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Everolimus: in advanced renal cell carcinoma.

机译:依维莫司:晚期肾细胞癌。

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摘要

Everolimus is an orally administered, targeted therapy indicated for the treatment of advanced renal cell carcinoma. It inhibits the mammalian target of rapamycin, an integral component of multiple pathways involved in cell growth and proliferation. Median progression-free survival was significantly longer with everolimus 10 mg once daily than with placebo in both second interim (4.0 vs 1.9 months) and updated (4.9 vs 1.9 months) analyses of a randomized, double-blind, placebo-controlled, multicentre, phase III trial in patients with metastatic renal cell carcinoma that had progressed while receiving sunitinib and/or sorafenib treatment. At the second interim analysis, median overall survival was 8.8 months for placebo recipients; at this analysis, overall survival had not yet been reached for everolimus recipients. With regard to objective response at the second interim analysis, 64% of everolimus and 32% of placebo recipients had either a partial response (1% and 0%) or stable disease (63% and 32%). The tolerability profile of everolimus was largely manageable in the phase III trial, with most treatment-related adverse events being of grade 1 or 2 severity.
机译:依维莫司是一种口服给药的靶向疗法,可用于治疗晚期肾细胞癌。它抑制雷帕霉素的哺乳动物靶标,雷帕霉素是涉及细胞生长和增殖的多种途径的组成部分。在第二次中期(4.0 vs. 1.9个月)和更新(4.9 vs 1.9个月)的随机,双盲,安慰剂对照,多中心分析中,依维莫司10 mg每天一次的中位无进展生存期显着长于安慰剂,在接受舒尼替尼和/或索拉非尼治疗期间进展的转移性肾细胞癌患者的III期临床试验。在第二次中期分析中,安慰剂接受者的中位总生存期为8.8个月。在此分析中,依维莫司接受者的总体生存率尚未达到。关于第二次中期分析的客观反应,依维莫司的64%和安慰剂接受者的32%有部分反应(1%和0%)或疾病稳定(63%和32%)。在III期试验中,依维莫司的耐受性在很大程度上可控,大多数与治疗相关的不良事件的严重性为1级或2级。

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