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序贯样本量重新估计试验后参数估计及其精确置信区间

Estimation of a parameter and its exact confidence interval following sequential sample size reestimation trials.

作者信息

Cheng Yi, Shen Yu

机构信息

Department of Mathematical Sciences, Indiana University at South Bend, South Bend, Indiana 46634, USA.

出版信息

Biometrics. 2004 Dec;60(4):910-8. doi: 10.1111/j.0006-341X.2004.00246.x.

Abstract

For confirmatory trials of regulatory decision making, it is important that adaptive designs under consideration provide inference with the correct nominal level, as well as unbiased estimates, and confidence intervals for the treatment comparisons in the actual trials. However, naive point estimate and its confidence interval are often biased in adaptive sequential designs. We develop a new procedure for estimation following a test from a sample size reestimation design. The method for obtaining an exact confidence interval and point estimate is based on a general distribution property of a pivot function of the Self-designing group sequential clinical trial by Shen and Fisher (1999, Biometrics55, 190-197). A modified estimate is proposed to explicitly account for futility stopping boundary with reduced bias when block sizes are small. The proposed estimates are shown to be consistent. The computation of the estimates is straightforward. We also provide a modified weight function to improve the power of the test. Extensive simulation studies show that the exact confidence intervals have accurate nominal probability of coverage, and the proposed point estimates are nearly unbiased with practical sample sizes.

摘要

对于用于监管决策的验证性试验,重要的是所考虑的适应性设计要能在实际试验中为治疗比较提供具有正确名义水平的推断、无偏估计以及置信区间。然而,在适应性序贯设计中,简单的点估计及其置信区间往往存在偏差。我们针对样本量重新估计设计中的检验开发了一种新的估计程序。获得精确置信区间和点估计的方法基于Shen和Fisher(1999年,《生物统计学》55卷,190 - 197页)的自设计组序贯临床试验枢轴函数的一般分布特性。当块大小时,提出了一种修正估计,以明确考虑无效性停止边界并减少偏差。所提出的估计被证明是一致的。估计的计算很简单。我们还提供了一种修正的权重函数以提高检验效能。广泛的模拟研究表明,精确置信区间具有准确的名义覆盖概率,并且所提出的点估计在实际样本量下几乎无偏。

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