Whitehead, John and Patterson, Scott and Webber, Dawn and Zhou, Yinghui (2001) Easy-to-implement Bayesian methods for dose-escalation studies in healthy volunteers. Biostatistics, 2 (1). pp. 47-61. ISSN 1468-4357Full text not available from this repository.
In phase I clinical trials, experimental drugs are administered to healthy volunteers in order to establish their safety and to explore the relationship between the dose taken and the concentration found in plasma. Each volunteer receives a series of increasing single doses. In this paper a Bayesian decision procedure is developed for choosing the doses to give in the next round of the study, taking into account both prior information and the responses observed so far. The procedure seeks the optimal doses for learning about the dose–concentration relationship, subject to a constraint which reduces the risk of administering dangerously high doses. Individual volunteers receive more than one dose, and the pharmacokinetic responses observed are, after logarithmic transformation, treated as approximately normally distributed. Thus data analysis can be achieved by fitting linear mixed models. By expressing prior information as ‘pseudo-data’, and by maximizing over posterior distributions rather than taking expectations, a procedure which can be implemented using standard mixed model software is derived. Comparisons are made with existing approaches to the conduct of these studies, and the new method is illustrated using real and simulated data.
|Journal or Publication Title:||Biostatistics|
|Additional Information:||RAE_import_type : Journal article RAE_uoa_type : Statistics and Operational Research|
|Uncontrolled Keywords:||Bayesian decision procedure ; Dose-escalation ; First-into-man ; Pharmacokinetics ; Phase I trial.|
|Subjects:||Q Science > QA Mathematics|
|Departments:||Faculty of Science and Technology > Mathematics and Statistics|
|Deposited On:||29 Mar 2008 12:21|
|Last Modified:||21 May 2016 00:01|
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