{"title":"Penalized Variable Selection for Joint AFT Random-Effect Model With Clustered Competing-Risks Data.","authors":"Lin Hao, Il Do Ha","doi":"10.1002/pst.70084","DOIUrl":null,"url":null,"abstract":"<p><p>Clustered competing-risks data often arise in clinical studies, such as multi-center clinical trials, where the occurrence of an event within a cluster hinders the observation of other types of events. The correlation resulting from clustering can be modeled using random effects. These competing-risks data have usually been analyzed using hazard-based models, rather than survival times themselves. Hao et al. proposed a cause-specific joint accelerated failure time (AFT) random-effect modeling approach for analyzing the clustered competing-risks data, which is easy to interpret. In this article, we propose a variable selection method for fixed effects using a penalized h-likelihood (HL) procedure in the joint AFT competing-risk model. Simulation studies were conducted to evaluate the performance of the proposed variable selection procedure, which concluded that the penalized methods of SCAD and HL are more appropriate than that of LASSO. The proposed method is illustrated with two real clinical datasets.</p>","PeriodicalId":19934,"journal":{"name":"Pharmaceutical Statistics","volume":"25 2","pages":"e70084"},"PeriodicalIF":1.5000,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12989290/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Pharmaceutical Statistics","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1002/pst.70084","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
引用次数: 0
Abstract
Clustered competing-risks data often arise in clinical studies, such as multi-center clinical trials, where the occurrence of an event within a cluster hinders the observation of other types of events. The correlation resulting from clustering can be modeled using random effects. These competing-risks data have usually been analyzed using hazard-based models, rather than survival times themselves. Hao et al. proposed a cause-specific joint accelerated failure time (AFT) random-effect modeling approach for analyzing the clustered competing-risks data, which is easy to interpret. In this article, we propose a variable selection method for fixed effects using a penalized h-likelihood (HL) procedure in the joint AFT competing-risk model. Simulation studies were conducted to evaluate the performance of the proposed variable selection procedure, which concluded that the penalized methods of SCAD and HL are more appropriate than that of LASSO. The proposed method is illustrated with two real clinical datasets.
期刊介绍:
Pharmaceutical Statistics is an industry-led initiative, tackling real problems in statistical applications. The Journal publishes papers that share experiences in the practical application of statistics within the pharmaceutical industry. It covers all aspects of pharmaceutical statistical applications from discovery, through pre-clinical development, clinical development, post-marketing surveillance, consumer health, production, epidemiology, and health economics.
The Journal is both international and multidisciplinary. It includes high quality practical papers, case studies and review papers.