Discovery and development of sorafenib: a multikinase inhibitor for treating cancer

被引:1441
作者
Wilhelm, Scott [1 ]
Carter, Christopher [1 ]
Lynch, Mark [1 ]
Lowinger, Timothy [1 ]
Dumas, Jacques [1 ]
Smith, Roger A. [1 ]
Schwartz, Brian [1 ]
Simantov, Ronit [1 ]
Kelley, Susan [1 ]
机构
[1] Bayer Pharmaceut Corp, Dept Canc Res, West Haven, CT 06516 USA
关键词
D O I
10.1038/nrd2130
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Since the molecular revolution of the 1980s, knowledge of the aetiology of cancer has increased considerably, which has led to the discovery and development of targeted therapies tailored to inhibit cancer-specific pathways. The introduction and refinement of rapid, high-throughput screening technologies over the past decade has greatly facilitated this targeted discovery and development process. Here, we describe the discovery and continuing development of sorafenib ( previously known as BAY 43-9006), the first oral multikinase inhibitor that targets Raf and affects tumour signalling and the tumour vasculature. The discovery cycle of sorafenib (Nexavar; Bayer Pharmaceuticals) - from initial screening for a lead compound to FDA approval for the treatment of advanced renal cell carcinoma in December 2005 - was completed in just 11 years, with approval being received similar to 5 years after the initiation of the first Phase I trial.
引用
收藏
页码:835 / 844
页数:10
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