{"title":"Simulated treatment comparisons with jackknife pseudo values for estimating population-adjusted marginal treatment effects.","authors":"Sean Yiu, Kirsty Rhodes","doi":"10.1080/10543406.2026.2685277","DOIUrl":null,"url":null,"abstract":"<p><p>Matching-adjusted indirect comparisons (MAIC) and simulated treatment comparisons (STC) are commonly used for indirect treatment comparisons when patient-level data are available for some treatments but not others. However, MAIC can become inefficient when covariate overlap across trials is limited, and STC may fail to estimate marginal (population average) treatment effects required for health technology assessment when non-linear outcome models, such as logistic or survival models, are used. We propose a new STC approach to address these limitations. For settings where a linear model for the treatment effect can be assumed (e.g. log odds ratios or log hazard ratios), we propose to apply STC with jackknife pseudo values of the marginal treatment effect estimate as the dependent variable, rather than the observed outcomes. These pseudo values decompose the marginal treatment effect estimate into individual patient contributions, which can then be regressed on patient-level characteristics to predict marginal treatment effects in alternative target populations. We illustrate the approach using two worked examples involving non-linear outcome models. In simulated trials of continuous, binary, and time-to-event outcomes, the proposed approach showed less bias than traditional STC for non-linear outcome models, and had lower mean squared error than MAIC, both under correct and incorrect specification of baseline covariate functional forms.</p>","PeriodicalId":54870,"journal":{"name":"Journal of Biopharmaceutical Statistics","volume":" ","pages":"1-22"},"PeriodicalIF":1.3000,"publicationDate":"2026-06-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Biopharmaceutical Statistics","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1080/10543406.2026.2685277","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
Matching-adjusted indirect comparisons (MAIC) and simulated treatment comparisons (STC) are commonly used for indirect treatment comparisons when patient-level data are available for some treatments but not others. However, MAIC can become inefficient when covariate overlap across trials is limited, and STC may fail to estimate marginal (population average) treatment effects required for health technology assessment when non-linear outcome models, such as logistic or survival models, are used. We propose a new STC approach to address these limitations. For settings where a linear model for the treatment effect can be assumed (e.g. log odds ratios or log hazard ratios), we propose to apply STC with jackknife pseudo values of the marginal treatment effect estimate as the dependent variable, rather than the observed outcomes. These pseudo values decompose the marginal treatment effect estimate into individual patient contributions, which can then be regressed on patient-level characteristics to predict marginal treatment effects in alternative target populations. We illustrate the approach using two worked examples involving non-linear outcome models. In simulated trials of continuous, binary, and time-to-event outcomes, the proposed approach showed less bias than traditional STC for non-linear outcome models, and had lower mean squared error than MAIC, both under correct and incorrect specification of baseline covariate functional forms.
期刊介绍:
The Journal of Biopharmaceutical Statistics, a rapid publication journal, discusses quality applications of statistics in biopharmaceutical research and development. Now publishing six times per year, it includes expositions of statistical methodology with immediate applicability to biopharmaceutical research in the form of full-length and short manuscripts, review articles, selected/invited conference papers, short articles, and letters to the editor. Addressing timely and provocative topics important to the biostatistical profession, the journal covers:
Drug, device, and biological research and development;
Drug screening and drug design;
Assessment of pharmacological activity;
Pharmaceutical formulation and scale-up;
Preclinical safety assessment;
Bioavailability, bioequivalence, and pharmacokinetics;
Phase, I, II, and III clinical development including complex innovative designs;
Premarket approval assessment of clinical safety;
Postmarketing surveillance;
Big data and artificial intelligence and applications.