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Aspirin and other non-steroidal anti-inflammatory drug use and colorectal cancer survival: a cohort study

BACKGROUND: Aspirin has been widely reported to reduce the incidence of colorectal cancer. Recently, a survival benefit after diagnosis has also been suggested. Data regarding such a benefit are to date contradictory. This study examines the effect of non-steroidal anti-inflammatory drug (NSAID) use...

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Autores principales: Walker, A J, Grainge, M J, Card, T R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3493766/
https://www.ncbi.nlm.nih.gov/pubmed/23011483
http://dx.doi.org/10.1038/bjc.2012.427
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author Walker, A J
Grainge, M J
Card, T R
author_facet Walker, A J
Grainge, M J
Card, T R
author_sort Walker, A J
collection PubMed
description BACKGROUND: Aspirin has been widely reported to reduce the incidence of colorectal cancer. Recently, a survival benefit after diagnosis has also been suggested. Data regarding such a benefit are to date contradictory. This study examines the effect of non-steroidal anti-inflammatory drug (NSAID) use on mortality in colorectal cancer in a larger patient cohort than previously to further clarify this effect, especially in terms of exposure timing and dosing. METHODS: A study using the General Practice Research Database assessed whether aspirin or NSAID exposure in the year immediately following diagnosis affected all-cause mortality in a cohort of 13 994 colorectal cancer patients. Cox proportional hazards modelling adjusted for age, gender, smoking, body mass index and comorbidity. RESULTS: Overall mortality was slightly lower in patients treated with aspirin, (hazard ratio (HR)=0.91; 95% confidence interval (CI)=0.82–1.00). This effect was observed only in patients treated with prophylaxis-dose aspirin (HR=0.89, CI=0.80–0.98) and only in patients taking aspirin before diagnosis (HR=0.86, CI=0.76–0.98). Differential effects were observed depending on the time after diagnosis. Up to 5 years, a reduction in mortality was observed for aspirin users (HR=0.83, CI=0.75–0.92), whereas after 10 years there was an increase in mortality (HR=1.94, CI=1.26–2.99). For NSAID use, no significant effect was observed on overall mortality (HR=1.07, CI=0.98–1.15). High-dose NSAID use was associated with a slight increase in mortality (HR=1.41, CI=1.26–1.56). INTERPRETATION: These findings provide further indication that aspirin may be beneficial in reducing mortality in colorectal cancer during the first 5 years. The same cannot be said for other NSAIDs, where a small increase in mortality was observed.
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spelling pubmed-34937662013-10-23 Aspirin and other non-steroidal anti-inflammatory drug use and colorectal cancer survival: a cohort study Walker, A J Grainge, M J Card, T R Br J Cancer Epidemiology BACKGROUND: Aspirin has been widely reported to reduce the incidence of colorectal cancer. Recently, a survival benefit after diagnosis has also been suggested. Data regarding such a benefit are to date contradictory. This study examines the effect of non-steroidal anti-inflammatory drug (NSAID) use on mortality in colorectal cancer in a larger patient cohort than previously to further clarify this effect, especially in terms of exposure timing and dosing. METHODS: A study using the General Practice Research Database assessed whether aspirin or NSAID exposure in the year immediately following diagnosis affected all-cause mortality in a cohort of 13 994 colorectal cancer patients. Cox proportional hazards modelling adjusted for age, gender, smoking, body mass index and comorbidity. RESULTS: Overall mortality was slightly lower in patients treated with aspirin, (hazard ratio (HR)=0.91; 95% confidence interval (CI)=0.82–1.00). This effect was observed only in patients treated with prophylaxis-dose aspirin (HR=0.89, CI=0.80–0.98) and only in patients taking aspirin before diagnosis (HR=0.86, CI=0.76–0.98). Differential effects were observed depending on the time after diagnosis. Up to 5 years, a reduction in mortality was observed for aspirin users (HR=0.83, CI=0.75–0.92), whereas after 10 years there was an increase in mortality (HR=1.94, CI=1.26–2.99). For NSAID use, no significant effect was observed on overall mortality (HR=1.07, CI=0.98–1.15). High-dose NSAID use was associated with a slight increase in mortality (HR=1.41, CI=1.26–1.56). INTERPRETATION: These findings provide further indication that aspirin may be beneficial in reducing mortality in colorectal cancer during the first 5 years. The same cannot be said for other NSAIDs, where a small increase in mortality was observed. Nature Publishing Group 2012-10-23 2012-09-25 /pmc/articles/PMC3493766/ /pubmed/23011483 http://dx.doi.org/10.1038/bjc.2012.427 Text en Copyright © 2012 Cancer Research UK https://creativecommons.org/licenses/by-nc-sa/3.0/From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/
spellingShingle Epidemiology
Walker, A J
Grainge, M J
Card, T R
Aspirin and other non-steroidal anti-inflammatory drug use and colorectal cancer survival: a cohort study
title Aspirin and other non-steroidal anti-inflammatory drug use and colorectal cancer survival: a cohort study
title_full Aspirin and other non-steroidal anti-inflammatory drug use and colorectal cancer survival: a cohort study
title_fullStr Aspirin and other non-steroidal anti-inflammatory drug use and colorectal cancer survival: a cohort study
title_full_unstemmed Aspirin and other non-steroidal anti-inflammatory drug use and colorectal cancer survival: a cohort study
title_short Aspirin and other non-steroidal anti-inflammatory drug use and colorectal cancer survival: a cohort study
title_sort aspirin and other non-steroidal anti-inflammatory drug use and colorectal cancer survival: a cohort study
topic Epidemiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3493766/
https://www.ncbi.nlm.nih.gov/pubmed/23011483
http://dx.doi.org/10.1038/bjc.2012.427
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