Kim K
Department of Biostatistics, Harvard School of Public Health, Boston, Massachusetts.
Stat Med. 1992 Aug;11(11):1477-88. doi: 10.1002/sim.4780111106.
The study duration in a clinical trial with censored survival data is the sum of the accrual duration, which determines the sample size in a traditional sense, and the follow-up duration, which more or less controls the number of events to be observed. We propose a design procedure for determining the study duration or for calculating the power in a group sequential clinical trial with censored survival data and possibly unequal patient allocation between treatments, adjusting for stratified randomization. The group sequential method is based on the use function approach. We describe a clinical trial recently activated by the Eastern Cooperative Oncology Group for an illustration of the proposed procedure.
在具有删失生存数据的临床试验中,研究持续时间是累积持续时间与随访持续时间之和,累积持续时间从传统意义上决定样本量,随访持续时间或多或少控制要观察的事件数量。我们提出一种设计程序,用于确定具有删失生存数据且各治疗组间患者分配可能不等的成组序贯临床试验中的研究持续时间或计算检验效能,并针对分层随机化进行调整。成组序贯方法基于使用函数法。我们描述了东部肿瘤协作组最近启动的一项临床试验,以说明所提出的程序。