Thall P F, Simon R, Ellenberg S S
Statistics/Computer & Information Systems Department, George Washington University, Washington, D.C. 20052.
Biometrics. 1989 Jun;45(2):537-47.
In clinical trials where several experimental treatments are of interest, the goal may be viewed as identification of the best of these and comparison of that treatment to a standard control therapy. However, it is undesirable to commit patients to a large-scale comparative trial of a new regimen without evidence that its therapeutic success rate is acceptably high. We propose a two-stage design in which patients are first randomized among the experimental treatments, and the single treatment having the highest observed success rate is identified. If this highest rate falls below a fixed cutoff then the trial is terminated. Otherwise, the "best" new treatment is compared to the control at a second stage. Locally optimal values of the cutoff and the stage-1 and stage-2 sample sizes are derived by minimizing expected total sample size. The design has both high power and high probability of terminating early when no experimental treatment is superior to the control. Numerical results for implementing the design are presented, and comparison to Dunnett's (1984, in Design of Experiments: Ranking and Selection, T. J. Santner and A. C. Tamhane (eds), 47-66; New York: Marcel Dekker) optimal one-stage procedure is made.
在有几种实验性治疗方法值得关注的临床试验中,目标可以被视为确定其中最佳的治疗方法,并将该治疗方法与标准对照疗法进行比较。然而,在没有证据表明新方案的治疗成功率足够高的情况下,让患者参与新方案的大规模对比试验是不可取的。我们提出一种两阶段设计,首先将患者随机分配到各种实验性治疗方法中,确定观察到的成功率最高的单一治疗方法。如果这个最高率低于一个固定的临界值,那么试验就终止。否则,在第二阶段将“最佳”新治疗方法与对照进行比较。通过最小化预期总样本量来得出临界值以及第一阶段和第二阶段样本量的局部最优值。该设计在没有实验性治疗方法优于对照时,具有高功效和高概率提前终止试验的特点。给出了实施该设计的数值结果,并与邓尼特(1984年,《实验设计:排序与选择》,T. J. 桑特纳和A. C. 塔姆哈尼(编),第47 - 66页;纽约:马塞尔·德克尔)的最优单阶段程序进行了比较。