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A SAS macro for target dose estimation by reinforced urn processes in phase I clinical trials.

机译:在I期临床试验中,通过增强的processes过程估算目标剂量的SAS宏。

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摘要

The reinforced urn processes (RUPs) approach can estimate the target dose on the basis of the prior distribution function precisely and conveniently without the requirements about the explicit-estimated dose-response curve and the posterior complicated inference. The application of the RUPs approach was not discussed from the perspective of phase I clinical trial in the previous studies which just focused on the theory and methodology. And the modification of the traditional RUPs design should be considered for the purposes of ethnics and efficiency. A SAS macro was designed to explore the appropriate parameter settings according to the simulation outcomes in different situations and apply the RUPs approach for two state processes in phase I clinical trail with the modified RUPs design. The posterior estimation can be obtained precisely and efficiently with application of SAS program following the appropriate workflow and determination rule which were described in the example.
机译:增强骨灰processes过程(RUPs)方法可以根据先验分布函数准确,方便地估计目标剂量,而无需明确估计剂量反应曲线和后验复杂推断。在以前的研究中,仅从理论和方法学角度出发,并未从I期临床试验的角度讨论RUPs方法的应用。并且出于种族和效率的目的,应考虑对传统RUP设计的修改。 SAS宏旨在根据不同情况下的模拟结果探索合适的参数设置,并使用改进的RUPs设计将RUPs方法应用于I期临床试验的两个状态过程。遵循示例中描述的适当工作流程和确定规则,通过使用SAS程序,可以精确高效地获得后验估计。

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