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激酶抑制剂在肾细胞癌治疗中的应用

Kinase inhibitors in the treatment of renal cell carcinoma.

作者信息

Larkin James M G, Eisen Tim

机构信息

Department of Medicine, Royal Marsden Hospital, Downs Road, Sutton, Surrey SM2 5PT, UK.

出版信息

Crit Rev Oncol Hematol. 2006 Dec;60(3):216-26. doi: 10.1016/j.critrevonc.2006.06.008. Epub 2006 Jul 24.

Abstract

Immunotherapy confers a small but significant overall survival advantage in metastatic renal cell carcinoma (RCC) but a need exists to develop more effective systemic therapies. Angiogenesis has a key role in the pathophysiology of renal cell carcinoma and vascular endothelial growth factor (VEGF) is an important mediator of this process. Sunitinib, sorafenib and axitinib are new agents which belong to a class of drugs called kinase inhibitors and inhibit the VEGF, platelet-derived growth factor (PDGF) and c-KIT receptor tyrosine kinases. Temsirolimus inhibits the mammalian target of rapamycin (mTOR). All these agents have shown significant activity with manageable toxicity in metastatic RCC in phase 2 studies in patients generally pretreated with immunotherapy, whilst prolonged progression-free survival in a phase 3 study has been reported with sorafenib in comparison with placebo. Further phase 3 trials are recruiting and the combination of kinase inhibitors with other therapies is under investigation.

摘要

免疫疗法在转移性肾细胞癌(RCC)中可带来虽小但显著的总生存优势,但仍需要开发更有效的全身治疗方法。血管生成在肾细胞癌的病理生理学中起关键作用,血管内皮生长因子(VEGF)是这一过程的重要介质。舒尼替尼、索拉非尼和阿昔替尼是一类名为激酶抑制剂的新型药物,可抑制VEGF、血小板衍生生长因子(PDGF)和c-KIT受体酪氨酸激酶。替西罗莫司可抑制哺乳动物雷帕霉素靶蛋白(mTOR)。在通常接受过免疫治疗的患者中进行的2期研究表明,所有这些药物在转移性RCC中均显示出显著活性且毒性可控,而与安慰剂相比,索拉非尼在3期研究中报告了更长的无进展生存期。进一步的3期试验正在招募患者,激酶抑制剂与其他疗法的联合应用也在研究中。

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