-1)、E-选择素、血管生成素2(Ang-2)水平较低,或肿瘤组织中碳酸酐酶9(CA9)、CD31-微血管密度(CD31-MVD)较低,可预测贝伐单抗的疗效更佳。此外,循环中可溶性VEGFR2(sVEGFR2)水平较高,或肿瘤组织中磷酸化-VEGFR2(p-VEGFR2)与VEGFR2的比值升高,具有相同的预测功能。至于基因,VEGF-634 CC、VEGF-1498 TT和VEGFR2 H472Q仅与副作用有关。因此,应开展更多的临床试验和基础研究,以找出贝伐单抗治疗中的有效生物标志物。