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Crude incidence in two-phase designs in the presence of competing risks

BACKGROUND: In many studies, some information might not be available for the whole cohort, some covariates, or even the outcome, might be ascertained in selected subsamples. These studies are part of a broad category termed two-phase studies. Common examples include the nested case-control and the c...

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Autores principales: Rebora, Paola, Antolini, Laura, Glidden, David V., Valsecchi, Maria Grazia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4710022/
https://www.ncbi.nlm.nih.gov/pubmed/26754746
http://dx.doi.org/10.1186/s12874-015-0103-1
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author Rebora, Paola
Antolini, Laura
Glidden, David V.
Valsecchi, Maria Grazia
author_facet Rebora, Paola
Antolini, Laura
Glidden, David V.
Valsecchi, Maria Grazia
author_sort Rebora, Paola
collection PubMed
description BACKGROUND: In many studies, some information might not be available for the whole cohort, some covariates, or even the outcome, might be ascertained in selected subsamples. These studies are part of a broad category termed two-phase studies. Common examples include the nested case-control and the case-cohort designs. For two-phase studies, appropriate weighted survival estimates have been derived; however, no estimator of cumulative incidence accounting for competing events has been proposed. This is relevant in the presence of multiple types of events, where estimation of event type specific quantities are needed for evaluating outcome. METHODS: We develop a non parametric estimator of the cumulative incidence function of events accounting for possible competing events. It handles a general sampling design by weights derived from the sampling probabilities. The variance is derived from the influence function of the subdistribution hazard. RESULTS: The proposed method shows good performance in simulations. It is applied to estimate the crude incidence of relapse in childhood acute lymphoblastic leukemia in groups defined by a genotype not available for everyone in a cohort of nearly 2000 patients, where death due to toxicity acted as a competing event. In a second example the aim was to estimate engagement in care of a cohort of HIV patients in resource limited setting, where for some patients the outcome itself was missing due to lost to follow-up. A sampling based approach was used to identify outcome in a subsample of lost patients and to obtain a valid estimate of connection to care. CONCLUSIONS: A valid estimator for cumulative incidence of events accounting for competing risks under a general sampling design from an infinite target population is derived.
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spelling pubmed-47100222016-01-13 Crude incidence in two-phase designs in the presence of competing risks Rebora, Paola Antolini, Laura Glidden, David V. Valsecchi, Maria Grazia BMC Med Res Methodol Technical Advance BACKGROUND: In many studies, some information might not be available for the whole cohort, some covariates, or even the outcome, might be ascertained in selected subsamples. These studies are part of a broad category termed two-phase studies. Common examples include the nested case-control and the case-cohort designs. For two-phase studies, appropriate weighted survival estimates have been derived; however, no estimator of cumulative incidence accounting for competing events has been proposed. This is relevant in the presence of multiple types of events, where estimation of event type specific quantities are needed for evaluating outcome. METHODS: We develop a non parametric estimator of the cumulative incidence function of events accounting for possible competing events. It handles a general sampling design by weights derived from the sampling probabilities. The variance is derived from the influence function of the subdistribution hazard. RESULTS: The proposed method shows good performance in simulations. It is applied to estimate the crude incidence of relapse in childhood acute lymphoblastic leukemia in groups defined by a genotype not available for everyone in a cohort of nearly 2000 patients, where death due to toxicity acted as a competing event. In a second example the aim was to estimate engagement in care of a cohort of HIV patients in resource limited setting, where for some patients the outcome itself was missing due to lost to follow-up. A sampling based approach was used to identify outcome in a subsample of lost patients and to obtain a valid estimate of connection to care. CONCLUSIONS: A valid estimator for cumulative incidence of events accounting for competing risks under a general sampling design from an infinite target population is derived. BioMed Central 2016-01-11 /pmc/articles/PMC4710022/ /pubmed/26754746 http://dx.doi.org/10.1186/s12874-015-0103-1 Text en © Rebora et al. 2016 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License(http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver(http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Technical Advance
Rebora, Paola
Antolini, Laura
Glidden, David V.
Valsecchi, Maria Grazia
Crude incidence in two-phase designs in the presence of competing risks
title Crude incidence in two-phase designs in the presence of competing risks
title_full Crude incidence in two-phase designs in the presence of competing risks
title_fullStr Crude incidence in two-phase designs in the presence of competing risks
title_full_unstemmed Crude incidence in two-phase designs in the presence of competing risks
title_short Crude incidence in two-phase designs in the presence of competing risks
title_sort crude incidence in two-phase designs in the presence of competing risks
topic Technical Advance
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4710022/
https://www.ncbi.nlm.nih.gov/pubmed/26754746
http://dx.doi.org/10.1186/s12874-015-0103-1
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