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模型不确定性下二元反应的概念验证与剂量估计

Proof of concept and dose estimation with binary responses under model uncertainty.

作者信息

Klingenberg B

机构信息

Department of Mathematics and Statistics, Williams College, Williamstown, MA 01267, USA.

出版信息

Stat Med. 2009 Jan 30;28(2):274-92. doi: 10.1002/sim.3477.

Abstract

This article suggests a unified framework for testing Proof of Concept (PoC) and estimating a target dose for the benefit of a more comprehensive, robust and powerful analysis in phase II or similar clinical trials. From a pre-specified set of candidate models, we choose the ones that best describe the observed dose-response. To decide which models, if any, significantly pick up a dose effect, we construct the permutation distribution of the minimum P-value over the candidate set. This allows us to find critical values and multiplicity adjusted P-values that control the familywise error rate of declaring any spurious effect in the candidate set as significant. Model averaging is then used to estimate a target dose. Popular single or multiple contrast tests for PoC, such as the Cochran-Armitage, Dunnett or Williams tests, are only optimal for specific dose-response shapes and do not provide target dose estimates with confidence limits. A thorough evaluation and comparison of our approach to these tests reveal that its power is as good or better in detecting a dose-response under various shapes with many more additional benefits: It incorporates model uncertainty in PoC decisions and target dose estimation, yields confidence intervals for target dose estimates and extends to more complicated data structures. We illustrate our method with the analysis of a Phase II clinical trial.

摘要

本文提出了一个统一框架,用于测试概念验证(PoC)并估计目标剂量,以利于在II期或类似临床试验中进行更全面、稳健和有力的分析。从一组预先指定的候选模型中,我们选择最能描述观察到的剂量反应的模型。为了确定哪些模型(如果有的话)能显著捕捉到剂量效应,我们构建了候选模型集中最小P值的排列分布。这使我们能够找到控制在候选集中将任何虚假效应宣布为显著的家族性错误率的临界值和经多重性调整的P值。然后使用模型平均法来估计目标剂量。用于PoC的常见单对比或多对比检验,如 Cochr an-Armitage检验、Dunnett检验或Williams检验,仅对特定的剂量反应形状是最优的,并且不能提供带有置信限的目标剂量估计。对我们的方法与这些检验进行全面评估和比较后发现,在检测各种形状的剂量反应时,我们方法的功效与之相当或更好,并且还有更多额外的优点:它在PoC决策和目标剂量估计中纳入了模型不确定性,产生目标剂量估计的置信区间,并可扩展到更复杂的数据结构。我们通过对一项II期临床试验的分析来说明我们的方法。

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