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缺失数据和未测量混杂因素对外部对照研究的影响分析:案例研究和模拟。

Examining the Effect of Missing Data and Unmeasured Confounding on External Comparator Studies: Case Studies and Simulations.

机构信息

IQVIA, Unterschweinstiege 2-14, 60549, Frankfurt, Germany.

European Medicines Agency, Domenico Scarlattilaan 6, Amsterdam, 1083 HS, The Netherlands.

出版信息

Drug Saf. 2024 Dec;47(12):1245-1263. doi: 10.1007/s40264-024-01467-9. Epub 2024 Aug 5.

Abstract

BACKGROUND AND OBJECTIVE

Missing data and unmeasured confounding are key challenges for external comparator studies. This work evaluates bias and other performance characteristics depending on missingness and unmeasured confounding by means of two case studies and simulations.

METHODS

Two case studies were constructed by taking the treatment arms from two randomised controlled trials and an external real-world data source that exhibited substantial missingness. The indications of the randomised controlled trials were multiple myeloma and metastatic hormone-sensitive prostate cancer. Overall survival was taken as the main endpoint. The effects of missing data and unmeasured confounding were assessed for the case studies by reporting estimated external comparator versus randomised controlled trial treatment effects. Based on the two case studies, simulations were performed broadening the settings by varying the underlying hazard ratio, the sample size, the sample size ratio between the experimental arm and the external comparator, the number of missing covariates and the percentage of missingness. Thereby, bias and other performance metrics could be quantified dependent on these factors.

RESULTS

For the multiple myeloma external comparator study, results were in line with the randomised controlled trial, despite missingness and potential unmeasured confounding, while for the metastatic hormone-sensitive prostate cancer case study missing data led to a low sample size, leading overall to inconclusive results. Furthermore, for the metastatic hormone-sensitive prostate cancer study, missing data in important eligibility criteria led to further limitations. Simulations were successfully applied to gain a quantitative understanding of the effects of missing data and unmeasured confounding.

CONCLUSIONS

This exploratory study confirmed external comparator strengths and limitations by quantifying the impact of missing data and unmeasured confounding using case studies and simulations. In particular, missing data in key eligibility criteria were seen to limit the ability to derive the external comparator target analysis population accurately, while simulations demonstrated the magnitude of bias to expect for various settings.

摘要

背景与目的

缺失数据和未测量的混杂是外部对照研究的关键挑战。本研究通过两个案例研究和模拟,评估了缺失数据和未测量混杂对偏倚和其他性能特征的影响。

方法

通过从两个随机对照试验和一个存在大量缺失数据的外部真实世界数据源中提取治疗组,构建了两个案例研究。随机对照试验的适应证为多发性骨髓瘤和转移性激素敏感前列腺癌。总生存期被作为主要终点。通过报告估计的外部对照与随机对照试验治疗效果,评估缺失数据和未测量混杂对案例研究的影响。基于这两个案例研究,通过改变潜在风险比、样本量、实验组与外部对照的样本量比、缺失协变量的数量和缺失率等参数,进行了模拟,从而可以量化这些因素对偏倚和其他性能指标的影响。

结果

对于多发性骨髓瘤外部对照研究,尽管存在缺失数据和潜在的未测量混杂,但结果与随机对照试验一致,而对于转移性激素敏感前列腺癌案例研究,缺失数据导致样本量较小,总体结果不确定。此外,对于转移性激素敏感前列腺癌研究,重要的入选标准缺失数据导致了进一步的限制。模拟成功地应用于定量理解缺失数据和未测量混杂的影响。

结论

本探索性研究通过使用案例研究和模拟量化缺失数据和未测量混杂的影响,证实了外部对照的优势和局限性。特别是,关键入选标准中的缺失数据被认为限制了准确得出外部对照目标分析人群的能力,而模拟则演示了在各种情况下预期的偏倚幅度。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dae1/11554740/fcf7859c7d3d/40264_2024_1467_Fig1_HTML.jpg

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