Your browser doesn't support javascript.
loading
Uncertainty directed factorial clinical trials.
Kotecha, Gopal; Ventz, Steffen; Fortini, Sandra; Trippa, Lorenzo.
Afiliación
  • Kotecha G; Department of Biostatistics, Harvard School of Public Health, 677 Huntington Ave, Boston, MA, 02115, USA.
  • Ventz S; Department of Data Science, Dana-Farber Cancer Institute, 450 Brookline Ave, CLSB 11007, Boston, MA, 02215, USA.
  • Fortini S; Division of Biostatistics, School of Public Health, University of Minnesota, University Office Plaza, Ste 200, 2221 University Ave SE, Minneapolis, MN 55414, USA.
  • Trippa L; Department of Decision Sciences, Bocconi University, Via Röntgen, 1, 20136 Milano, Italy.
Biostatistics ; 25(3): 833-851, 2024 Jul 01.
Article en En | MEDLINE | ID: mdl-38330084
ABSTRACT
The development and evaluation of novel treatment combinations is a key component of modern clinical research. The primary goals of factorial clinical trials of treatment combinations range from the estimation of intervention-specific effects, or the discovery of potential synergies, to the identification of combinations with the highest response probabilities. Most factorial studies use balanced or block randomization, with an equal number of patients assigned to each treatment combination, irrespective of the specific goals of the trial. Here, we introduce a class of Bayesian response-adaptive designs for factorial clinical trials with binary outcomes. The study design was developed using Bayesian decision-theoretic arguments and adapts the randomization probabilities to treatment combinations during the enrollment period based on the available data. Our approach enables the investigator to specify a utility function representative of the aims of the trial, and the Bayesian response-adaptive randomization algorithm aims to maximize this utility function. We considered several utility functions and factorial designs tailored to them. Then, we conducted a comparative simulation study to illustrate relevant differences of key operating characteristics across the resulting designs. We also investigated the asymptotic behavior of the proposed adaptive designs. We also used data summaries from three recent factorial trials in perioperative care, smoking cessation, and infectious disease prevention to define realistic simulation scenarios and illustrate advantages of the introduced trial designs compared to other study designs.
Asunto(s)
Palabras clave

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Teorema de Bayes Tipo de estudio: Clinical_trials / Prognostic_studies Límite: Humans Idioma: En Revista: Biostatistics Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Teorema de Bayes Tipo de estudio: Clinical_trials / Prognostic_studies Límite: Humans Idioma: En Revista: Biostatistics Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos