Scaling and interpreting treatment effects in clinical trials using restricted mean survival time.

IF 2.2 3区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL Clinical Trials Pub Date : 2024-06-13 DOI:10.1177/17407745241254995
Theodore Karrison, Chen Hu, James Dignam
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Abstract

Background: Restricted mean survival time is the expected duration of survival up to a chosen time of restriction τ. For comparison studies, the difference in restricted mean survival times between two groups provides a summary measure of the treatment effect that is free of assumptions regarding the relative shape of the two survival curves, such as proportional hazards. However, it can be difficult to judge the magnitude of the effect from a comparison of restricted means due to the truncation of observation at time τ.

Methods: In this article, we describe additional ways of expressing the treatment effect based on restricted means that can be helpful in this regard. These include the ratio of restricted means, the ratio of life-years (or time) lost, and the average integrated difference between the survival curves, equal to the difference in restricted means divided by τ. These alternative metrics are straightforward to calculate and provide a means for scaling the effect size as an aid to interpretation. Examples from two randomized, multicenter clinical trials in prostate cancer, NRG/RTOG 0521 and NRG/RTOG 0534, with primary endpoints of overall survival and biochemical/radiological progression-free survival, respectively, are presented to illustrate the ideas.

Results: The four effect measures (restricted mean survival time difference, restricted mean survival time ratio, time lost ratio, and average survival rate difference) were 0.45 years, 1.05, 0.81, and 0.038 for RTOG 0521 and 1.36 years, 1.17, 0.56, and 0.12 for RTOG 0534 with τ = 12 and 11 years, respectively. Thus, for example, the 0.45-year difference in the first trial translates into a 19% reduction in time lost and a 3.8% average absolute difference between the survival curves over the 12-year horizon, a modest effect size, whereas the 1.36-year difference in the second trial corresponds to a 44% reduction in time lost and a 12% absolute survival difference, a rather large effect.

Conclusions: In addition to the difference in restricted mean survival times, these alternative measures can be helpful in determining whether the magnitude of the treatment effect is clinically meaningful.

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使用受限平均生存时间对临床试验中的治疗效果进行缩放和解释。
背景:对于比较研究而言,两组间受限平均生存时间的差异提供了一个治疗效果的概括衡量指标,它不需要对两组生存曲线的相对形状(如比例危险)进行假设。然而,由于在时间τ处的观察被截断,因此很难从受限平均值的比较中判断效果的大小:在本文中,我们介绍了基于受限均值来表示治疗效果的其他方法,这些方法在这方面可能会有所帮助。这些方法包括受限均值之比、损失的生命年(或时间)之比以及生存曲线之间的平均综合差异(等于受限均值之差除以τ)。本文以两项前列腺癌多中心随机临床试验(NRG/RTOG 0521 和 NRG/RTOG 0534)为例,分别以总生存期和无生化/放射进展生存期为主要终点,来说明上述观点:RTOG 0521 的四个效应指标(受限平均生存时间差、受限平均生存时间比、时间损失比和平均生存率差)分别为 0.45 年、1.05 年、0.81 年和 0.038 年,RTOG 0534 的四个效应指标(τ = 12 年和 11 年)分别为 1.36 年、1.17 年、0.56 年和 0.12 年。因此,举例来说,第一项试验中0.45年的差异相当于减少了19%的时间损失,12年生存曲线之间的平均绝对差异为3.8%,效应大小适中;而第二项试验中1.36年的差异相当于减少了44%的时间损失,12%的绝对生存差异,效应相当大:除了限制性平均生存时间的差异外,这些替代指标还有助于确定治疗效果的大小是否具有临床意义。
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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.
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