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Competing risk models to estimate the excess mortality and the first recurrent-event hazards

BACKGROUND: In medical research, one common competing risks situation is the study of different types of events, such as disease recurrence and death. We focused on that situation but considered death under two aspects: "expected death" and "excess death", the latter could be dir...

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Autores principales: Belot, Aurélien, Remontet, Laurent, Launoy, Guy, Jooste, Valérie, Giorgi, Roch
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3123657/
https://www.ncbi.nlm.nih.gov/pubmed/21612632
http://dx.doi.org/10.1186/1471-2288-11-78
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author Belot, Aurélien
Remontet, Laurent
Launoy, Guy
Jooste, Valérie
Giorgi, Roch
author_facet Belot, Aurélien
Remontet, Laurent
Launoy, Guy
Jooste, Valérie
Giorgi, Roch
author_sort Belot, Aurélien
collection PubMed
description BACKGROUND: In medical research, one common competing risks situation is the study of different types of events, such as disease recurrence and death. We focused on that situation but considered death under two aspects: "expected death" and "excess death", the latter could be directly or indirectly associated with the disease. METHODS: The excess hazard method allows estimating an excess mortality hazard using the population (expected) mortality hazard. We propose models combining the competing risks approach and the excess hazard method. These models are based on a joint modelling of each event-specific hazard, including the event-free excess death hazard. The proposed models are parsimonious, allow time-dependent hazard ratios, and facilitate comparisons between event-specific hazards and between covariate effects on different events. In a simulation study, we assessed the performance of the estimators and showed their good properties with different drop-out censoring rates and different sample sizes. RESULTS: We analyzed a population-based dataset on French colon cancer patients who have undergone curative surgery. Considering three competing events (local recurrence, distant metastasis, and death), we showed that the recurrence-free excess mortality hazard reached zero six months after treatment. Covariates sex, age, and cancer stage had the same effects on local recurrence and distant metastasis but a different effect on excess mortality. CONCLUSIONS: The proposed models consider the excess mortality within the framework of competing risks. Moreover, the joint estimation of the parameters allow (i) direct comparisons between covariate effects, and (ii) fitting models with common parameters to obtain more parsimonious models and more efficient parameter estimators.
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spelling pubmed-31236572011-06-26 Competing risk models to estimate the excess mortality and the first recurrent-event hazards Belot, Aurélien Remontet, Laurent Launoy, Guy Jooste, Valérie Giorgi, Roch BMC Med Res Methodol Research Article BACKGROUND: In medical research, one common competing risks situation is the study of different types of events, such as disease recurrence and death. We focused on that situation but considered death under two aspects: "expected death" and "excess death", the latter could be directly or indirectly associated with the disease. METHODS: The excess hazard method allows estimating an excess mortality hazard using the population (expected) mortality hazard. We propose models combining the competing risks approach and the excess hazard method. These models are based on a joint modelling of each event-specific hazard, including the event-free excess death hazard. The proposed models are parsimonious, allow time-dependent hazard ratios, and facilitate comparisons between event-specific hazards and between covariate effects on different events. In a simulation study, we assessed the performance of the estimators and showed their good properties with different drop-out censoring rates and different sample sizes. RESULTS: We analyzed a population-based dataset on French colon cancer patients who have undergone curative surgery. Considering three competing events (local recurrence, distant metastasis, and death), we showed that the recurrence-free excess mortality hazard reached zero six months after treatment. Covariates sex, age, and cancer stage had the same effects on local recurrence and distant metastasis but a different effect on excess mortality. CONCLUSIONS: The proposed models consider the excess mortality within the framework of competing risks. Moreover, the joint estimation of the parameters allow (i) direct comparisons between covariate effects, and (ii) fitting models with common parameters to obtain more parsimonious models and more efficient parameter estimators. BioMed Central 2011-05-25 /pmc/articles/PMC3123657/ /pubmed/21612632 http://dx.doi.org/10.1186/1471-2288-11-78 Text en Copyright ©2011 Belot et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Belot, Aurélien
Remontet, Laurent
Launoy, Guy
Jooste, Valérie
Giorgi, Roch
Competing risk models to estimate the excess mortality and the first recurrent-event hazards
title Competing risk models to estimate the excess mortality and the first recurrent-event hazards
title_full Competing risk models to estimate the excess mortality and the first recurrent-event hazards
title_fullStr Competing risk models to estimate the excess mortality and the first recurrent-event hazards
title_full_unstemmed Competing risk models to estimate the excess mortality and the first recurrent-event hazards
title_short Competing risk models to estimate the excess mortality and the first recurrent-event hazards
title_sort competing risk models to estimate the excess mortality and the first recurrent-event hazards
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3123657/
https://www.ncbi.nlm.nih.gov/pubmed/21612632
http://dx.doi.org/10.1186/1471-2288-11-78
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