Department of Medical Oncology, Guy's Hospital, London, UK.
Hematol Oncol Clin North Am. 2011 Aug;25(4):853-69. doi: 10.1016/j.hoc.2011.05.003.
Insights into the biology of clear-cell renal cell carcinoma (CCRCC) have identified multiple pathways associated with the pathogenesis and progression of this cancer. This progress has led to the development of multiple agents targeting these pathways, including the tyrosine kinase inhibitors sorafenib, sunitinib, and pazopanib, the monoclonal antibody bevacizumab, and the mTOR inhibitors temsirolimus and everolimus. With the exception of temsirolimus, phase 3 trials tested these agents in patients with clear-cell histology; therefore, their efficacy in non-CCRCC is unclear. To date, there is no established effective therapy for patients with advanced non-CCRCC. This article focuses on treatment options for metastatic non-CCRCC.
对透明细胞肾细胞癌 (CCRCC) 生物学的深入了解已经确定了多个与该癌症的发病机制和进展相关的途径。这一进展导致了多种针对这些途径的药物的开发,包括酪氨酸激酶抑制剂索拉非尼、舒尼替尼和帕唑帕尼、单克隆抗体贝伐珠单抗以及 mTOR 抑制剂替西罗莫司和依维莫司。除了替西罗莫司,III 期临床试验在透明细胞组织学的患者中测试了这些药物;因此,它们在非 CCRCC 中的疗效尚不清楚。迄今为止,晚期非 CCRCC 患者尚无既定的有效治疗方法。本文重点介绍转移性非 CCRCC 的治疗选择。