Third generation tyrosine kinase inhibitors and their development in advanced renal cell carcinoma

被引:31
|
作者
Bukowski, Ronald M. [1 ]
机构
[1] Cleveland Clin, Lerner Coll Med CWRU, Taussig Canc Ctr, Pepper Pike, OH USA
来源
FRONTIERS IN ONCOLOGY | 2012年 / 2卷
关键词
renal cell carcinoma; tyrosine kinase inhibitors;
D O I
10.3389/fonc.2012.00013
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Angiogenesis in general and the vascular endothelial growth factor (VEGF) signaling axis in particular is a validated target in renal cell carcinoma (RCC). Clear-cell carcinoma of the kidney is now recognized as a malignancy that is sensitive to inhibitors of the VEGF pathway. Treatment options for patients with metastatic renal cell carcinoma have evolved in dramatic fashion over the past 6 years, and a new paradigm has developed. The cytokines interferon a and interleukin-2 were previously utilized for therapy, but since December 2005, six new agents have been approved in the United States for the treatment of advanced RCC. Two are tyrosine kinase inhibitors (TKI's) including sunitinib and recently pazopanib, and the multikinase inhibitor sorafenib. The current review examines the evolving data with the next generation of TKI's, axitinib and tivozanib being developed for the treatment of advanced RCC. These agents were synthesized to provide increased target specificity and enhanced target inhibition. The preclinical and clinical data are examined, an overview of the development of these TKI's is provided, and discussion plus speculation concerning their potential roles as RCC therapy is provided.
引用
收藏
页数:10
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