Larkin James M G, Chowdhury Simon, Gore Martin E
Royal Marsden Hospital, London, UK.
Nat Clin Pract Oncol. 2007 Aug;4(8):470-9. doi: 10.1038/ncponc0901.
In metastatic renal cell carcinoma (RCC) immunotherapy results in a small but important improvement in overall survival, but a need exists to develop more-effective systemic therapies. Recent developments in our understanding of the molecular biology of RCC have identified several pathways associated with the development of the disease. A number of strategies designed specifically to target these pathways have resulted. Initial studies have shown marked clinical benefits of so-called 'targeted therapies'. Sunitinib, sorafenib and axitinib are kinase inhibitors that inhibit the VEGF, platelet-derived growth factor and c-kit receptor tyrosine kinases. Bevacizumab is a monoclonal antibody that is directed against VEGF. Temsirolimus inhibits the mammalian target of rapamycin. These agents have all shown considerable activity with manageable toxicity in phase II and III studies in both previously treated and untreated patients. In phase III studies, sorafenib and bevacizumab have been associated with prolonged progression-free survival compared with placebo. Phase III data have shown improvements in progression-free and overall survival with sunitinib and temsirolimus, respectively, compared with interferon alfa. Additional studies are needed to determine the optimum utilization of these agents at the appropriate stage of disease and in the best combinations for maximal clinical benefit.
在转移性肾细胞癌(RCC)中,免疫疗法可使总生存期得到虽小但重要的改善,但仍需要开发更有效的全身治疗方法。近年来,我们对RCC分子生物学的认识取得了进展,确定了几种与该疾病发展相关的途径。因此产生了一些专门针对这些途径设计的策略。初步研究显示了所谓“靶向疗法”显著的临床益处。舒尼替尼、索拉非尼和阿昔替尼是抑制血管内皮生长因子(VEGF)、血小板衍生生长因子和c-kit受体酪氨酸激酶的激酶抑制剂。贝伐单抗是一种针对VEGF的单克隆抗体。替西罗莫司可抑制哺乳动物雷帕霉素靶蛋白。在II期和III期研究中,这些药物在既往接受治疗和未接受治疗的患者中均显示出相当的活性且毒性可控。在III期研究中,与安慰剂相比,索拉非尼和贝伐单抗与无进展生存期延长相关。III期数据显示,与干扰素α相比,舒尼替尼和替西罗莫司分别使无进展生存期和总生存期得到改善。需要进一步研究以确定在疾病的适当阶段对这些药物的最佳应用方式以及能带来最大临床获益的最佳联合用药方案。