Evolving role of novel targeted agents in renal cell carcinoma

被引:0
|
作者
Hutson, Thomas E. [3 ,4 ]
Figlin, Robert A. [1 ,2 ]
机构
[1] City Hope Comprehens Canc Ctr, Div Med Oncol, Duarte, CA 91010 USA
[2] City Hope Natl Med Ctr, Div Med Oncol & Expt Therapeut, Duarte, CA USA
[3] PA Baylor Sammons Canc Ctr, Genitourinary Oncol Program, Dallas, TX USA
[4] US Oncol Res Network, Dallas, TX USA
来源
ONCOLOGY-NEW YORK | 2007年 / 21卷 / 10期
关键词
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The treatment of metastatic renal cell carcinoma (RCC) has changed dramatically over the past few years. An improved understanding of the biology of RCC has resulted in the development of novel targeted therapeutic agents that have altered the natural history of this disease. In particular, the hypoxia-inducible factor (HIF)/vascular endothelial growth factor (VEGF) path way and the mammalian target of rapamycin (mTOR) signal transduction pathway have been exploited. Sunitinib malate (Sutent), sorafenib tosylate (Nexavar), bevacizumab (Avastin)/interferon alfa, and temsirolimus (Torisel) have improved clinical outcomes in randomized trials by inhibiting these tumorigenic pathways. Combinations and sequences of these agents are being evaluated. Other novel multitargeted tyrosine kinase inhibitors (pazopanib and axitinib) and m TOR inhibitors (everolimus) are in clinical development. Recently reported and ongoing clinical trials will help further define the role of these agents as therapy for metastatic RCC.
引用
收藏
页码:1175 / 1180
页数:6
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