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哺乳动物雷帕霉素靶蛋白(mTOR)抑制剂治疗肾癌的未来方向。

Future directions of mammalian target of rapamycin (mTOR) inhibitor therapy in renal cell carcinoma.

机构信息

Division of Genitourinary Malignancies, Department of Medical Oncology & Experimental Therapeutics, City of Hope Comprehensive Cancer Center, Los Angeles, CA, USA.

出版信息

Target Oncol. 2011 Mar;6(1):5-16. doi: 10.1007/s11523-011-0172-y. Epub 2011 Apr 12.

Abstract

With an explosion of available treatments for metastatic renal cell carcinoma (mRCC) in recent years, it is important to recognize that approved targeted therapies fall broadly into only two mechanistic categories. The first category, vascular endothelial growth factor (VEGF)-directed therapies, includes sunitinib, pazopanib, sorafenib and bevacizumab. The second category includes inhibitors of the mammalian target of rapamycin (mTOR), namely everolimus and temsirolimus. A pivotal trial of everolimus supports use of the agent in patients with mRCC refractory to VEGF- tyrosine kinase inhibitors (TKI) therapy, while pivotal data for temsirolimus supports use in poor-prognosis patients as first-line therapy. Multiple reviews exist to delineate the laboratory and clinical development of mTOR inhibitors. This paper will outline the future applications of these therapies. It will explore ongoing trials evaluating combinations of mTOR inhibitors with other targeted therapies, along with sequencing strategies and biomarker discovery efforts. The application of mTOR inhibitors in unique populations is also described.

摘要

近年来,转移性肾细胞癌 (mRCC) 的治疗方法大量涌现,因此必须认识到,已批准的靶向治疗药物主要可分为两类作用机制。第一类是血管内皮生长因子 (VEGF) 靶向治疗药物,包括舒尼替尼、帕唑帕尼、索拉非尼和贝伐珠单抗。第二类是哺乳动物雷帕霉素靶蛋白 (mTOR) 抑制剂,即依维莫司和替西罗莫司。一项关于依维莫司的关键性试验支持将该药物用于对 VEGF-酪氨酸激酶抑制剂 (TKI) 治疗耐药的 mRCC 患者,而关于替西罗莫司的关键性数据支持将其用于预后不良的患者作为一线治疗药物。目前已有多项综述详细阐述了 mTOR 抑制剂的实验室和临床开发情况。本文将概述这些治疗药物的未来应用。它将探讨正在进行的临床试验,评估 mTOR 抑制剂与其他靶向治疗药物的联合应用,以及测序策略和生物标志物发现工作。本文还描述了 mTOR 抑制剂在特殊人群中的应用。

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