跳到正文
← 返回论文列表与筛选
阅读说明

本页整理公开书目信息,不生成学术质量评分。AI 解读根据题名及所注明的摘要或原文片段生成,未完成全文核验,可能有误;具体假设、证明与结论请核对原文。摘要保留来源文本,未经模型改写。

DOI 首次登记不等于接收或发表日期。部分更正、评论等条目没有独立摘要;缺少可靠材料时保留待补状态。

本页为预印本版本;arXiv 收录、作者填写的期刊信息以及作者既有发表经历,都不单独证明本篇已接收。作者发表记录按 OpenAlex 身份与完整姓名、本站覆盖期刊 ISSN 及正式卷期核对,只展示已核实例,档案仍可能误合并。

引用量采用 OpenAlex 单条关联记录,不合计多个记录;关联记录可能包含正式发表版本,不等于此版本单独引用。缺失不视为零,引用指标不代表论文质量。

关注作者按书目中的完整姓名匹配,同名和姓名变体需人工辨别。相关论文先按共享细分方向和具体方法排列,再参考通用方法与发表日期。

分类依据与纠错

AI 根据所提供的论文材料归类:摘要研究临床治疗效应,并以中位数和整体现实结局分布的概率比较刻画分布异质性。

反馈分类问题

正在核对关联版本…

代码、数据与补充材料

正在核对对应版本的资源…

关注这篇论文的作者
Kazushi Maruo
Ryota Ishii
Yusuke Yamaguchi
Toshio Shimokawa
Tomoyuki Sugimoto
Masahiko Gosho

偏态结局纵向临床研究中的灵活治疗效应推断框架

研究问题
当临床纵向结局的偏度和分布形状随治疗组与时间变化时,如何避免共同变换参数带来的偏差,并描述超出中位数的效应?
方法与思路
作者提出 Box–Cox 多变量回归,允许变换参数按组和时间变化,推断中位数差及一组随机患者结局优于另一组的概率。
材料陈述的贡献
摘要称,模拟中该框架在分布形状不同的情形下提供近乎无偏估计,概率型效应指标在稳健性与统计效率间取得有利平衡。
阅读关注点
应核对变换与纵向相关结构的设定、缺失数据处理、概率型效应的精确定义,以及治疗效应解释所依赖的研究设计。
阅读边界
这是 arXiv 预印本,不能据此认定已同行评审或期刊接收;摘要未说明完整模型及缺失机制,模拟结论不能推广至所有偏态分布。

原文摘要

Longitudinal continuous outcomes in clinical trials are commonly analyzed using mixed models for repeated measures (MMRM) under normality assumptions. However, many clinical outcomes are skewed, making mean-based treatment effects difficult to interpret and potentially reducing statistical efficiency. The Box--Cox MMRM (BCMMRM) approach accommodates skewness by enabling inference on model-based median differences via inverse transformation. However, BCMMRM typically assumes a common transformation parameter across treatment groups and time points. When distributional shapes differ between groups or evolve over time, this assumption may lead to biased treatment effect. Furthermore, when treatment affects not only central tendency but also distributional shape or tail behavior, treatment effects may not be adequately characterized by a single location summary such as the median. We propose the Box--Cox multivariate regression (BCMVR) framework for longitudinal data with skewed outcomes. BCMVR relaxes this restriction by allowing transformation parameters to vary across groups and time points. The framework enables inference based on interpretable summaries, including median differences and a probability-based treatment effect quantifying the probability that a randomly selected patient in one group has a better outcome than one in another group. This measure integrates information over the entire outcome distribution and provides a complementary summary when distributional shapes differ. Simulation studies demonstrate that BCMMRM can produce biased estimates when distributions differ in shape, whereas BCMVR provides nearly unbiased estimation. The probability-based measure achieves a favorable balance between robustness and statistical efficiency. The proposed framework provides a flexible and interpretable approach to treatment effect inference under distributional heterogeneity.

笔记与分组
相关领域论文