Comparison of four sequential methods allowing for early stopping of comparative clinical trials

被引:19
作者
Sebille, V [1 ]
Bellissant, E [1 ]
机构
[1] Fac Med, Lab Pharmacol Expt & Clin, F-35043 Rennes, France
关键词
group sequential tests; one-parameter boundaries; sequential probability ratio test; simulation study; triangular test;
D O I
10.1042/CS19990336
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Phase III trials aim to assess whether a new treatment has superior efficacy than a standard treatment. Sequential methods, such as the sequential probability ratio test (SPRT), the triangular test (TT) and so-called one-parameter boundaries (OPB), now allow early stopping of such trials, both in the case of efficacy (alternative hypothesis; H-1) and in the case of lack of efficacy (null hypothesis; H-0). We compared the statistical properties of the SPRT and the TT, and of OPE with Pocock (OPBDelta-0.5) and O'Brien and Fleming (OPBDelta-0) type boundaries, in the setting of one-sided comparative trials with normal response. We studied the type I error (alpha), power (1-beta), average sample number (ASN) and 90th percentile (P90) of the number of patients required to reach a conclusion using simulations. The four tests were also compared with the corresponding single-stage design (SSD). All sequential tests display alpha and 1-beta close to nominal values and, as compared with SSD, allow important decreases in ASN: for example, -48%, -42%, -40% and -31% under H-0 and H-1 for SPRT, TT, OPBDelta-0.5 and OPBDelta-0 respectively. For situations between H-0 and H-1, ASNs of all sequential tests were still smaller than the sample size required by SSD, with the TT displaying the largest decrease (-25%). The P90s of the TT and OPBDelta-0 under H-0 and H-1 were smaller than the P90s of the SPRT and OPBDelta-0.5, which were similar to the sample size required by SSD. If all sequential tests display approximately similar features, the TT is the most appealing regarding decreases in sample size, especially for situations between H-0 and H-1.
引用
收藏
页码:569 / 578
页数:10
相关论文
共 38 条
[21]  
LIN DY, 1991, BIOMETRIKA, V78, P123
[22]   MULTIPLE TESTING PROCEDURE FOR CLINICAL-TRIALS [J].
OBRIEN, PC ;
FLEMING, TR .
BIOMETRICS, 1979, 35 (03) :549-556
[23]   GROUP SEQUENTIAL DESIGNS FOR ONE-SIDED AND 2-SIDED HYPOTHESIS-TESTING WITH PROVISION FOR EARLY STOPPING IN FAVOR OF THE NULL HYPOTHESIS [J].
PAMPALLONA, S ;
TSIATIS, AA .
JOURNAL OF STATISTICAL PLANNING AND INFERENCE, 1994, 42 (1-2) :19-35
[24]   THE CHART TRIALS - BAYESIAN DESIGN AND MONITORING IN PRACTICE [J].
PARMAR, MKB ;
SPIEGELHALTER, DJ ;
FREEDMAN, LS .
STATISTICS IN MEDICINE, 1994, 13 (13-14) :1297-1312
[25]   GROUP SEQUENTIAL METHODS IN DESIGN AND ANALYSIS OF CLINICAL-TRIALS [J].
POCOCK, SJ .
BIOMETRIKA, 1977, 64 (02) :191-200
[26]   A BAYESIAN GROUP SEQUENTIAL DESIGN FOR A MULTIPLE ARM RANDOMIZED CLINICAL-TRIAL [J].
ROSNER, GL ;
BERRY, DA .
STATISTICS IN MEDICINE, 1995, 14 (04) :381-394
[27]  
Siegmund D., 1985, SEQUENTIAL ANAL TEST
[28]   BAYESIAN APPROACHES TO RANDOMIZED TRIALS [J].
SPIEGELHALTER, DJ ;
FREEDMAN, LS ;
PARMAR, MKB .
JOURNAL OF THE ROYAL STATISTICAL SOCIETY SERIES A-STATISTICS IN SOCIETY, 1994, 157 :357-387
[29]   ON THE DESIGN AND ANALYSIS OF RANDOMIZED CLINICAL-TRIALS WITH MULTIPLE END-POINTS [J].
TANG, DI ;
GELLER, NL ;
POCOCK, SJ .
BIOMETRICS, 1993, 49 (01) :23-30
[30]   DESIGN OF GROUP SEQUENTIAL CLINICAL-TRIALS WITH MULTIPLE ENDPOINTS [J].
TANG, DI ;
GNECCO, C ;
GELLER, NL .
JOURNAL OF THE AMERICAN STATISTICAL ASSOCIATION, 1989, 84 (407) :776-779