Joint modeling of longitudinal endpoints and its applications to trial planning, monitoring and analysis.

IF 1.2 4区 医学 Q4 PHARMACOLOGY & PHARMACY
Liangcai Zhang, George Capuano, Vladimir Dragalin, John Jezorwski, Kim Hung Lo, Fei Chen
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Abstract

In the context of clinical trial practices, the study power and sample size are typically determined based on the expected treatment effects on the primary endpoint collected over time. The utilization of longitudinal modeling for the primary endpoint offers a flexible approach that has the potential to reduce the sample size and duration of the trial, thereby improving operational efficiency and costs. Joint modeling of multiple endpoints presents a unique opportunity to understand how the primary endpoint evolves over time with other clinically important endpoints, and has the potential to increase precision of estimates and therefore increase study power when designing a study at planning stage and enhance understanding and interpretation of the data at a multi-dimensional level at the analysis stage. This approach enables a comprehensive evaluation of clinical evidence from various perspectives, rather than relying solely on isolated pieces of information. Joint modeling of multiple longitudinal endpoints would also help trial monitoring process as the trial accumulates clinical evidence of efficacy data, and there is a high demand in developing tools for statistical learning the treatment benefits on the go especially when the endpoint(s) is not well-established yet in some therapeutic indications. In this article, we will illustrate the use of joint modeling of longitudinal endpoints and its applications to study design, analysis, and trial monitoring practices. Simulation studies suggest that the potential efficiency gain would be achieved via leveraging information within endpoint over time and/or between endpoints. We developed an R shiny application to aid in and support identifying promising efficacy signals from endpoints under investigation during the trial monitoring. The implementation of the joint models and the added values will be discussed through case studies and/or simulation studies.

纵向端点联合建模及其在试验计划、监测和分析中的应用。
在临床试验实践的背景下,研究能力和样本量通常是根据长期收集的主要终点的预期治疗效果来确定的。对主要终点的纵向建模提供了一种灵活的方法,有可能减少样本量和试验持续时间,从而提高操作效率和成本。多个终点的联合建模提供了一个独特的机会,可以了解主要终点如何随着时间的推移与其他临床重要终点一起演变,并且有可能提高估计的精度,从而在计划阶段设计研究时增加研究能力,并在分析阶段加强对多维水平数据的理解和解释。这种方法能够从不同的角度对临床证据进行综合评估,而不是仅仅依赖于孤立的信息。多个纵向终点的联合建模也将有助于试验监测过程,因为试验积累了疗效数据的临床证据,并且在开发用于统计学习治疗益处的工具方面有很高的需求,特别是在某些治疗适应症的终点尚未建立时。在本文中,我们将说明纵向端点的联合建模及其在研究设计、分析和试验监测实践中的应用。模拟研究表明,通过利用端点内的信息和/或端点之间的信息,可以获得潜在的效率增益。我们开发了一个R shiny应用程序,以帮助和支持在试验监测期间从调查的端点识别有希望的疗效信号。联合模型的实施和附加价值将通过案例研究和/或模拟研究进行讨论。
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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