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Colorectal cancer prevention by non-steroidal anti-inflammatory drugs: effects of dosage and timing

Epidemiological studies show that non-steroidal anti-inflammatory drugs (NSAIDs) reduce colorectal cancer incidence. We measured the rate ratio for colorectal adenocarcinoma according to dosage and the timing of exposure by means of a case–control study, nested in a non-concurrent cohort linkage stu...

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Autores principales: Collet, J-P, Sharpe, C, Belzile, E, Boivin, J-F, Hanley, J, Abenhaim, L
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 1999
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2374346/
https://www.ncbi.nlm.nih.gov/pubmed/10487613
http://dx.doi.org/10.1038/sj.bjc.6690651
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author Collet, J-P
Sharpe, C
Belzile, E
Boivin, J-F
Hanley, J
Abenhaim, L
author_facet Collet, J-P
Sharpe, C
Belzile, E
Boivin, J-F
Hanley, J
Abenhaim, L
author_sort Collet, J-P
collection PubMed
description Epidemiological studies show that non-steroidal anti-inflammatory drugs (NSAIDs) reduce colorectal cancer incidence. We measured the rate ratio for colorectal adenocarcinoma according to dosage and the timing of exposure by means of a case–control study, nested in a non-concurrent cohort linkage study, using the population of beneficiaries of the Saskatchewan Prescription Drug Plan from 1981 to 1995 with no history of cancer since 1970 as the source population. Four controls per case, matched on age and gender and alive when the case was diagnosed, were randomly selected. Dispensing rates, calculated over successive time periods, characterized NSAID exposure. We accrued 3844 cases of colon cancer and 1971 cases of rectal cancer. For colon cancer a significant trend towards a decreasing rate ratio was associated with increasing exposure during the 6 months preceding diagnosis (P-trend = 0.002). For both cancers, significant trends were associated with exposure 11–15 years before diagnosis (colon: P-trend = 0.01; rectum: P-trend = 0.0001). At the highest exposure levels the rate ratio for colon cancer was 0.57 (95% confidence interval (CI) 0.36–0.89); for rectal cancer it was 0.26 (95% CI 0.11–0.61). No protection was associated with exposure during other periods. The timing of NSAID use must be considered in planning intervention trials to prevent colorectal cancer. There may be a 10-year delay before any preventive effect will appear. © 1999 Cancer Research Campaign
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spelling pubmed-23743462009-09-10 Colorectal cancer prevention by non-steroidal anti-inflammatory drugs: effects of dosage and timing Collet, J-P Sharpe, C Belzile, E Boivin, J-F Hanley, J Abenhaim, L Br J Cancer Regular Article Epidemiological studies show that non-steroidal anti-inflammatory drugs (NSAIDs) reduce colorectal cancer incidence. We measured the rate ratio for colorectal adenocarcinoma according to dosage and the timing of exposure by means of a case–control study, nested in a non-concurrent cohort linkage study, using the population of beneficiaries of the Saskatchewan Prescription Drug Plan from 1981 to 1995 with no history of cancer since 1970 as the source population. Four controls per case, matched on age and gender and alive when the case was diagnosed, were randomly selected. Dispensing rates, calculated over successive time periods, characterized NSAID exposure. We accrued 3844 cases of colon cancer and 1971 cases of rectal cancer. For colon cancer a significant trend towards a decreasing rate ratio was associated with increasing exposure during the 6 months preceding diagnosis (P-trend = 0.002). For both cancers, significant trends were associated with exposure 11–15 years before diagnosis (colon: P-trend = 0.01; rectum: P-trend = 0.0001). At the highest exposure levels the rate ratio for colon cancer was 0.57 (95% confidence interval (CI) 0.36–0.89); for rectal cancer it was 0.26 (95% CI 0.11–0.61). No protection was associated with exposure during other periods. The timing of NSAID use must be considered in planning intervention trials to prevent colorectal cancer. There may be a 10-year delay before any preventive effect will appear. © 1999 Cancer Research Campaign Nature Publishing Group 1999-09 /pmc/articles/PMC2374346/ /pubmed/10487613 http://dx.doi.org/10.1038/sj.bjc.6690651 Text en Copyright © 1999 Cancer Research Campaign https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/.
spellingShingle Regular Article
Collet, J-P
Sharpe, C
Belzile, E
Boivin, J-F
Hanley, J
Abenhaim, L
Colorectal cancer prevention by non-steroidal anti-inflammatory drugs: effects of dosage and timing
title Colorectal cancer prevention by non-steroidal anti-inflammatory drugs: effects of dosage and timing
title_full Colorectal cancer prevention by non-steroidal anti-inflammatory drugs: effects of dosage and timing
title_fullStr Colorectal cancer prevention by non-steroidal anti-inflammatory drugs: effects of dosage and timing
title_full_unstemmed Colorectal cancer prevention by non-steroidal anti-inflammatory drugs: effects of dosage and timing
title_short Colorectal cancer prevention by non-steroidal anti-inflammatory drugs: effects of dosage and timing
title_sort colorectal cancer prevention by non-steroidal anti-inflammatory drugs: effects of dosage and timing
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2374346/
https://www.ncbi.nlm.nih.gov/pubmed/10487613
http://dx.doi.org/10.1038/sj.bjc.6690651
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