Analysis of Failure Time Data Arising From Studies With Alternating Treatment Schedules
交替治疗安排研究中的失效时间数据分析AI 解读 ↓
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。
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。
AI 根据所提供的论文材料归类:摘要明确以交替治疗资料推断持续治疗下的事件分布,涉及治疗方案反事实的推断。
交替治疗安排研究中的失效时间数据分析AI 解读 ↓
正在核对关联版本…
正在核对对应版本的资源…
We develop statistical methods for designing and analyzing studies in which treatments are deliberately interrupted and reinitiated, but where interest lies in making inferences about continuous treatment use. We refer to such designs as alternating designs, because subjects alternate between periods in which they are taking the treatment of interest and periods when they are not. Our goals are to determine how to estimate the distribution of time to an event if the treatment were given continuously, to compare the distributions of two such continuously given treatments, and to assess the effects of covariates on the distribution of a continuously given treatment. We examine a nonparametric estimator of the cumulative hazard function for continuous treatment using data from an alternating design and show it to be uniformly consistent and asymptotically normal under certain conditions relating to the effects of interrupting the treatment. We then introduce nonparametric tests for comparing the distributions corresponding to two such continuously given treatments and derive their asymptotic properties under general alternatives to the null and under various conditions related to the interruption of treatment. We compare the properties of the alternating treatment design and the classical parallel group design and present results from a simulation study that assesses the size and power of the test procedures introduced. Finally, we examine partial likelihood methods for assessing the effects of covariates and continuous treatment on time until an event under a proportional hazards model. We illustrate the proposed methods using the results from a recent study in which subjects alternate between taking an active drug and placebo on an annual basis.