Simulated treatment comparisons with jackknife pseudo values for estimating population-adjusted marginal treatment effects.

IF 1.3 4区 医学 Q4 PHARMACOLOGY & PHARMACY
Sean Yiu, Kirsty Rhodes
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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.

模拟处理比较与小刀伪值估计人口调整后的边际处理效果。
匹配调整间接比较(MAIC)和模拟治疗比较(STC)通常用于间接治疗比较,当患者水平的数据可用于某些治疗而不能用于其他治疗时。然而,当试验之间的协变量重叠有限时,MAIC可能会变得低效,并且当使用非线性结果模型(如logistic或生存模型)时,STC可能无法估计卫生技术评估所需的边际(人口平均)治疗效果。我们提出了一种新的STC方法来解决这些限制。对于可以假设治疗效果的线性模型的设置(例如对数优势比或对数风险比),我们建议使用STC与边际治疗效果估计的折刀伪值作为因变量,而不是观察结果。这些伪值将边际治疗效果估计分解为个体患者贡献,然后可以根据患者水平特征进行回归,以预测替代目标人群的边际治疗效果。我们使用两个涉及非线性结果模型的工作示例来说明该方法。在对连续、二元和事件时间结果的模拟试验中,无论在基线协变量函数形式的正确和错误规范下,该方法在非线性结果模型上的偏倚都小于传统的STC,均方误差都低于MAIC。
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来源期刊
Journal of Biopharmaceutical Statistics
Journal of Biopharmaceutical Statistics 医学-统计学与概率论
CiteScore
2.50
自引率
18.20%
发文量
71
审稿时长
6-12 weeks
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.
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