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mTOR抑制剂:坦西莫司和依维莫司治疗肾细胞癌

[mTOR inhibitors: temsirolimus and everolimus in the treatment of renal cell carcinoma].

作者信息

Ravaud A, Bernhard J-C, Gross-Goupil M, Digue L, Ferriere J-M

机构信息

CHU de Bordeaux, hôpital Saint-André, Service d'oncologie médicale, 1, rue Jean-Burguet, 33000 Bordeaux, France.

出版信息

Bull Cancer. 2010;97:45-51. doi: 10.1684/bdc.2010.1069.

Abstract

mTOR signaling pathway (mammalian target of rapamycin) is a major pathway in cell physiology and malignant behavior implicated in cell growth, cell proliferation, cell metabolism, protein synthesis and angiogenesis. Temsirolimus has shown in a randomized phase III trial for patients with poor risk feature of metastatic renal cell carcinoma, a significant gain in overall survival compared to this obtained with alpha interferon (7.3 à 10.9 months; HR: 0.73; P < 0.0069). Everolimus has shown in a randomized phase III trial for patients with metastatic renal cell carcinoma having failed under VEGFR tyrosine kinase inhibitor a significant gain in progression-free survival compared to this obtained with placebo VEGFR (1,8 à 4,6 months; HR: 0.33; P < 0.001). Temsirolimus and everolimus are now part of the reference treatments in renal cell carcinoma. This paper is a review of these two drugs in this setting.

摘要

mTOR信号通路(哺乳动物雷帕霉素靶蛋白)是细胞生理学和恶性行为中的一条主要通路,涉及细胞生长、细胞增殖、细胞代谢、蛋白质合成和血管生成。替西罗莫司在一项针对转移性肾细胞癌风险特征较差患者的随机III期试验中显示,与α干扰素相比,总生存期有显著提高(7.3至10.9个月;风险比:0.73;P<0.0069)。依维莫司在一项针对接受VEGFR酪氨酸激酶抑制剂治疗失败的转移性肾细胞癌患者的随机III期试验中显示,与安慰剂VEGFR相比,无进展生存期有显著提高(1.8至4.6个月;风险比:0.33;P<0.001)。替西罗莫司和依维莫司现在是肾细胞癌参考治疗方案的一部分。本文是对这两种药物在这种情况下的综述。

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