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具有二元终点的适应性单臂两阶段临床试验的有效置信限

Efficient confidence limits for adaptive one-arm two-stage clinical trials with binary endpoints.

作者信息

Shan Guogen, Zhang Hua, Jiang Tao

机构信息

Epidemiology and Biostatistics Program, Department of Environmental and Occupational Health, School of Community Health Sciences, University of Nevada Las Vegas, Las Vegas, 89154, NV, USA.

School of Computer and Information Engineering, Zhejiang Gongshang University, Hangzhou, 310018, Zhejiang, China.

出版信息

BMC Med Res Methodol. 2017 Feb 6;17(1):22. doi: 10.1186/s12874-017-0297-5.

Abstract

BACKGROUND

Recently, several adaptive one-arm two-stage designs have been developed by fully using the information from previous stages to reduce the expected sample size in clinical trials with binary endpoints as primary outcome. It is important to compute exact confidence limits for these studies.

METHODS

In this article, we propose three new one-sided limits by ordering the sample space based on p-value, average response rate at each stage, and asymptotic lower limit, as compared to another three existing sample size ordering approaches based on average response rate. Among the three proposed approaches, the one based on the average response rate at each stage is not exact, and the remaining two approaches are exact with the coverage probability guaranteed.

RESULTS

We compare these exact intervals by using the two commonly used criteria: simple average length and expected length. The existing three approaches based on average response rate have similar performance, and they have shorter expected lengths than the two proposed exact approaches although the gain is small, while this trend is reversed under the simple average criterion.

CONCLUSIONS

We would recommend the two exact proposed approaches based on p-value and asymptotic lower limit under the simple average length criterion, and the approach based on average response rate under the expected length criterion.

摘要

背景

最近,通过充分利用前期阶段的信息,已经开发出了几种适应性单臂两阶段设计,以减少以二元终点作为主要结局的临床试验中的预期样本量。为这些研究计算精确的置信区间很重要。

方法

在本文中,与另外三种基于平均反应率的现有样本量排序方法相比,我们通过基于p值、各阶段的平均反应率和渐近下限对样本空间进行排序,提出了三个新的单侧界限。在所提出的三种方法中,基于各阶段平均反应率的方法并不精确,其余两种方法是精确的,且保证了覆盖概率。

结果

我们使用两个常用标准比较这些精确区间:简单平均长度和预期长度。现有的三种基于平均反应率的方法具有相似的性能,并且它们的预期长度比所提出的两种精确方法短,尽管增益很小,而在简单平均标准下这种趋势则相反。

结论

在简单平均长度标准下,我们推荐基于p值和渐近下限的两种精确方法,以及在预期长度标准下基于平均反应率的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/43f7/5294881/8a82a5ba8a1c/12874_2017_297_Fig1_HTML.jpg

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