Missing data in the eligibility criteria of synthetic controls from real-world data.

IF 1.2 4区 医学 Q4 PHARMACOLOGY & PHARMACY
Liang Li, Thomas Jemielita, Cong Chen
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引用次数: 0

Abstract

Randomized clinical trials (RCTs) can benefit from using Real-World Data (RWD) as a supplementary data source to enhance their analysis. An Augmented RCT combines randomized treatment and control groups with synthetic controls derived from RWD. This way, the trial can achieve less prospective enrollment, higher statistical power, and lower costs. However, to ensure scientific validity, the synthetic controls must satisfy the same eligibility criteria as the trial participants. A major challenge is that RWD often have missing data that hinder the eligibility assessment. This problem has been overlooked in the literature and this paper offers statistical solutions to address it. We use multiple imputations to handle missing data in the variables involved in the eligibility criteria. We also propose a generalized propensity score weighting procedure to adjust for the life expectancy requirement, a common eligibility criterion in oncology clinical trials but usually unavailable in RWD. Since the life expectancy is an unmeasured confounder, we discuss the statistical assumptions required to correct its bias. We validate the proposed solutions through simulation studies and the analysis of an Augmented RCT in oncology.

真实世界数据合成控制的合格标准中缺少数据。
随机临床试验(rct)可以受益于使用真实世界数据(RWD)作为补充数据源,以加强其分析。增强型随机对照试验将随机治疗和对照组与RWD衍生的合成对照组相结合。通过这种方式,试验可以实现更少的预期入组,更高的统计能力和更低的成本。然而,为了确保科学有效性,合成对照必须满足与试验参与者相同的资格标准。一个主要的挑战是RWD经常缺少数据,这阻碍了资格评估。这个问题在文献中被忽视了,本文提供了统计解决方案来解决这个问题。我们使用多个imputations来处理缺失的数据在变量中涉及的资格标准。我们还提出了一个广义倾向评分加权程序来调整预期寿命要求,这是肿瘤临床试验中常见的资格标准,但通常不适用于RWD。由于预期寿命是一个无法测量的混杂因素,我们讨论纠正其偏差所需的统计假设。我们通过模拟研究和肿瘤学增强RCT分析验证了提出的解决方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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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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