TY - JOUR
T1 - Comparison of numerical algorithms for bivariate sequential tests based on marginal criteria
AU - Zhao, Yanli
AU - Grambsch, Patricia M.
AU - Neaton, Jim
PY - 2005/6/1
Y1 - 2005/6/1
N2 - Group sequential tests are widely used for interim analyses in randomized clinical trials. These tests have been extended to bivariate outcomes, but calculation of boundary values is computationally intensive. In this paper, we compare 3 algorithms: (1) quasi-Monte Carlo; (2) Schervish's MULNOR; and (3) a bivariate version of Armitage's recursive formula proposed by Jennison and Turnbull, for calculating boundary values for the L-region bivariate design which takes account of the correlation between the outcomes. Up to 5 interim analyses (stages) and a range of values for the correlation between the two endpoints were considered. The three algorithms produced very similar boundary values, but the quasi-Monte Carlo approach was much faster than the other two. The quasi-Monte Carlo method is an attractive approach for studying higher dimensions - designs with more stages and designs with more than two outcomes. The increased speed of this algorithm may permit the development of more flexible monitoring guidelines for multiple endpoints for clinical trials.
AB - Group sequential tests are widely used for interim analyses in randomized clinical trials. These tests have been extended to bivariate outcomes, but calculation of boundary values is computationally intensive. In this paper, we compare 3 algorithms: (1) quasi-Monte Carlo; (2) Schervish's MULNOR; and (3) a bivariate version of Armitage's recursive formula proposed by Jennison and Turnbull, for calculating boundary values for the L-region bivariate design which takes account of the correlation between the outcomes. Up to 5 interim analyses (stages) and a range of values for the correlation between the two endpoints were considered. The three algorithms produced very similar boundary values, but the quasi-Monte Carlo approach was much faster than the other two. The quasi-Monte Carlo method is an attractive approach for studying higher dimensions - designs with more stages and designs with more than two outcomes. The increased speed of this algorithm may permit the development of more flexible monitoring guidelines for multiple endpoints for clinical trials.
KW - Bivariate responses
KW - Group sequential monitoring
KW - Numerical algorithms
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U2 - 10.1016/j.csda.2004.05.019
DO - 10.1016/j.csda.2004.05.019
M3 - Article
AN - SCOPUS:18744408121
SN - 0167-9473
VL - 49
SP - 631
EP - 641
JO - Computational Statistics and Data Analysis
JF - Computational Statistics and Data Analysis
IS - 3
ER -