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Nested case–control study of the effects of non-steroidal anti-inflammatory drugs on breast cancer risk and stage

We carried out a nested case–control study to measure the rate ratio (RR) for invasive female breast cancer in relation to non-steroidal anti-inflammatory drug (NSAID) use. The source population consisted of the female beneficiaries of the Saskatchewan Prescription Drug Plan from 1981 to 1995 with n...

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Autores principales: Sharpe, C R, Collet, J-P, McNutt, M, Belzile, E, Boivin, J-F, Hanley, J A
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2000
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2374529/
https://www.ncbi.nlm.nih.gov/pubmed/10883678
http://dx.doi.org/10.1054/bjoc.2000.1119
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author Sharpe, C R
Collet, J-P
McNutt, M
Belzile, E
Boivin, J-F
Hanley, J A
author_facet Sharpe, C R
Collet, J-P
McNutt, M
Belzile, E
Boivin, J-F
Hanley, J A
author_sort Sharpe, C R
collection PubMed
description We carried out a nested case–control study to measure the rate ratio (RR) for invasive female breast cancer in relation to non-steroidal anti-inflammatory drug (NSAID) use. The source population consisted of the female beneficiaries of the Saskatchewan Prescription Drug Plan from 1981 to 1995 with no history of cancer since 1970. Four controls/case, matched on age and sampling time, were randomly selected. Dispensing rates during successive time periods characterized NSAID exposure. RRs associated with exposure during each period were adjusted for exposure during the others. Confounding by other determinants was studied in analyses adjusted with data obtained by interviewing samples of subjects accrued from mid-1991 to mid-1995. We accrued 5882 cases and 23 517 controls. Increasing NSAID exposure 2–5 years preceding diagnosis was associated with a trend towards a decreasing RR (P -trend = 0.003); for the highest exposure level RR = 0.76, 95% confidence interval 0.63–0.92. This protective effect could not be attributed to confounding by other determinants. In analyses involving only the cases, NSAID exposure 2–5 and 6–10 years preceding diagnosis was associated with significantly reduced risks of presenting with a large tumour (> 5 cm diameter) or distant metastasis, but not regional lymph node metastasis. The use of NSAIDs may retard the growth of breast cancers and prevent distant metastasis. © 2000 Cancer Research Campaign
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spelling pubmed-23745292009-09-10 Nested case–control study of the effects of non-steroidal anti-inflammatory drugs on breast cancer risk and stage Sharpe, C R Collet, J-P McNutt, M Belzile, E Boivin, J-F Hanley, J A Br J Cancer Regular Article We carried out a nested case–control study to measure the rate ratio (RR) for invasive female breast cancer in relation to non-steroidal anti-inflammatory drug (NSAID) use. The source population consisted of the female beneficiaries of the Saskatchewan Prescription Drug Plan from 1981 to 1995 with no history of cancer since 1970. Four controls/case, matched on age and sampling time, were randomly selected. Dispensing rates during successive time periods characterized NSAID exposure. RRs associated with exposure during each period were adjusted for exposure during the others. Confounding by other determinants was studied in analyses adjusted with data obtained by interviewing samples of subjects accrued from mid-1991 to mid-1995. We accrued 5882 cases and 23 517 controls. Increasing NSAID exposure 2–5 years preceding diagnosis was associated with a trend towards a decreasing RR (P -trend = 0.003); for the highest exposure level RR = 0.76, 95% confidence interval 0.63–0.92. This protective effect could not be attributed to confounding by other determinants. In analyses involving only the cases, NSAID exposure 2–5 and 6–10 years preceding diagnosis was associated with significantly reduced risks of presenting with a large tumour (> 5 cm diameter) or distant metastasis, but not regional lymph node metastasis. The use of NSAIDs may retard the growth of breast cancers and prevent distant metastasis. © 2000 Cancer Research Campaign Nature Publishing Group 2000-07 2000-06-02 /pmc/articles/PMC2374529/ /pubmed/10883678 http://dx.doi.org/10.1054/bjoc.2000.1119 Text en Copyright © 2000 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
Sharpe, C R
Collet, J-P
McNutt, M
Belzile, E
Boivin, J-F
Hanley, J A
Nested case–control study of the effects of non-steroidal anti-inflammatory drugs on breast cancer risk and stage
title Nested case–control study of the effects of non-steroidal anti-inflammatory drugs on breast cancer risk and stage
title_full Nested case–control study of the effects of non-steroidal anti-inflammatory drugs on breast cancer risk and stage
title_fullStr Nested case–control study of the effects of non-steroidal anti-inflammatory drugs on breast cancer risk and stage
title_full_unstemmed Nested case–control study of the effects of non-steroidal anti-inflammatory drugs on breast cancer risk and stage
title_short Nested case–control study of the effects of non-steroidal anti-inflammatory drugs on breast cancer risk and stage
title_sort nested case–control study of the effects of non-steroidal anti-inflammatory drugs on breast cancer risk and stage
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2374529/
https://www.ncbi.nlm.nih.gov/pubmed/10883678
http://dx.doi.org/10.1054/bjoc.2000.1119
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