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Joint model for left-censored longitudinal data, recurrent events and terminal event: Predictive abilities of tumor burden for cancer evolution with application to the FFCD 2000-05 trial.
Król, Agnieszka; Ferrer, Loïc; Pignon, Jean-Pierre; Proust-Lima, Cécile; Ducreux, Michel; Bouché, Olivier; Michiels, Stefan; Rondeau, Virginie.
Afiliación
  • Król A; University of Bordeaux, INSERM U1219, 146 rue Léo Saignat, 33076 Bordeaux Cedex, France. agnieszka.krol@isped.u-bordeaux2.fr.
  • Ferrer L; University of Bordeaux, INSERM U1219, 146 rue Léo Saignat, 33076 Bordeaux Cedex, France.
  • Pignon JP; INSERM U1018 CESP, Service de Biostatistique et d'Épidémiologie Gustave Roussy, U. Paris-Sud, 114 rue Édouard-Vaillant, 94805 Villejuif Cedex, France.
  • Proust-Lima C; University of Bordeaux, INSERM U1219, 146 rue Léo Saignat, 33076 Bordeaux Cedex, France.
  • Ducreux M; Medical Oncology, Gustave Roussy, U. Paris-Sud, 114 rue Édouard-Vaillant, 94805 Villejuif Cedex, France.
  • Bouché O; University Hospital, Hôpital Robert Debré, Avenue du Général Koenig, 51092 Reims Cedex, France.
  • Michiels S; INSERM U1018 CESP, Service de Biostatistique et d'Épidémiologie Gustave Roussy, U. Paris-Sud, 114 rue Édouard-Vaillant, 94805 Villejuif Cedex, France.
  • Rondeau V; University of Bordeaux, INSERM U1219, 146 rue Léo Saignat, 33076 Bordeaux Cedex, France.
Biometrics ; 72(3): 907-16, 2016 09.
Article en En | MEDLINE | ID: mdl-26890381
In oncology, the international WHO and RECIST criteria have allowed the standardization of tumor response evaluation in order to identify the time of disease progression. These semi-quantitative measurements are often used as endpoints in phase II and phase III trials to study the efficacy of new therapies. However, through categorization of the continuous tumor size, information can be lost and they can be challenged by recently developed methods of modeling biomarkers in a longitudinal way. Thus, it is of interest to compare the predictive ability of cancer progressions based on categorical criteria and quantitative measures of tumor size (left-censored due to detection limit problems) and/or appearance of new lesions on overall survival. We propose a joint model for a simultaneous analysis of three types of data: a longitudinal marker, recurrent events, and a terminal event. The model allows to determine in a randomized clinical trial on which particular component treatment acts mostly. A simulation study is performed and shows that the proposed trivariate model is appropriate for practical use. We propose statistical tools that evaluate predictive accuracy for joint models to compare our model to models based on categorical criteria and their components. We apply the model to a randomized phase III clinical trial of metastatic colorectal cancer, conducted by the Fédération Francophone de Cancérologie Digestive (FFCD 2000-05 trial), which assigned 410 patients to two therapeutic strategies with multiple successive chemotherapy regimens.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Valor Predictivo de las Pruebas / Modelos Estadísticos / Carga Tumoral Tipo de estudio: Clinical_trials / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Biometrics Año: 2016 Tipo del documento: Article País de afiliación: Francia

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Valor Predictivo de las Pruebas / Modelos Estadísticos / Carga Tumoral Tipo de estudio: Clinical_trials / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Biometrics Año: 2016 Tipo del documento: Article País de afiliación: Francia