Regression calibration for time-to-event outcomes: mitigating bias due to measurement error in real-world endpoints.

Q3 Mathematics
Epidemiologic Methods Pub Date : 2025-09-26 eCollection Date: 2025-01-01 DOI:10.1515/em-2025-0009
Benjamin Ackerman, Ryan W Gan, Youyi Zhang, Juned Siddique, James Roose, Jennifer L Lund, Janick Weberpals, Jocelyn R Wang, Craig S Meyer, Jennifer Hayden, Khaled Sarsour, Ashita S Batavia
{"title":"Regression calibration for time-to-event outcomes: mitigating bias due to measurement error in real-world endpoints.","authors":"Benjamin Ackerman, Ryan W Gan, Youyi Zhang, Juned Siddique, James Roose, Jennifer L Lund, Janick Weberpals, Jocelyn R Wang, Craig S Meyer, Jennifer Hayden, Khaled Sarsour, Ashita S Batavia","doi":"10.1515/em-2025-0009","DOIUrl":null,"url":null,"abstract":"<p><strong>Objectives: </strong>In drug development, there is increasing interest in leveraging real-world data (RWD) to augment trial data and generate evidence about treatment efficacy. However, comparing patient outcomes across trial and routine clinical care settings can be susceptible to bias, namely due to differences in how and when disease assessments occur. This can introduce measurement error in RWD relative to trial standards and lead to bias when comparing endpoints. We develop a novel statistical method, survival regression calibration (SRC), to mitigate measurement error bias in time-to-event RWD outcomes and improve inferences when combining trials with RWD in oncology.</p><p><strong>Methods: </strong>SRC extends upon existing regression calibration methods to address measurement error in time-to-event RWD outcomes. The method entails fitting separate Weibull regression models using trial-like ('true') and real-world-like ('mismeasured') outcome measures in a validation sample, and then calibrating parameter estimates in the full study according to the estimated bias in Weibull parameters. We evaluate performance of SRC under varying degrees of existing measurement error bias via simulation, and then illustrate how SRC can address measurement error when estimating median progression-free survival (mPFS) in newly diagnosed multiple myeloma RWD.</p><p><strong>Results: </strong>When measurement error exists between trial and real-world mPFS, SRC can effectively account for its resulting bias. SRC yields greater reduction in measurement error bias than standard regression calibration methods, due to its suitability for time-to-event outcomes.</p><p><strong>Conclusions: </strong>Outcome measurement error is important to address when combining trials and RWD, as it may lead to biased results. Our SRC method helps mitigate such bias, improving comparability between real-world and trial endpoints and strengthening evidence of treatment efficacy.</p>","PeriodicalId":37999,"journal":{"name":"Epidemiologic Methods","volume":"14 1","pages":"20250009"},"PeriodicalIF":0.0000,"publicationDate":"2025-09-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12464481/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Epidemiologic Methods","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1515/em-2025-0009","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"Q3","JCRName":"Mathematics","Score":null,"Total":0}
引用次数: 0

Abstract

Objectives: In drug development, there is increasing interest in leveraging real-world data (RWD) to augment trial data and generate evidence about treatment efficacy. However, comparing patient outcomes across trial and routine clinical care settings can be susceptible to bias, namely due to differences in how and when disease assessments occur. This can introduce measurement error in RWD relative to trial standards and lead to bias when comparing endpoints. We develop a novel statistical method, survival regression calibration (SRC), to mitigate measurement error bias in time-to-event RWD outcomes and improve inferences when combining trials with RWD in oncology.

Methods: SRC extends upon existing regression calibration methods to address measurement error in time-to-event RWD outcomes. The method entails fitting separate Weibull regression models using trial-like ('true') and real-world-like ('mismeasured') outcome measures in a validation sample, and then calibrating parameter estimates in the full study according to the estimated bias in Weibull parameters. We evaluate performance of SRC under varying degrees of existing measurement error bias via simulation, and then illustrate how SRC can address measurement error when estimating median progression-free survival (mPFS) in newly diagnosed multiple myeloma RWD.

Results: When measurement error exists between trial and real-world mPFS, SRC can effectively account for its resulting bias. SRC yields greater reduction in measurement error bias than standard regression calibration methods, due to its suitability for time-to-event outcomes.

Conclusions: Outcome measurement error is important to address when combining trials and RWD, as it may lead to biased results. Our SRC method helps mitigate such bias, improving comparability between real-world and trial endpoints and strengthening evidence of treatment efficacy.

时间到事件结果的回归校准:减轻现实世界终点测量误差造成的偏差。
目的:在药物开发中,人们对利用真实世界数据(RWD)来增加试验数据和产生有关治疗疗效的证据越来越感兴趣。然而,在试验和常规临床护理环境中比较患者结果可能容易产生偏差,即由于疾病评估的方式和时间的差异。这可能会在RWD中引入相对于试验标准的测量误差,并在比较终点时导致偏差。我们开发了一种新的统计方法,生存回归校准(SRC),以减轻时间-事件RWD结果的测量误差偏差,并在将肿瘤试验与RWD相结合时改善推断。方法:SRC扩展了现有的回归校准方法,以解决时间-事件RWD结果的测量误差。该方法需要在验证样本中使用类似试验(“真实”)和类似现实世界(“误测”)的结果测量来拟合单独的威布尔回归模型,然后根据威布尔参数的估计偏差校准整个研究中的参数估计。我们通过模拟评估SRC在不同程度的现有测量误差偏差下的性能,然后说明SRC如何在估计新诊断的多发性骨髓瘤RWD的中位无进展生存期(mPFS)时解决测量误差。结果:当试验和实际mPFS之间存在测量误差时,SRC可以有效地解释其产生的偏差。SRC比标准回归校准方法更能减少测量误差偏差,因为它适合于时间-事件结果。结论:当将试验与RWD相结合时,结果测量误差很重要,因为它可能导致结果偏倚。我们的SRC方法有助于减轻这种偏差,提高现实世界和试验终点之间的可比性,并加强治疗疗效的证据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Epidemiologic Methods
Epidemiologic Methods Mathematics-Applied Mathematics
CiteScore
2.10
自引率
0.00%
发文量
7
期刊介绍: Epidemiologic Methods (EM) seeks contributions comparable to those of the leading epidemiologic journals, but also invites papers that may be more technical or of greater length than what has traditionally been allowed by journals in epidemiology. Applications and examples with real data to illustrate methodology are strongly encouraged but not required. Topics. genetic epidemiology, infectious disease, pharmaco-epidemiology, ecologic studies, environmental exposures, screening, surveillance, social networks, comparative effectiveness, statistical modeling, causal inference, measurement error, study design, meta-analysis
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信