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Trends in phase III randomized controlled clinical trials on the treatment of advanced non‐small‐cell lung cancer

机译:晚期非小细胞肺癌治疗的III期随机对照临床试验的趋势

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摘要

The objective of this review was to analyze trends in outcomes and in the quality of phase III randomized controlled trials on advanced NSCLC published between 2000 and 2012, selecting 76 trials from a total of 122 retrieved in a structured search. Over the study period, the number of randomized patients per trial increased by 14 per year (P = 0.178). The sample size significantly increased between 2000 and 2012 in trials of targeted agents (460.1 vs. 740.8 patients, P = 0.009), trials of >1 drug (360.4 vs. 584.8, P = 0.014), and those including patients with good performance status (675.3 vs. 425.6; P = 0.003). Quality of life was assessed in 46 trials (60.5%), and significant improvements were reported in 10 of these (21.7%). Platinum‐based regimens were the most frequently investigated (86.8% of trials). Molecular‐targeted agents were studied in 25.0% of chemotherapy arms, and the percentage of trials including these agents increased each year. The median (interquartile range) overall survival (MOS) was 9.90 (3.5) months with an increase of 0.384 months per year of publication (P < 0.001). A statistically significant improvement in MOS was obtained in only 13 (18.8%) trials. The median progression‐free survival was 4.9 (1.9) months, with a nonsignificant increase of 0.026 months per year (P > 0.05). There has been a continuous but modest improvement in the survival of patients with advanced NSCLC over the past 12 years. Nevertheless, the quality of clinical trials and the benefit in outcomes should be carefully considered before the incorporation of novel approaches into clinical practice.
机译:这篇综述的目的是分析2000年至2012年间发表的晚期NSCLC的III期随机对照试验的结果和质量趋势,从结构化检索的122篇文献中选择76篇。在研究期间,每个试验的随机患者人数每年增加14(P = 0.178)。在2000年至2012年之间,针对靶向药物的试验(460.1 vs.740.8患者,P = 0.009),> 1种药物试验(360.4 vs.584.8,P = 0.014)以及包括表现良好患者的样本量显着增加(675.3与425.6; P = 0.003)。在46项试验中评估了生活质量(60.5%),其中10项报告了显着改善(21.7%)。铂类方案是研究最频繁的方案(试验的86.8%)。分子靶向药物在25.0%的化疗组中得到了研究,包括这些药物的试验百分比逐年增加。中位(四分位间距)总体生存期(MOS)为9.90(3.5)个月,每年出版量增加0.384个月(P <0.001)。仅13个试验(18.8%)获得了MOS的统计学显着改善。无进展生存期中位数为4.9(1.9)个月,每年无明显增加0.026个月(P> 0.05)。在过去的12年中,晚期NSCLC患者的生存率一直持续但适度提高。尽管如此,在将新方法纳入临床实践之前,应仔细考虑临床试验的质量和结果的益处。

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