Randomization, balance, and the validity and efficiency of design-adaptive allocation methods

被引:48
作者
Aickin, M [1 ]
机构
[1] Ctr Hlth Res, Portland, OR 97227 USA
关键词
clinical trials; imbalance minimization; minimum likelihood allocation; simulation; logistic regression; complete randomization;
D O I
10.1016/S0378-3758(00)00228-7
中图分类号
O21 [概率论与数理统计]; C8 [统计学];
学科分类号
020208 ; 070103 ; 0714 ;
摘要
Few topics have stirred as much discussion and controversy as randomization. A reading of the literature suggests that clinical trialists generally feel randomization is necessary for valid inference, while biostatisticians using model-based inference often appear to prefer nearly optimal designs irrespective of any induced randomness. Dissection of the methods of treatment assignment shows that there are five basic approaches; pure randomizers, true randomizers, quasi-randomizers, permutation testers, and conventional modelers. Four of these have coherent design and analysis strategies, even though they are not mutually consistent, but the fifth and most prevalent approach (quasi-randomization) has little to recommend it. Design-adaptive allocation is defined, it is shown to provide valid inference, and a simulation indicates its efficiency advantage. In small studies, or large studies with many important prognostic covariates or analytic subgroups, design-adaptive allocation is an extremely attractive method of treatment assignment. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:97 / 119
页数:23
相关论文
共 25 条
[2]   A PROGRAM FOR BALANCING THE ALLOCATION OF SUBJECTS TO TREATMENT IN A CLINICAL-TRIAL [J].
AICKIN, M .
COMPUTERS AND BIOMEDICAL RESEARCH, 1982, 15 (06) :519-524
[3]  
[Anonymous], LATENT VARIABLE MODE
[4]   TREATMENT ALLOCATION PROCEDURE FOR SEQUENTIAL CLINICAL-TRIALS [J].
BEGG, CB ;
IGLEWICZ, B .
BIOMETRICS, 1980, 36 (01) :81-90
[5]   SIGNIFICANCE TESTS OF COVARIATE IMBALANCE IN CLINICAL-TRIALS [J].
BEGG, CB .
CONTROLLED CLINICAL TRIALS, 1990, 11 (04) :223-225
[6]   ADAPTIVE ALLOCATION IN RANDOMIZED CONTROLLED TRIALS [J].
BIRKETT, NJ .
CONTROLLED CLINICAL TRIALS, 1985, 6 (02) :146-155
[7]  
EFRON B, 1971, BIOMETRIKA, V58, P403, DOI 10.2307/2334377
[8]  
FEINSTEIN AR, 1975, J CHRON DIS, V29, P277
[9]  
Forsythe AB, 1977, 28 U CAL HLTH SCI CO
[10]  
Good P, 1993, PERMUTATION TESTS