Consultant and Associate Lecturer in Medical Oncology, Oncology Centre (Box 193), Addenbrooke's Hospital, Hills Road, Cambridge CB2 0QQ, UK.
Ther Adv Med Oncol. 2010 Nov;2(6):367-80. doi: 10.1177/1758834010380101.
Angiogenesis has been identified as a relevant target for melanoma experimental therapeutics, based on preclinical and clinical studies. A variety of angiogenesis inhibitors are currently being tested in both metastatic and adjuvant melanoma clinical trials. To date, the most promising evidence of benefit is based on a statistically nonsignificant trend in survival gain reported in a randomized phase II trial combining bevacizumab, a monoclonal antibody targeting vascular endothelial growth factor, with cytotoxic chemotherapy. Larger phase III studies are required to determine the true extent of clinical benefit with this class of agents. Key to these clinical trials is the need to include translational endpoints, since correlation of biological and clinical data will provide the opportunity to identify biomarkers predictive of treatment response. These biological studies will also aid our, as yet, poor understanding of the mechanism of action of angiogenesis inhibitors, as well as drug-related side effects. Finally, if these trials show meaningful clinical benefit, then careful consideration will need to be given when designing second-generation trials, in the light of novel gene-directed therapies currently showing promise in melanoma.
血管生成已被确定为黑色素瘤实验治疗的一个相关靶点,这基于临床前和临床研究。目前,各种血管生成抑制剂正在转移性和辅助性黑色素瘤临床试验中进行测试。迄今为止,最有希望的获益证据基于一项联合贝伐单抗(一种针对血管内皮生长因子的单克隆抗体)与细胞毒性化疗的随机 II 期试验报告的生存获益的统计学无显著趋势。需要更大规模的 III 期研究来确定此类药物的实际临床获益程度。这些临床试验的关键是需要纳入转化终点,因为生物和临床数据的相关性将提供机会来确定预测治疗反应的生物标志物。这些生物学研究也将有助于我们目前对血管生成抑制剂作用机制以及与药物相关的副作用的理解。最后,如果这些试验显示出有意义的临床获益,那么在设计第二代试验时需要仔细考虑,因为目前在黑色素瘤中显示出前景的新型基因靶向治疗。