首页> 外文期刊>The Lancet >Maintenance pemetrexed plus best supportive care versus placebo plus best supportive care for non-small-cell lung cancer: a randomised, double-blind, phase 3 study.
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Maintenance pemetrexed plus best supportive care versus placebo plus best supportive care for non-small-cell lung cancer: a randomised, double-blind, phase 3 study.

机译:维护Pemetrexed Plus最佳支持性护理与安慰剂加上非小细胞肺癌最佳支持性护理:随机,双盲,第3期研究。

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BACKGROUND: Several studies have shown the efficacy, tolerability, and ease of administration of pemetrexed-an antifolate antineoplastic agent-in patients with advanced non-small-cell lung cancer. We assessed pemetrexed as maintenance therapy in patients with this disease. METHODS: This randomised double-blind study was undertaken in 83 centres in 20 countries. 663 patients with stage IIIB or IV disease who had not progressed on four cycles of platinum-based chemotherapy were randomly assigned (2:1 ratio) to receive pemetrexed (500 mg/m(2), day 1) plus best supportive care (n=441) or placebo plus best supportive care (n=222) in 21-day cycles until disease progression. Treatment was randomised with the Simon and Pocock minimisation method. Patients and investigators were masked to treatment. All patients received vitamin B(12), folic acid, and dexamethasone. The primary endpoint of progression-free survival and the secondary endpoint of overall survival were analysed by intention to treat. This study is registered with ClinicalTrials.gov, number NCT00102804. FINDINGS: All randomly assigned participants were analysed. Pemetrexed significantly improved progression-free survival (4.3 months [95% CI 4.1-4.7] vs 2.6 months [1.7-2.8]; hazard ratio [HR] 0.50, 95% CI 0.42-0.61, p<0.0001) and overall survival (13.4 months [11.9-15.9] vs 10.6 months [8.7-12.0]; HR 0.79, 0.65-0.95, p=0.012) compared with placebo. Treatment discontinuations due to drug-related toxic effects were higher in the pemetrexed group than in the placebo group (21 [5%] vs three [1%]). Drug-related grade three or higher toxic effects were higher with pemetrexed than with placebo (70 [16%] vs nine [4%]; p<0.0001), specifically fatigue (22 [5%] vs one [1%], p=0.001) and neutropenia (13 [3%] vs 0, p=0.006). No pemetrexed-related deaths occurred. Relatively fewer patients in the pemetrexed group than in the placebo group received systemic post-discontinuation therapy (227 [51%] vs 149 [67%]; p=0.0001). INTERPRETATION: Maintenance therapy with pemetrexed is well tolerated and offers improved progression-free and overall survival compared with placebo in patients with advanced non-small-cell lung cancer. FUNDING: Eli Lilly.
机译:背景:若干研究表明了磷酸术治疗患者的疗效,耐受性和施用磷酸盐抗血清抗肿瘤患者的疗效,耐受性和易于施用的疗效。我们评估了这种疾病患者的培养治疗。方法:在20个国家的83个中心进行了随机双盲研究。 663例患有IIIB阶段或IV疾病的患者随机分配(2:1的比例),以接受Pemetrexed(500mg / m(2),第1天)加上最佳支持护理(n = 441)或安慰剂加上21天循环中最佳的支持性护理(n = 222),直到疾病进展。用西蒙和Pocock最小化方法随机化。患者和调查人员被掩盖治疗。所有患者接受维生素B(12),叶酸和地塞米松。通过意图治疗分析无进展存活的主要终点和整体存活的次要终点。本研究以ClinicalTrials.gov注册,NCT00102804号码。调查结果:分析了所有随机分配的参与者。 Pemetrexed显着改善了无进展的存活(4.3个月[95%CI 4.1-4.7] Vs 2.6个月[1.7-2.8];危害比[HR] 0.50,95%CI 0.42-0.61,P <0.0001)和总体存活(13.4几个月[11.9-15.9]与10.6个月[8.7-12.0];与安慰剂相比,HR 0.79,0.65-0.95,P = 0.012)。在与药物相关的毒性作用引起的治疗中断率高于安慰剂组(21 [5%] Vs三[1%])。与PEMORDEXED相关的药物相关的三级或更高毒性效应(70 [16%]九[4%]; P <0.0001),特别疲劳(22 [5%] Vs [1%],p = 0.001)和中性蛋白(13 [3%] Vs 0,P = 0.006)。没有发生培养基相关的死亡。培养基群中相对较少的患者比安慰剂组在安慰剂组中获得全身停药后治疗(227 [51%] Vs 149 [67%]; P = 0.0001)。解释:具有培养基的维护治疗是良好的耐受性,与晚期非小细胞肺癌患者的安慰剂相比,提供了改善的无进展和整体存活。资金:Eli Lilly。

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