代理端点评估的联邦数据分析方法。

IF 1.3 4区 医学 Q4 PHARMACOLOGY & PHARMACY
Dries De Witte, Ariel Alonso Abad, Diane Stephenson, Yashmin Karten, Antoine Leuzy, Gregory Klein, Geert Molenberghs
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引用次数: 0

摘要

在临床试验中,替代终点的成本效益更高,发生得更早,或者测量得更频繁,有时被用来取代昂贵的、迟到的或罕见的真正终点。监管机构通常需要彻底的评估和验证,以接受这些替代端点作为可靠的替代品。为此,元分析框架被认为是在试验和个体水平上验证代理人的一种非常可行的方法。然而,该框架需要来自多个试验或中心的数据,在数据共享不可行的情况下提出了挑战。在本文中,我们提出了一种联邦数据分析方法,该方法允许组织保持对其数据集的控制,同时仍然通过元分析技术启用代理验证。在这种方法中,不再需要原始数据共享。相反,在每个组织中进行独立分析。然后,将这些独立分析的结果汇总到一个中央分析中心,并提取代理评估的度量。我们将这种方法应用于模拟和真实的临床数据,展示了这种联合方法如何克服数据共享限制并验证分散设置中的代理端点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Federated Data Analysis Approach for the Evaluation of Surrogate Endpoints.

In clinical trials, surrogate endpoints, that are more cost-effective, occur earlier, or are more frequently measured, are sometimes used to replace costly, late, or rare true endpoints. Regulatory authorities typically require thorough evaluation and validation to accept these surrogate endpoints as reliable substitutes. To this end, the meta-analytic framework is considered a very viable approach to validate surrogates at both trial and individual levels. However, this framework requires data from multiple trials or centers, posing challenges when data sharing is not feasible. In this article, we propose a federated data analysis approach that allows organizations to maintain control over their datasets while still enabling surrogate validation through meta-analytic techniques. In this approach, there is no longer a need for raw data sharing. Instead, independent analyses are conducted at each organization. Thereafter, the results of these independent analyses are aggregated at a central analysis hub and the metrics for surrogate evaluation are extracted. We apply this approach to simulated and real clinical data, demonstrating how this federated approach can overcome data-sharing constraints and validate surrogate endpoints in decentralized settings.

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来源期刊
Pharmaceutical Statistics
Pharmaceutical Statistics 医学-统计学与概率论
CiteScore
2.70
自引率
6.70%
发文量
90
审稿时长
6-12 weeks
期刊介绍: Pharmaceutical Statistics is an industry-led initiative, tackling real problems in statistical applications. The Journal publishes papers that share experiences in the practical application of statistics within the pharmaceutical industry. It covers all aspects of pharmaceutical statistical applications from discovery, through pre-clinical development, clinical development, post-marketing surveillance, consumer health, production, epidemiology, and health economics. The Journal is both international and multidisciplinary. It includes high quality practical papers, case studies and review papers.
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