Renal cell carcinoma: molecular biology and targeted therapy

被引:48
作者
Su, Daniel [1 ]
Stamatakis, Lambros [1 ]
Singer, Eric A. [2 ,3 ]
Srinivasan, Ramaprasad [1 ]
机构
[1] NCI, Urol Oncol Branch, Ctr Canc Res, NIH, Bethesda, MD 20892 USA
[2] Rutgers Canc Inst New Jersey, Sect Urol Oncol, New Brunswick, NJ USA
[3] Univ Med & Dent New Jersey, Robert Wood Johnson Med Sch, New Brunswick, NJ USA
基金
美国国家卫生研究院;
关键词
immunotherapy; renal cell carcinoma; targeted therapy; HIGH-DOSE INTERLEUKIN-2; INTERFERON-ALPHA; PHASE-I; TRIAL; SUNITINIB; CANCER; EVEROLIMUS; ANTIBODY; SAFETY; TEMSIROLIMUS;
D O I
10.1097/CCO.0000000000000069
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose of reviewRenal cell carcinoma (RCC) continues to be the subject of vigorous clinical and translational investigation. Advances in systemic targeted therapies, new molecular pathways and immunotherapy approaches will be discussed.Recent findingsAgents targeting the vascular endothelial growth factor (VEGF) and/or the mammalian target of rapamycin (mTOR) pathways continue to be the mainstay for treating metastatic RCC (mRCC). Although enhanced target specificity has improved the toxicity profile associated with newer VEGF-pathway antagonists, durable complete responses remain the exception. Identification of novel pathways/agents, as well as the optimal sequencing and combination of existing targeted agents, remain areas of active study. In addition, emerging data from early clinical trials have reinvigorated interest in immunomodulatory agents.SummaryThe therapeutic armamentarium available to genitourinary oncologists continues to grow, but much work remains to be done to fully realize the potential of pathway-specific targeted strategies and immune-based approaches for mRCC.
引用
收藏
页码:321 / 327
页数:7
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