Mehta Amikumar, Sonpavde Guru, Escudier Bernard
University of Alabama, Birmingham (UAB) Comprehensive Cancer Center, Birmingham, AL, USA.
Future Oncol. 2014 Aug;10(11):1819-26. doi: 10.2217/fon.14.120.
Multiple VEGF and mTOR inhibitors have provided improvements in median progression-free survival for metastatic renal cell carcinoma. Tivozanib is a potent and specific VEGFR-1, -2 and -3 tyrosine kinase inhibitor. Promising results led to the TIVO-I Phase III trial (n = 517) comparing tivozanib with sorafenib in patients who were either untreated or had received cytokines. This study met its primary end point by statistically significantly improving progression-free survival, but did impair overall survival, a secondary end point. Crossover from sorafenib to tivozanib may have confounded survival. Because of that detrimental survival, the US FDA rejected approval in May 2013, leading to interruption in its development for renal cell carcinoma.
多种血管内皮生长因子(VEGF)和雷帕霉素靶蛋白(mTOR)抑制剂已使转移性肾细胞癌的中位无进展生存期得到改善。替沃扎尼是一种强效且特异性的血管内皮生长因子受体(VEGFR)-1、-2和-3酪氨酸激酶抑制剂。有前景的结果促使开展了TIVO-1 III期试验(n = 517),该试验在未接受治疗或已接受细胞因子治疗的患者中比较替沃扎尼与索拉非尼。这项研究通过在统计学上显著改善无进展生存期达到了其主要终点,但确实损害了总生存期这一次要终点。从索拉非尼交叉至替沃扎尼可能混淆了生存期。由于生存期出现这种不利情况,美国食品药品监督管理局(FDA)于2013年5月拒绝批准,导致其用于肾细胞癌的研发中断。