非比例风险下的双样本推理程序。

IF 1.3 4区 医学 Q4 PHARMACOLOGY & PHARMACY Pharmaceutical Statistics Pub Date : 2023-11-01 Epub Date: 2023-07-10 DOI:10.1002/pst.2324
Yi-Cheng Tai, Weijing Wang, Martin T Wells
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引用次数: 0

摘要

我们引入了一个新的双样本推理程序来评估两组随时间的相对表现。我们的无模型方法没有假设成比例的风险,使其适用于可能存在非比例风险的情况。我们的程序包括一个诊断tau图来识别危险时间的变化和一个正式的推理程序。我们开发的基于tau的测量具有临床意义,并提供可解释的估计,以总结随时间推移的治疗效果。我们提出的统计量是u统计量,并显示鞅结构,允许我们构建置信区间并执行假设检验。我们的方法对于审查分布是稳健的。我们还演示了如何将我们的方法应用于由于跟踪不足而导致尾部信息缺失的情况下的敏感性分析。在不进行删节的情况下,我们提出的Kendall的tau估计量可以简化为Wilcoxon-Mann-Whitney统计量。我们使用模拟来评估我们的方法,将其性能与受限的平均生存时间和log-rank统计进行比较。我们还将我们的方法应用于一些已发表的肿瘤学临床试验的数据,其中可能存在非比例风险。
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Two-sample inference procedures under nonproportional hazards.

We introduce a new two-sample inference procedure to assess the relative performance of two groups over time. Our model-free method does not assume proportional hazards, making it suitable for scenarios where nonproportional hazards may exist. Our procedure includes a diagnostic tau plot to identify changes in hazard timing and a formal inference procedure. The tau-based measures we develop are clinically meaningful and provide interpretable estimands to summarize the treatment effect over time. Our proposed statistic is a U-statistic and exhibits a martingale structure, allowing us to construct confidence intervals and perform hypothesis testing. Our approach is robust with respect to the censoring distribution. We also demonstrate how our method can be applied for sensitivity analysis in scenarios with missing tail information due to insufficient follow-up. Without censoring, Kendall's tau estimator we propose reduces to the Wilcoxon-Mann-Whitney statistic. We evaluate our method using simulations to compare its performance with the restricted mean survival time and log-rank statistics. We also apply our approach to data from several published oncology clinical trials where nonproportional hazards may exist.

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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.
期刊最新文献
Optimizing Sample Size Determinations for Phase 3 Clinical Trials in Type 2 Diabetes. Prediction Intervals for Overdispersed Poisson Data and Their Application in Medical and Pre-Clinical Quality Control. Treatment Effect Measures Under Nonproportional Hazards. Bayesian Response Adaptive Randomization for Randomized Clinical Trials With Continuous Outcomes: The Role of Covariate Adjustment. PKBOIN-12: A Bayesian Optimal Interval Phase I/II Design Incorporating Pharmacokinetics Outcomes to Find the Optimal Biological Dose.
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