Thall Peter F
Department of Biostatistics, University of Texas, M.D. Anderson Cancer Center, 1515 Holcombe Boulevard, Houston, TX 77030, USA.
Lifetime Data Anal. 2008 Mar;14(1):37-53. doi: 10.1007/s10985-007-9049-x. Epub 2007 Sep 2.
This article reviews phase 2-3 clinical trial designs, including their genesis and the potential role of such designs in treatment evaluation. The paper begins with a discussion of the many scientific flaws in the conventional phase 2 --> phase 3 treatment evaluation process that motivate phase 2-3 designs. This is followed by descriptions of some particular phase 2-3 designs that have been proposed, including two-stage designs to evaluate one experimental treatment, a design that accommodates both frontline and salvage therapy in oncology, two-stage select-and-test designs that evaluate several experimental treatments, dose-ranging designs, and a seamless phase 2-3 design based on both early response-toxicity outcomes and later event times. A general conclusion is that, in many circumstances, a properly designed phase 2-3 trial utilizes resources much more efficiently and provides much more reliable inferences than conventional methods.
本文回顾了2期至3期临床试验设计,包括其起源以及此类设计在治疗评估中的潜在作用。本文首先讨论了传统的2期至3期治疗评估过程中存在的许多科学缺陷,这些缺陷促使了2期至3期设计的产生。接下来描述了一些已提出的特定2期至3期设计,包括评估一种实验性治疗的两阶段设计、一种适用于肿瘤学一线和挽救治疗的设计、评估几种实验性治疗的两阶段选择和测试设计、剂量范围设计以及基于早期反应毒性结果和后期事件时间的无缝2期至3期设计。一个总体结论是,在许多情况下,精心设计的2期至3期试验比传统方法更有效地利用资源,并提供更可靠的推断。