Department of Urology, University of California, Davis, Medical Center, 4860 Y Street, Suite 3500, Sacramento, CA 95817, USA.
Urol Clin North Am. 2012 May;39(2):233-49, vii. doi: 10.1016/j.ucl.2012.02.002. Epub 2012 Mar 3.
Treatment of metastatic renal cell carcinoma (mRCC) has evolved dramatically within the past 10 years with the advent of therapy targeting the angiogenesis and mammalian target of rapamycin (mTOR) pathways. These therapies rapidly supplanted immunotherapy as a first-line systemic treatment option. Response rates, however, continue to vary, largely due to mRCC's clinical and molecular heterogeneity. This article reviews current understanding of mRCC biology and available treatments, discusses novel biomarkers that improve prognostication and may be able to predict response, and integrates available literature on surgical and systemic therapies into an individualized strategy.
过去 10 年来,针对血管生成和哺乳动物雷帕霉素靶蛋白(mTOR)途径的治疗方法的出现,转移性肾细胞癌(mRCC)的治疗发生了巨大变化。这些疗法迅速取代免疫疗法成为一线系统治疗选择。然而,反应率仍在继续变化,主要是由于 mRCC 的临床和分子异质性。本文综述了 mRCC 生物学和现有治疗方法的最新认识,讨论了改善预后并可能预测反应的新型生物标志物,并将关于手术和系统治疗的现有文献整合到个体化策略中。