成分删减复合终点的统计方法。

IF 2.2 3区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL Clinical Trials Pub Date : 2024-10-01 Epub Date: 2024-08-08 DOI:10.1177/17407745241265628
Anne Eaton
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引用次数: 0

摘要

复合终点定义为两个或两个以上事件最早发生的时间,在临床试验中常被用作主要终点。当综合终点的不同组成部分采用不同的剔除方式时,就会出现成分剔除。我们重点研究死亡和非致命事件的复合终点,其中死亡时间采用右侧剔除,而非致命事件时间采用区间剔除,因为只有在研究访问期间才能检测到该事件。此类数据通常使用右删减数据的方法进行分析,将首次检测到非致命事件的时间视为事件发生的时间。这可能会导致偏差,尤其是当评估间隔时间较长时。我们介绍了几种估算无事件生存曲线的方法,以及通过危险比估算治疗对无事件生存的影响的方法,这些方法是专门为处理成分删减而设计的。我们将这些方法应用到一项随机研究中,研究对象是感染人类免疫缺陷病毒的母亲所生的婴儿,研究方法是母乳喂养还是配方奶粉喂养。
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Statistical approaches for component-wise censored composite endpoints.

Composite endpoints defined as the time to the earliest of two or more events are often used as primary endpoints in clinical trials. Component-wise censoring arises when different components of the composite endpoint are censored differently. We focus on a composite of death and a non-fatal event where death time is right censored and the non-fatal event time is interval censored because the event can only be detected during study visits. Such data are most often analysed using methods for right censored data, treating the time the non-fatal event was first detected as the time it occurred. This can lead to bias, particularly when the time between assessments is long. We describe several approaches for estimating the event-free survival curve and the effect of treatment on event-free survival via the hazard ratio that are specifically designed to handle component-wise censoring. We apply the methods to a randomized study of breastfeeding versus formula feeding for infants of mothers infected with human immunodeficiency virus.

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来源期刊
Clinical Trials
Clinical Trials 医学-医学:研究与实验
CiteScore
4.10
自引率
3.70%
发文量
82
审稿时长
6-12 weeks
期刊介绍: Clinical Trials is dedicated to advancing knowledge on the design and conduct of clinical trials related research methodologies. Covering the design, conduct, analysis, synthesis and evaluation of key methodologies, the journal remains on the cusp of the latest topics, including ethics, regulation and policy impact.
期刊最新文献
Challenges in conducting efficacy trials for new COVID-19 vaccines in developed countries. Society for Clinical Trials Data Monitoring Committee initiative website: Closing the gap. A comparison of computational algorithms for the Bayesian analysis of clinical trials. Comparison of Bayesian and frequentist monitoring boundaries motivated by the Multiplatform Randomized Clinical Trial. Efficient designs for three-sequence stepped wedge trials with continuous recruitment.
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