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Correlations of survival with progression-free survival, response rate, and disease control rate in advanced biliary tract cancer: a meta-analysis of randomised trials of first-line chemotherapy

机译:晚期胆道癌生存率与无进展生存率,缓解率和疾病控制率的相关性:一线化疗随机试验的荟萃分析

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摘要

Background: The need to promote novel drug development for advanced biliary tract cancer (ABTC) has emphasised the importance of determining whether various efficacy end points can act as surrogates for overall survival (OS).Methods: We conducted a literature search of randomised trials of first-line chemotherapy for ABTC and investigated correlations between efficacy end points and OS using weighted linear regression analysis. The ratios of the median OS, median progression-free survival (PFS), response rate, and disease control rate in each trial were used to summarise treatment effects. The surrogate threshold effect (STE), which was the minimum treatment effect on PFS required to predict a non-zero treatment effect on OS, was calculated.Results: Seventeen randomised trials with 36 treatment arms were identified, and a sample size of 2148 patients with 19 paired arms was analysed. The strongest correlation between all evaluated efficacy end points was observed between median OS and median PFS ratios (r2=0.66). In trials with gemcitabine-containing therapies and targeted agents, the r2-values were 0.78. The STE was estimated at 0.83 for all trials and 0.81 for trials with gemcitabine-containing therapies, and was not calculated for trials with targeted agents.Conclusions: The median PFS ratio correlated well with the median OS ratio, and may be useful for planning a clinical trial for novel drug development.
机译:背景:促进晚期胆道癌(ABTC)的新药开发的需求强调了确定各种功效终点是否可以作为整体生存(OS)的替代方法的重要性。方法:我们对以下文献进行了随机对照研究: ABTC的一线化疗,并使用加权线性回归分析研究了功效终点与OS之间的相关性。在每个试验中,中位OS​​,中位无进展生存期(PFS),缓解率和疾病控制率的比率用于总结治疗效果。计算了替代阈值效应(STE),它是预测PFS对OS的非零治疗效果所需的最小治疗效果。结果:确定了17个随机试验,共36个治疗组,样本量为2148例用19个配对的手臂进行了分析。在中位OS和中位PFS比之间观察到所有评估的功效终点之间最强的相关性(r2 = 0.66)。在含吉西他滨的疗法和靶向药物的试验中,r2值为0.78。所有试验的STE估计为0.83,含吉西他滨的试验的STE估计为0.81,未针对靶向药物的试验进行计算。结论:中位PFS比率与中位OS比率具有很好的相关性,可能对计划新药开发的临床试验。

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