New agents in renal cell carcinoma

被引:24
作者
Dabney, Raetasha [1 ]
Devine, Ryan [1 ]
Sein, Nancy [2 ]
George, Benjamin [1 ]
机构
[1] San Antonio Mil Med Ctr, Dept Hematol Oncol, Ft Sam Houston, TX 78234 USA
[2] San Antonio Mil Med Ctr, Dept Internal Med, Ft Sam Houston, TX 78234 USA
关键词
Renal cell carcinoma; Pazopanib; Axitinib; Everolimus; Temsirolimus; Tyrosine kinase inhibitors; Mammalian target of rapamycin inhibitors; PHASE-I TRIAL; ANTITUMOR-ACTIVITY; MAMMALIAN TARGET; RAPAMYCIN; EVEROLIMUS; PAZOPANIB; CANCER; INHIBITOR; AXITINIB; SURVIVAL;
D O I
10.1007/s11523-013-0303-8
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Prior to 2005, the treatment options for metastatic renal cell carcinoma (mRCC) were limited. There has been a proliferation of agents since the introduction of sorafenib, sunitinib, and becavicumab for clinical use in advanced renal cell carcinoma. Recently, four new agents have been approved by the US Food and Drug Administration (FDA) for use in mRCC. These agents come from two unique targeted pathways for RCC, tyrosine kinase inhibitors (TKIs) of vascular endothelial growth factor (VEGF) and mammalian target of rapamycin (mTOR) inhibitors. This review examines the investigational evolution, phases of development, adverse event profiles, and future directions of pazopanib, axitinib, everolimus, and temsirolimus as well as new novel agents being explored in clinical trials for these targeted pathways.
引用
收藏
页码:183 / 193
页数:11
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