Design Issues in Randomized Phase II/III Trials

被引:47
作者
Korn, Edward L. [1 ]
Freidlin, Boris
Abrams, Jeffrey S.
Halabi, Susan [2 ]
机构
[1] NCI, Biometr Res Branch, Bethesda, MD 20852 USA
[2] Duke Univ, Med Ctr, Durham, NC USA
关键词
CLINICAL-TRIALS; INTERIM; AGENTS; SELECTION;
D O I
10.1200/JCO.2011.38.5732
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Phase II trials are used to show sufficient preliminary activity of a new treatment (in single-arm designs or randomized screening designs) or to select among treatments with demonstrated activity (in randomized selection designs). The treatments prioritized in a phase II trial are then tested definitively against a control treatment in a randomized phase III trial. Randomized phase II/III trials use an adaptive trial design that combines these two types of trials in one, with potential gains in time and reduced numbers of patients required to be treated. Two key considerations in designing a phase II/III trial are whether to suspend accrual while the phase II data mature and the choice of phase II target treatment effect. We discuss these phase II/III design parameters, give examples of phase II/III trials, and provide recommendations concerning efficient phase II/III trial designs. J Clin Oncol 30: 667-671. (C) 2012 by American Society of Clinical Oncology
引用
收藏
页码:667 / 671
页数:5
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