Molecular basis for sunitinib efficacy and future clinical development

被引:593
作者
Faivre, Sandrine
Demetri, George
Sargent, William
Raymond, Eric
机构
[1] Hop Beaujon, APHP, SIHC, Beaujon Bichat & RayLab, F-92118 Clichy, France
[2] Denis Diderot Univ, F-92118 Clichy, France
[3] Ludwig Ctr Dana Farber Harvard, Dana Farber Canc Inst, Ctr Sarcoma & Bone Oncol, Boston, MA 02115 USA
[4] Pfizer Inc, New York, NY 10017 USA
关键词
D O I
10.1038/nrd2380
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
Sunitinib malate (SU11248/ Sutent; Pfizer) is a multitargeted tyrosine kinase inhibitor that has potent anti-angiogenic and antitumour activities. Definitive efficacy has been demonstrated in advanced renal cell carcinoma and in gastrointestinal stromal tumours that are refractory or intolerant to imatinib (Gleevec; Novartis), which has provided the basis for the recent regulatory approvals for these indications. This article summarizes the discovery and development of sunitinib, and discusses key issues for the multitargeted approach in cancer treatment, such as markers of response and development of resistance, and their significance for the future development of sunitinib and other multikinase inhibitors.
引用
收藏
页码:734 / 745
页数:12
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