临床试验中时间到事件安全终点的顺序监测。

IF 2.2 3区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
Clinical Trials Pub Date : 2025-06-01 Epub Date: 2024-12-29 DOI:10.1177/17407745241304119
Michael J Martens, Qinghua Lian, Nancy L Geller, Eric S Leifer, Brent R Logan
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引用次数: 0

摘要

背景/目的安全监测是II期和III期临床试验的关键要求。为了保护患者免受毒性风险,可能会实施停止规则,如果意外发生大量事件,将停止研究。这些规则是使用统计程序构建的,这些程序通常将毒性数据视为二元事件。由于毒性的确切日期通常是可用的,因此将这些数据作为事件时间数据处理的策略可能会提供更高的能力,并且需要更少的日历时间来识别超额风险。这项工作研究了几种用于监控安全事件的统计方法,并说明了我们设计和评估这些程序的R软件包。方法通过Wang-Tsiatis检验、贝叶斯伽玛泊松模型和序贯概率比检验得出的安全停车规则的性能指标,在II期和III期试验情景下进行评价和对比。我们开发了一个公开可用的R包“停止规则”,用于设计和评估这些停止规则,其效用通过血液和骨髓移植临床试验网络1204(国家临床试验编号NCT01998633)的停止规则的设计来说明,这是一项多中心,II期,单臂试验,评估骨髓移植治疗噬血细胞淋巴组织细胞病和原发性免疫缺陷的有效性和安全性。结果如先前在组序贯试验设置中所见,在研究早期具有严格停止标准的规则往往在试验后期具有更宽松的停止标准。因此,积极的早期监测方法,如具有弱先验的伽马-泊松模型和某些截断顺序概率比测试的选择,通常比在早期阶段更允许的方法产生更少的毒性和更低的功率,如具有强先验的伽马-泊松模型和O'Brien-Fleming测试。然而,Pocock试验和最大化序列概率比试验的结果与这些趋势相反,由于其极端激进的早期停止标准,与其他方法相比,显示出功率降低和毒性数量增加,未能保留足够的功率来识别研究开始后的安全问题。与二元毒性方法相比,我们的时间-事件方法在考虑的各种情况下可将预期毒性降低20%。结论安全监测程序旨在保护研究参与者免受不安全治疗的暴露和毒性。为此,我们建议考虑以时间-事件为导向的伽马-泊松模型-弱先验模型或截断序列概率比检验来构建安全停车规则,因为在我们的研究中,它们在最小化毒性数量方面表现最好。我们的R包“停止规则”提供了创建和评估停止规则的程序,以帮助试验设计。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Sequential monitoring of time-to-event safety endpoints in clinical trials.

Background/aimsSafety monitoring is a crucial requirement for Phase II and III clinical trials. To protect patients from toxicity risk, stopping rules may be implemented that will halt the study if an unexpectedly high number of events occur. These rules are constructed using statistical procedures that typically treat the toxicity data as binary occurrences. Because the exact dates of toxicities are often available, a strategy that handles these as time-to-event data may offer higher power and require less calendar time to identify excess risk. This work investigates several statistical methods for monitoring safety events as time-to-event endpoints and illustrates our R software package for designing and evaluating these procedures.MethodsThe performance metrics of safety stopping rules derived from Wang-Tsiatis tests, Bayesian Gamma-Poisson models, and sequential probability ratio tests are evaluated and contrasted in Phase II and III trial scenarios. We developed a publicly available R package "stoppingrule" for designing and assessing these stopping rules whose utility is illustrated through the design of a stopping rule for Blood and Marrow Transplant Clinical Trials Network 1204 (National Clinical Trial number NCT01998633), a multicenter, Phase II, single-arm trial that assessed the efficacy and safety of bone marrow transplant for the treatment of hemophagocytic lymphohistiocytosis and primary immune deficiencies.ResultsAs seen previously in group sequential testing settings, rules with strict stopping criteria early in a study tend to have more lenient stopping criteria late in the trial. Consequently, methods with aggressive early monitoring, such as Gamma-Poisson models with weak priors and certain choices of truncated sequential probability ratio tests, usually yield a smaller number of toxicities and lower power than ones that are more permissive at early stages, such as Gamma-Poisson models with strong priors and the O'Brien-Fleming test. The Pocock test and maximized sequential probability ratio test performed contrary to these trends, however, exhibiting both diminished power and higher numbers of toxicities than other methods due to their extremely aggressive early stopping criteria, failing to reserve adequate power to identify safety issues beyond the start of the study. In contrast to binary toxicity approaches, our time-to-event methods offer meaningful reductions in expected toxicities of up to 20% across scenarios considered.ConclusionSafety monitoring procedures aim to guard study participants from being exposed to and suffering toxicity from unsafe treatments. Toward this end, we recommend considering the time-to-event-oriented Gamma-Poisson model-weak prior model or truncated sequential probability ratio test for constructing safety stopping rules, as they performed the best in minimizing the number of toxicities in our investigations. Our R package "stoppingrule" offers procedures for creating and assessing stopping rules to aid trial design.

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来源期刊
Clinical Trials
Clinical Trials 医学-医学:研究与实验
CiteScore
4.10
自引率
3.70%
发文量
82
审稿时长
6-12 weeks
期刊介绍: Clinical Trials is dedicated to advancing knowledge on the design and conduct of clinical trials related research methodologies. Covering the design, conduct, analysis, synthesis and evaluation of key methodologies, the journal remains on the cusp of the latest topics, including ethics, regulation and policy impact.
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