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转移性肾细胞癌的治疗选择:聚焦于 mTOR 抑制剂。

Treatment Options in Metastatic Renal Cell Carcinoma: Focus on mTOR Inhibitors.

机构信息

Department of Medical Oncology and Experimental Therapeutics, City of Hope Comprehensive Cancer Center, Duarte, CA, USA.

出版信息

Clin Med Insights Oncol. 2010 Jun 9;4:43-53. doi: 10.4137/cmo.s1590.

Abstract

THE AGENTS CURRENTLY APPROVED FOR USE IN METASTATIC RENAL CELL CARCINOMA (MRCC) CAN BE DIVIDED BROADLY INTO TWO CATEGORIES: (1) vascular endothelial growth factor receptor (VEGFR)-directed therapies or (2) inhibitors of the mammalian target of rapamycin (mTOR). The latter category includes everolimus and temsirolimus, both approved for distinct indications in mRCC. Everolimus gained its approval on the basis of phase III data showing a benefit in progression-free survival relative to placebo in patients previously treated with sunitinib and/or sorafenib. In contrast, temsirolimus was approved on the basis of a phase III trial in treatment-naïve patients with poor-risk mRCC, demonstrating an improvement in overall survival relative to interferon-alfa. While these pivotal trials have created unique positions for everolimus and temsirolimus in current clinical algorithms, the role of mTOR inhibitors in mRCC is being steadily revised and expanded through ongoing trials testing novel sequences and combinations. The clinical development of mTOR inhibitors is outlined herein.

摘要

目前批准用于转移性肾细胞癌(mRCC)的药物可大致分为两类:(1)血管内皮生长因子受体(VEGFR)靶向治疗药物,或(2)哺乳动物雷帕霉素靶蛋白(mTOR)抑制剂。后一类包括依维莫司和替西罗莫司,两者均因在 mRCC 中的不同适应证而获得批准。依维莫司基于 III 期数据获得批准,该数据显示与安慰剂相比,在先前接受舒尼替尼和/或索拉非尼治疗的患者中,无进展生存期有获益。相比之下,替西罗莫司基于 III 期试验在预后不良的 mRCC 初治患者中获得批准,与干扰素-α相比,总生存期有改善。虽然这些关键性试验为依维莫司和替西罗莫司在当前的临床方案中创造了独特的地位,但通过正在进行的试验测试新的序列和组合,mTOR 抑制剂在 mRCC 中的作用正在不断修订和扩展。本文概述了 mTOR 抑制剂的临床开发情况。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/98bd/2902205/0d47584eb9f5/cmo-2010-043f1.jpg

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