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首页> 外文期刊>Statistics in medicine >Quantifying the totality of treatment effect with multiple event‐time observations in the presence of a terminal event from a comparative clinical study
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Quantifying the totality of treatment effect with multiple event‐time observations in the presence of a terminal event from a comparative clinical study

机译:在来自比较临床研究的终末事件存在下,在多个事件时间观测中量化治疗效果的整体性

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摘要

To evaluate the totality of one treatment's benefit/risk profile relative to an alternative treatment via a longitudinal comparative clinical study, the timing and occurrence of multiple clinical events are typically collected during the patient's follow‐up. These multiple observations reflect the patient's disease progression/burden over time. The standard practice is to create a composite endpoint from the multiple outcomes, the timing of the occurrence of the first clinical event, to evaluate the treatment via the standard survival analysis techniques. By ignoring all events after the composite outcome, this type of assessment may not be ideal. Various parametric or semiparametric procedures have been extensively discussed in the literature for the purposes of analyzing multiple event‐time data. Many existing methods were developed based on extensive model assumptions. When the model assumptions are not plausible, the resulting inferences for the treatment effect may be misleading. In this article, we propose a simple, nonparametric inference procedure to quantify the treatment effect, which has an intuitive clinically meaningful interpretation. We use the data from a cardiovascular clinical trial for heart failure to illustrate the procedure. A simulation study is also conducted to evaluate the performance of the new proposal.
机译:为了通过纵向比较临床研究评估相对于替代治疗的一个治疗的益处/风险轮廓的整体,通常在患者的随访期间收集多种临床事件的时序和发生。这些多种观察结果反映了患者的疾病进展/负担随着时间的推移。标准做法是从多重结果创建一个复合端点,第一临床事件发生的时间,以通过标准存活分析技术评估处理。通过忽略复合结果后的所有事件,这种评估可能不是理想的。在文献中已经广泛讨论了各种参数或半造型程序,以便分析多个事件时间数据。许多现有方法是基于广泛的模型假设开发的。当模型假设不符号时,所产生的治疗效果的推论可能是误导性的。在本文中,我们提出了一种简单的非参数推断程序,以量化治疗效果,这具有直观的临床有意义的解释。我们使用来自心血管临床试验的数据进行心力衰竭,以说明该程序。还进行了模拟研究以评估新提案的表现。

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