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Noninferiority trial designs for odds ratios and risk differences
被引:15
|作者:
Hilton, Joan F.
[1
]
机构:
[1] Univ Calif San Francisco, Dept Epidemiol & Biostat, San Francisco, CA 94107 USA
关键词:
active-controlled trial;
allocation ratio;
ancillary parameter;
SAMPLE-SIZE FORMULAS;
STANDARD THERAPY;
ELUTING STENTS;
ENDARTERECTOMY;
CAPECITABINE;
LAMIVUDINE;
VACCINE;
SAFETY;
MARGIN;
TESTS;
D O I:
10.1002/sim.3846
中图分类号:
Q [生物科学];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
This study presents constrained maximum likelihood derivations of the design parameters of noninferiority trials for binary outcomes with the margin defined on the odds ratio (psi) or risk-difference (delta) scale. The derivations show that, for trials in which the group-specific response rates are equal under the point-alternative hypothesis, the common response rate, pi(N), is a fixed design parameter whose value lies between the control and experimental rates hypothesized at the point-null, {pi(C),pi(E)}. We show that setting pi(N) equal to the value of pi(C) that holds under H-0 underestimates the overall sample size requirement. Given {pi(C),psi} or {pi(C),delta} and the type I and II error rates, or algorithm finds clinically meaningful design values of pi(N), and the corresponding minimum asymptotic sample size, N = n(E) + n(C), and optimal allocation ratio, gamma = n(E)/n(C). We find that optimal allocations are increasingly imbalanced as psi increases, with gamma(psi) < 1 and gamma(delta) approximate to 1/gamma(psi), and that ranges of allocation ratios map to the minimum sample size. The latter characteristic allows trialists to consider trade-offs between optimal allocation at a smaller N and a preferred allocation at a larger N. For designs with relatively large margins (e.g. psi > 2.5), trial results that are presented on both scales will differ in power, with more power lost if the study is designed on the risk-difference scale and reported on the odds ratio scale than vice versa. Copyright (C) 2010 John Wiley & Sons, Ltd.
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页码:982 / 993
页数:12
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