An R package for simulation experiments evaluating clinical trial designs.

Yuanyuan Wang, Roger Day
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引用次数: 0

Abstract

This paper presents an open-source application for evaluating competing clinical trial (CT) designs using simulations. The S4 system of classes and methods is utilized. Using object-oriented programming provides extensibility through careful, clear interface specification; using R, an open-source widely-used statistical language, makes the application extendible by the people who design CTs: biostatisticians. Four key classes define the specifications of the population models, CT designs, outcome models and evaluation criteria. Five key methods define the interfaces for generating patient baseline characteristics, stopping rule, assigning treatment, generating patient outcomes and calculating the criteria. Documentation of their connections with the user input screens, with the central simulation loop, and with each other faciliates the extensibility. New subclasses and instances of existing classes meeting these interfaces can integrate immediately into the application. To illustrate the application, we evaluate the effect of patient pharmacokinetic heterogeneity on the performance of a common Phase I "3+3" design.

Abstract Image

一个用于评估临床试验设计的模拟实验的R包。
本文提出了一个开源的应用程序,用于评估竞争的临床试验(CT)设计使用模拟。使用了S4类和方法系统。使用面向对象编程通过仔细、清晰的接口规范提供可扩展性;使用R,一种广泛使用的开源统计语言,使得设计ct的人:生物统计学家可以扩展应用程序。四个关键类别定义了总体模型、CT设计、结果模型和评估标准的规格。五个关键方法定义了生成患者基线特征、停止规则、分配治疗、生成患者结果和计算标准的接口。它们与用户输入屏幕、中央模拟循环以及彼此之间的连接的文档化有助于实现可扩展性。满足这些接口的新子类和现有类的实例可以立即集成到应用程序中。为了说明这一应用,我们评估了患者药代动力学异质性对普通I期“3+3”设计性能的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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