Chen T T
Biometric Research Branch, National Cancer Institute, Bethesda, Maryland 20892, USA.
Stat Med. 1997 Dec 15;16(23):2701-11. doi: 10.1002/(sici)1097-0258(19971215)16:23<2701::aid-sim704>3.0.co;2-1.
The objective of a phase II cancer clinical trial is to screen a treatment that can produce a similar or better response rate compared to the current treatment results. This screening is usually carried out in two stages as proposed by Simon. For ineffective treatment, the trial should terminate at the first stage. Ensign et al. extended two-stage optimal designs to three stages; however, they restricted the rejection region in the first stage to be zero response, and the sample size to at least 5. This paper extends Simon's two-stage to a three-stage design without these restrictions, and provides tables for both optimal and minimax designs. One can use the three-stage design to reduce the expected sample size when the treatment is not promising a priori and when the accrual rate is slow. The average reduction in size from a two-stage to three-stage design is 10 per cent.
II期癌症临床试验的目的是筛选出一种与当前治疗结果相比能产生相似或更好缓解率的治疗方法。这种筛选通常按照西蒙提出的分两个阶段进行。对于无效治疗,试验应在第一阶段终止。恩赛因等人将两阶段最优设计扩展到了三阶段;然而,他们将第一阶段的拒绝区域限制为零缓解,且样本量至少为5。本文将西蒙的两阶段设计扩展为无这些限制的三阶段设计,并提供了最优设计和极小极大设计的表格。当治疗在一开始就没有前景且入组率缓慢时,可以使用三阶段设计来减少预期样本量。从两阶段设计到三阶段设计,样本量平均减少10%。