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Noninferiority trials in second-line treatments of nonsmall cell lung cancer: A systematic review of literature with meta-analysis of phase III randomized clinical trials

机译:非小细胞肺癌二线治疗中的非劣效性试验:对III期随机临床试验进行荟萃分析的文献综述

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BACKGROUND:: To assess the role of the novel second-line treatments in nonsmall cell lung cancer (NSCLC). METHODS:: A systematic review of the literature with meta-analysis of phase III randomized clinical trials (RCTs) was independently performed by 3 authors. All the trials comparing any novel treatment with every-3-weeks docetaxel (3WD) and designed as noninferiority trial were included in the analysis. One-year survival rate (SR) was the primary end point, and quality of life and safety represented the secondary end points. RESULTS:: Four RCTs met the selection criteria. The outcomes of 3355 patients were analyzed in the pooled analysis. No heterogeneity was documented in the primary analysis either including all the trials or analyzing separately gefitinib and the chemotherapeutic alternatives to 3WD. The cumulative odds ratio was 0.927 (P=0.313) for 1-year SR, 0.889 (P=0.323) for the chemotherapeutic alternatives to 3WD and 0.953 (P=0.616) for gefitinib. The experimental arms showed a significant advantage in quality of life in the cumulative analysis (odds ratio=1.623, P=0.01) and in the subgroup of patients treated with gefitinib (odds ratio=1.962, P<0.001); a better safety profile for the experimental arm was observed in the cumulative analysis and in the subgroups of alternative chemotherapies or gefitinib. CONCLUSION:: All the noninferiority trials demonstrated the noninferiority of pemetrexed, oral topotecan, or gefitinib in 1-year SR (primary end point), but the improvement in overall survival remains modest. The improvement in quality of life and safety (secondary end points) represents the main value of these treatments, whose aim is mainly palliative.
机译:背景::评估新型二线治疗在非小细胞肺癌(NSCLC)中的作用。方法:由3位作者独立进行了对III期随机临床试验(RCT)的荟萃分析的文献综述。分析中包括所有将每3周多西紫杉醇(3WD)与任何新型治疗进行比较并设计为非劣效性试验的试验。一年生存率(SR)是主要终点,生活质量和安全性是次要终点。结果:四个RCT符合选择标准。在汇总分析中分析了3355例患者的结局。包括所有试验或单独分析吉非替尼和3WD化疗替代方案的主要分析均未记录异质性。一年期SR的累积比值比为0.927(P = 0.313),对于3WD的化疗替代药物,吉非替尼的累积比值比为0.889(P = 0.323)。实验组在累积分析(优势比= 1.623,P = 0.01)和接受吉非替尼治疗的患者亚组中(优势比= 1.962,P <0.001)在生活质量上显示出显着优势;在累积分析以及替代化学疗法或吉非替尼的亚组中,观察到了更好的安全性。结论:所有非劣效性试验均证明培美曲塞,口服拓扑替康或吉非替尼在1年SR(主要终点)中具有非劣效性,但总体生存率的改善仍然不大。生活质量和安全性的改善(次级终点)代表了这些治疗方法的主要价值,其主要目的是姑息治疗。

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