{"title":"A new method for dealing with collider bias in the PWP model for recurrent events in randomized controlled trials.","authors":"Chen Shi, Jia-Wei Wei, Zi-Shu Zhan, Xiao-Han Xu, Ze-Lin Yan, Chun-Quan Ou","doi":"10.1186/s12874-025-02596-0","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Evaluating recurrent events within a time-to-event analysis framework effectively utilizes all relevant information to address the clinical question of interest fully and has certain advantages in randomized controlled trials (RCTs). However, the Prentice, Williams, and Peterson (PWP) model disrupts the randomness of the risk set for subsequent recurrent events other than the first and consequently introduces bias in estimating effects. This study aimed to propose a weighted PWP model, evaluate its statistical performance, and assess the potential consequences of using common practices when each recurrence has different baseline hazard functions.</p><p><strong>Methods: </strong>We proposed adjusting the estimate of treatment effect through a weighting strategy that constructed a virtual population balanced between groups in each risk set. A simulation study was carried out. The characteristic of the simulation data was the baseline hazard changed with the number of events. The proposed weighted PWP model was compared with current methods, including Cox for time-to-first-event, Poisson, negative binomial (NB), Andersen-Gill (AG), Lin-Wei-Yang-Ying (LWYY), and PWP models. Model performance was evaluated by bias, type I error rates, and statistical power. All models were applied to a real case from a randomization trial of Chemoprophylaxis treatment for Recurrent Stage I Bladder Tumors.</p><p><strong>Results: </strong>The results showed that the proposed weighted PWP model performed best with the lowest bias and highest statistical power. However, other models, including the Cox for time-to-first-event, Poisson, NB, AG, LWYY, and PWP models, all showed different degrees of bias and inflated type I error rates or low statistical power in the case of the baseline hazard changed with the number of events. Covariate adjustment via outcome regression can lead to inflated type I error rates. When the number of recurrent events was restricted, all weighting strategies yielded stable and nearly consistent results.</p><p><strong>Conclusions: </strong>Recurrent event data should be analyzed with caution. The proposed methods may be generalized to model recurrent events. Our findings serve as an important clarification of how to deal with collider bias in the PWP model in RCTs.</p>","PeriodicalId":9114,"journal":{"name":"BMC Medical Research Methodology","volume":"25 1","pages":"142"},"PeriodicalIF":3.9000,"publicationDate":"2025-05-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12105184/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"BMC Medical Research Methodology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1186/s12874-025-02596-0","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"HEALTH CARE SCIENCES & SERVICES","Score":null,"Total":0}
引用次数: 0
Abstract
Background: Evaluating recurrent events within a time-to-event analysis framework effectively utilizes all relevant information to address the clinical question of interest fully and has certain advantages in randomized controlled trials (RCTs). However, the Prentice, Williams, and Peterson (PWP) model disrupts the randomness of the risk set for subsequent recurrent events other than the first and consequently introduces bias in estimating effects. This study aimed to propose a weighted PWP model, evaluate its statistical performance, and assess the potential consequences of using common practices when each recurrence has different baseline hazard functions.
Methods: We proposed adjusting the estimate of treatment effect through a weighting strategy that constructed a virtual population balanced between groups in each risk set. A simulation study was carried out. The characteristic of the simulation data was the baseline hazard changed with the number of events. The proposed weighted PWP model was compared with current methods, including Cox for time-to-first-event, Poisson, negative binomial (NB), Andersen-Gill (AG), Lin-Wei-Yang-Ying (LWYY), and PWP models. Model performance was evaluated by bias, type I error rates, and statistical power. All models were applied to a real case from a randomization trial of Chemoprophylaxis treatment for Recurrent Stage I Bladder Tumors.
Results: The results showed that the proposed weighted PWP model performed best with the lowest bias and highest statistical power. However, other models, including the Cox for time-to-first-event, Poisson, NB, AG, LWYY, and PWP models, all showed different degrees of bias and inflated type I error rates or low statistical power in the case of the baseline hazard changed with the number of events. Covariate adjustment via outcome regression can lead to inflated type I error rates. When the number of recurrent events was restricted, all weighting strategies yielded stable and nearly consistent results.
Conclusions: Recurrent event data should be analyzed with caution. The proposed methods may be generalized to model recurrent events. Our findings serve as an important clarification of how to deal with collider bias in the PWP model in RCTs.
背景:在事件时间分析框架内评估复发事件有效地利用所有相关信息来充分解决感兴趣的临床问题,并且在随机对照试验(rct)中具有一定的优势。然而,Prentice, Williams, and Peterson (PWP)模型破坏了除第一次事件外后续复发事件风险集的随机性,因此在估计效果时引入了偏差。本研究旨在提出一个加权的PWP模型,评估其统计性能,并评估当每次复发具有不同的基线危险函数时使用常见做法的潜在后果。方法:我们提出通过加权策略调整治疗效果的估计,该策略在每个风险集的组之间构建了一个虚拟人群平衡。进行了仿真研究。模拟数据的特点是基线危险度随事件数量的变化而变化。将所提出的加权PWP模型与现有方法进行比较,包括Cox for time-to-first-event、Poisson、负二项(NB)、Andersen-Gill (AG)、Lin-Wei-Yang-Ying (LWYY)和PWP模型。通过偏倚、I型错误率和统计功率来评估模型的性能。所有的模型都被应用于一个真实的病例,这个病例来自于一项化疗预防治疗复发期膀胱肿瘤的随机试验。结果:所提出的加权PWP模型具有最小的偏差和最高的统计能力。然而,其他模型,包括Cox for time-to-first-event、Poisson、NB、AG、LWYY和PWP模型,在基线危害随事件数量变化的情况下,都表现出不同程度的偏差,I型错误率过高或统计能力较低。通过结果回归进行协变量调整可能导致I型错误率膨胀。当重复事件的数量受到限制时,所有加权策略都产生稳定且几乎一致的结果。结论:应谨慎分析复发事件资料。所提出的方法可以推广到重复事件的模型。我们的研究结果为如何处理随机对照试验中PWP模型中的对撞机偏差提供了重要的澄清。
期刊介绍:
BMC Medical Research Methodology is an open access journal publishing original peer-reviewed research articles in methodological approaches to healthcare research. Articles on the methodology of epidemiological research, clinical trials and meta-analysis/systematic review are particularly encouraged, as are empirical studies of the associations between choice of methodology and study outcomes. BMC Medical Research Methodology does not aim to publish articles describing scientific methods or techniques: these should be directed to the BMC journal covering the relevant biomedical subject area.