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Bayesian selective response-adaptive design using the historical control.
Kim, Mi-Ok; Harun, Nusrat; Liu, Chunyan; Khoury, Jane C; Broderick, Joseph P.
Afiliação
  • Kim MO; UCSF Helen Diller Family Comprehensive Cancer Center, San Francisco, California, USA.
  • Harun N; Department of Epidemiology and Biostatistics, University of California San Francisco, San Francisco, California, USA.
  • Liu C; UCSF Helen Diller Family Comprehensive Cancer Center, San Francisco, California, USA.
  • Khoury JC; Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA.
  • Broderick JP; Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA.
Stat Med ; 37(26): 3709-3722, 2018 11 20.
Article em En | MEDLINE | ID: mdl-29900577
ABSTRACT
High quality historical control data, if incorporated, may reduce sample size, trial cost, and duration. A too optimistic use of the data, however, may result in bias under prior-data conflict. Motivated by well-publicized two-arm comparative trials in stroke, we propose a Bayesian design that both adaptively incorporates historical control data and selectively adapt the treatment allocation ratios within an ongoing trial responsively to the relative treatment effects. The proposed design differs from existing designs that borrow from historical controls. As opposed to reducing the number of subjects assigned to the control arm blindly, this design does so adaptively to the relative treatment effects only if evaluation of cumulated current trial data combined with the historical control suggests the superiority of the intervention arm. We used the effective historical sample size approach to quantify borrowed information on the control arm and modified the treatment allocation rules of the doubly adaptive biased coin design to incorporate the quantity. The modified allocation rules were then implemented under the Bayesian framework with commensurate priors addressing prior-data conflict. Trials were also more frequently concluded earlier in line with the underlying truth, reducing trial cost, and duration and yielded parameter estimates with smaller standard errors.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Projetos de Pesquisa / Teorema de Bayes Tipo de estudo: Clinical_trials / Prognostic_studies Idioma: En Revista: Stat Med Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Projetos de Pesquisa / Teorema de Bayes Tipo de estudo: Clinical_trials / Prognostic_studies Idioma: En Revista: Stat Med Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Estados Unidos