Evolving role of novel targeted agents in renal cell carcinoma
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作者:
Hutson, Thomas E.
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机构:
PA Baylor Sammons Canc Ctr, Genitourinary Oncol Program, Dallas, TX USA
US Oncol Res Network, Dallas, TX USACity Hope Comprehens Canc Ctr, Div Med Oncol, Duarte, CA 91010 USA
Hutson, Thomas E.
[3
,4
]
Figlin, Robert A.
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机构:
City Hope Comprehens Canc Ctr, Div Med Oncol, Duarte, CA 91010 USA
City Hope Natl Med Ctr, Div Med Oncol & Expt Therapeut, Duarte, CA USACity Hope Comprehens Canc Ctr, Div Med Oncol, Duarte, CA 91010 USA
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
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.
机构:
Univ Hosp, Hop St Andre, Dept Med Oncol & Radiotherapy, F-33075 Bordeaux, France
Univ Bordeaux 2, F-33076 Bordeaux, FranceUniv Hosp, Hop St Andre, Dept Med Oncol & Radiotherapy, F-33075 Bordeaux, France