首页> 外文期刊>International Journal of Cancer =: Journal International du Cancer >Progression-free survival and one-year milestone survival as surrogates for overall survival in previously treated advanced non-small cell lung cancer
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Progression-free survival and one-year milestone survival as surrogates for overall survival in previously treated advanced non-small cell lung cancer

机译:无进展的生存和一年的里程碑存活作为先前治疗的晚期非小细胞肺癌的整体生存替代品

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The advent of immunotherapy leads to greater availability of effective subsequent treatments and extended survival in previously treated advanced non-small cell lung cancer (NSCLC), complicating the evaluation of overall survival (OS) in second-line NSCLC trials. Here, we aimed to assess the surrogacy of progression-free survival (PFS) and milestone survival for OS in second-line NSCLC trials investigating chemotherapy, targeted therapy and immunotherapy, respectively. We systemically searched for active-controlled, second-line NSCLC trials. The milestone time point was set at one-year based on pre-analysis. A two-stage meta-analytic validation model was adopted to assess associations between surrogate endpoint (SE) and OS and associations between treatment effects on SE and OS. Treatment effects on SE and OS were expressed as PFS hazard ratios (HRPFS), 1 yr-milestone ratio (Ratio(1y-SUR)) and HROS. Subgroup analyses stratified by treatment types and trial publication years evaluated the surrogacy in different clinical contexts. The study included 50 trials with 22,804 patients. One-year survival strongly correlated with OS (R-2[95% confidence interval]: one-year survival -median OS = 0.707 [0.704-0.708]; Ratio(1y-SUR)-HROS = 0.829 [0.828-0.831]). No correlation was established between PFS and OS (median PFS-median OS = 0.100 [0.098-0.101]; HRPFS-HROS = 0.064 [0.059-0.069]), except in immunotherapy subgroup (HRPFS-HROS = 0.835 [0.791-0.918]). In subgroup analyses, surrogacy of one-year survival persisted in different clinical contexts, and the disassociation between PFS and OS persisted in recent trials. One-year milestone survival showed strong surrogacy for OS in second-line NSCLC trials. Although no association was identified between PFS and OS, the strong HRPFS-HROS correlation in immunotherapy trials indicates the potential of PFS as a SE in NSCLC trials involving immunotherapies.
机译:免疫疗法的出现导致有效的随后治疗的更大可用性,并在先前治疗的晚期非小细胞肺癌(NSCLC)中延长生存,使其在二线NSCLC试验中的整体存活(OS)的评估复杂化。在这里,我们旨在分别评估分别调查化疗,有针对性治疗和免疫疗法的二线NSCLC试验中的无进展生存期(PFS)和里程碑存活的替代性。我们系统性地搜索了主动控制的第二行NSCLC试验。基于预分析的一年内设定了里程碑时间点。采用了两阶段元分析验证模型来评估代理终点(SE)和OS和OS与治疗效果的关联之间的关联。 SE和OS的治疗效果表达为PFS危险比(HRPF),1年 - 里程碑比(比率(1Y-SUR))和HROS。通过治疗类型和试验公开年分层分层的亚组分析评估了不同临床环境中的代孕。该研究包括50名试验,患者22,804名。一年生存与OS强烈相关(R-2 [95%置信区间]:一年生存--Median OS = 0.707 [0.704-0.708];比率(1Y-SUR)-HROS = 0.829 [0.828-0.831]) 。在PFS和OS之间没有建立相关性(中位数 - 中位数OS = 0.100 [0.098-0.101];除免疫疗法亚组外,HRPFS-HROS = 0.064)(HRPFS-HROS = 0.835 [0.791-0.918])除外。在亚组分析中,在不同的临床环境中持续的一年存活的替代物,并且在最近的试验中持续存在PFS和OS之间的解剖。一年的里程碑生存在二线NSCLC试验中表现出对OS的强烈代理。尽管PFS和OS之间没有鉴定关联,但免疫疗法试验中的强HRPFS-HRO相关性表明PFS在涉及免疫治疗中的NSCLC试验中的PFS。

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