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Flexible two-stage design with sample size reassessment for survival trials.
Desseaux, K; Porcher, R.
Afiliação
  • Desseaux K; Inserm U717, Département de Biostatistique et Informatique Médicale, Hôpital Saint-Louis, AP-HP, Université Paris 7, Paris, France. kristell.desseaux@univ-paris-diderot.fr
Stat Med ; 26(27): 5002-13, 2007 Nov 30.
Article em En | MEDLINE | ID: mdl-17577242
Flexible trials with adaptive design modification at interim analyses have been recently proposed as an answer to cope with some limitations of traditional designs for phase III trials. Actually, the sample size and duration of fixed design trials strongly depend on the determination, prior to the study, of key parameters such as the expected treatment effect and the event rates. A misspecification of these parameters may result in an underpowered or overpowered trial. In the flexible framework, the remainder of a design can be modified at an interim analysis, while preserving the initially specified global error rates. In this work, we present a flexible design with sample size re-evaluation for survival trials and study its properties in practical settings. The results show that, if parameters are initially misspecified, the proposed method allows an improved power control with a reasonable increase in sample size, if any. Practical guidelines concerning the choice of the trial parameters are also given.
Assuntos
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Projetos de Pesquisa / Análise de Sobrevida / Ensaios Clínicos como Assunto / Tamanho da Amostra Tipo de estudo: Guideline / Prognostic_studies Limite: Humans Idioma: En Revista: Stat Med Ano de publicação: 2007 Tipo de documento: Article
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Projetos de Pesquisa / Análise de Sobrevida / Ensaios Clínicos como Assunto / Tamanho da Amostra Tipo de estudo: Guideline / Prognostic_studies Limite: Humans Idioma: En Revista: Stat Med Ano de publicação: 2007 Tipo de documento: Article