The ordinal endpoint is prevalent in clinical studies. For example, for the COVID-19, the most common endpoint used was 7-point ordinal scales. Another example is in phase II cancer studies, efficacy is often assessed as an ordinal variable based on a level of response of solid tumors with four categories: complete response, partial response, stable disease, and progression, though often a dichotomized approach is used in practices. However, there lack of designs for the ordinal endpoint despite Whitehead et al. (1993, 2017), Jaki et al. (2003) to list a few. In this paper, we propose a generic group sequential schema based on Bayesian methods for ordinal endpoints, including three methods, the proportional-odds-model (PO)-based, non-proportional-odds-model (NPO)-based, and PO/NPO switch-model-based designs, which makes our proposed methods generic to be able to deal with various scenarios. We conducted extensive simulations to demonstrate the desirable performances of the proposed method and an R package BayesOrdDesign has also been developed.
翻译:例如,对于COVID-19, 最常用的终点是7点点点点标度,另一个例子是第二阶段的癌症研究,根据四类固态肿瘤的反应水平,效率通常被评估为一种标准变量:完全反应、部分反应、稳定疾病和进化,尽管在实践中往往采用二分法方法;然而,尽管怀特黑德等人(1993年、2017年)、贾基等人(2003年),但缺乏对角端点的设计,因此无法列出几个。在本文件中,我们提议根据巴耶斯方法对角端点进行普通小组顺序规划,包括三种方法、基于比例值模型、非比例值模型和非比例值模型,以及PO/NPO的切换模型设计,这使得我们拟议的方法具有通用性,能够应对各种情景。我们进行了广泛的模拟,以展示拟议方法的适当性性能,并开发了R包包BayesOrDign。