频数推理
贝叶斯概率
药物开发
计算机科学
风险分析(工程)
临床试验
过程(计算)
数据科学
贝叶斯推理
机器学习
数据挖掘
医学
药品
人工智能
药理学
病理
操作系统
作者
Stephen J. Ruberg,F. Beckers,Rob Hemmings,Peter Honig,Telba Irony,Lisa M. LaVange,Grazyna Liebérman,James Mayne,Richard Moscicki
标识
DOI:10.1038/s41573-023-00638-0
摘要
The pharmaceutical industry and its global regulators have routinely used frequentist statistical methods, such as null hypothesis significance testing and p values, for evaluation and approval of new treatments. The clinical drug development process, however, with its accumulation of data over time, can be well suited for the use of Bayesian statistical approaches that explicitly incorporate existing data into clinical trial design, analysis and decision-making. Such approaches, if used appropriately, have the potential to substantially reduce the time and cost of bringing innovative medicines to patients, as well as to reduce the exposure of patients in clinical trials to ineffective or unsafe treatment regimens. Nevertheless, despite advances in Bayesian methodology, the availability of the necessary computational power and growing amounts of relevant existing data that could be used, Bayesian methods remain underused in the clinical development and regulatory review of new therapies. Here, we highlight the value of Bayesian methods in drug development, discuss barriers to their application and recommend approaches to address them. Our aim is to engage stakeholders in the process of considering when the use of existing data is appropriate and how Bayesian methods can be implemented more routinely as an effective tool for doing so.
科研通智能强力驱动
Strongly Powered by AbleSci AI