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Non Melanoma Skin Cancer and Subsequent Cancer Risk

INTRODUCTION: Several studies have shown an increased risk of cancer after non melanoma skin cancers (NMSC) but the individual risk factors underlying this risk have not been elucidated, especially in relation to sun exposure and skin sensitivity to sunlight. PURPOSE: The aim of this study was to ex...

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Autores principales: Rees, Judy R., Zens, M. Scot, Gui, Jiang, Celaya, Maria O., Riddle, Bruce L., Karagas, Margaret R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4061037/
https://www.ncbi.nlm.nih.gov/pubmed/24937304
http://dx.doi.org/10.1371/journal.pone.0099674
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author Rees, Judy R.
Zens, M. Scot
Gui, Jiang
Celaya, Maria O.
Riddle, Bruce L.
Karagas, Margaret R.
author_facet Rees, Judy R.
Zens, M. Scot
Gui, Jiang
Celaya, Maria O.
Riddle, Bruce L.
Karagas, Margaret R.
author_sort Rees, Judy R.
collection PubMed
description INTRODUCTION: Several studies have shown an increased risk of cancer after non melanoma skin cancers (NMSC) but the individual risk factors underlying this risk have not been elucidated, especially in relation to sun exposure and skin sensitivity to sunlight. PURPOSE: The aim of this study was to examine the individual risk factors associated with the development of subsequent cancers after non melanoma skin cancer. METHODS: Participants in the population-based New Hampshire Skin Cancer Study provided detailed risk factor data, and subsequent cancers were identified via linkage with the state cancer registry. Deaths were identified via state and national death records. A Cox proportional hazard model was used to estimate risk of subsequent malignancies in NMSC patients versus controls and to assess the potential confounding effects of multiple risk factors on this risk. RESULTS: Among 3584 participants, risk of a subsequent cancer (other than NMSC) was higher after basal cell carcinoma (BCC) (adjusted HR 1.40 [95% CI 1.15, 1.71]) than squamous cell carcinoma (SCC) (adjusted HR 1.18 [95% CI 0.95, 1.46]) compared to controls (adjusted for age, sex and current cigarette smoking). After SCC, risk was higher among those diagnosed before age 60 (HR 1.96 [95% CI 1.24, 3.12]). An over 3-fold risk of melanoma after SCC (HR 3.62; 95% CI 1.85, 7.11) and BCC (HR 3.28; 95% CI 1.66, 6.51) was observed, even after further adjustment for sun exposure-related factors and family history of skin cancer. In men, prostate cancer incidence was higher after BCC compared to controls (HR 1.64; 95% CI 1.10, 2.46). CONCLUSIONS: Our population-based study indicates an increased cancer risk after NMSC that cannot be fully explained by known cancer risk factors.
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spelling pubmed-40610372014-06-20 Non Melanoma Skin Cancer and Subsequent Cancer Risk Rees, Judy R. Zens, M. Scot Gui, Jiang Celaya, Maria O. Riddle, Bruce L. Karagas, Margaret R. PLoS One Research Article INTRODUCTION: Several studies have shown an increased risk of cancer after non melanoma skin cancers (NMSC) but the individual risk factors underlying this risk have not been elucidated, especially in relation to sun exposure and skin sensitivity to sunlight. PURPOSE: The aim of this study was to examine the individual risk factors associated with the development of subsequent cancers after non melanoma skin cancer. METHODS: Participants in the population-based New Hampshire Skin Cancer Study provided detailed risk factor data, and subsequent cancers were identified via linkage with the state cancer registry. Deaths were identified via state and national death records. A Cox proportional hazard model was used to estimate risk of subsequent malignancies in NMSC patients versus controls and to assess the potential confounding effects of multiple risk factors on this risk. RESULTS: Among 3584 participants, risk of a subsequent cancer (other than NMSC) was higher after basal cell carcinoma (BCC) (adjusted HR 1.40 [95% CI 1.15, 1.71]) than squamous cell carcinoma (SCC) (adjusted HR 1.18 [95% CI 0.95, 1.46]) compared to controls (adjusted for age, sex and current cigarette smoking). After SCC, risk was higher among those diagnosed before age 60 (HR 1.96 [95% CI 1.24, 3.12]). An over 3-fold risk of melanoma after SCC (HR 3.62; 95% CI 1.85, 7.11) and BCC (HR 3.28; 95% CI 1.66, 6.51) was observed, even after further adjustment for sun exposure-related factors and family history of skin cancer. In men, prostate cancer incidence was higher after BCC compared to controls (HR 1.64; 95% CI 1.10, 2.46). CONCLUSIONS: Our population-based study indicates an increased cancer risk after NMSC that cannot be fully explained by known cancer risk factors. Public Library of Science 2014-06-17 /pmc/articles/PMC4061037/ /pubmed/24937304 http://dx.doi.org/10.1371/journal.pone.0099674 Text en © 2014 Rees et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Rees, Judy R.
Zens, M. Scot
Gui, Jiang
Celaya, Maria O.
Riddle, Bruce L.
Karagas, Margaret R.
Non Melanoma Skin Cancer and Subsequent Cancer Risk
title Non Melanoma Skin Cancer and Subsequent Cancer Risk
title_full Non Melanoma Skin Cancer and Subsequent Cancer Risk
title_fullStr Non Melanoma Skin Cancer and Subsequent Cancer Risk
title_full_unstemmed Non Melanoma Skin Cancer and Subsequent Cancer Risk
title_short Non Melanoma Skin Cancer and Subsequent Cancer Risk
title_sort non melanoma skin cancer and subsequent cancer risk
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4061037/
https://www.ncbi.nlm.nih.gov/pubmed/24937304
http://dx.doi.org/10.1371/journal.pone.0099674
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