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Regular use of aspirin and other non-steroidal anti-inflammatory drugs and breast cancer risk for women at familial or genetic risk: a cohort study

BACKGROUND: The use of aspirin and other non-steroidal anti-inflammatory drugs (NSAIDs) has been associated with reduced breast cancer risk, but it is not known if this association extends to women at familial or genetic risk. We examined the association between regular NSAID use and breast cancer r...

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Autores principales: Kehm, Rebecca D., Hopper, John L., John, Esther M., Phillips, Kelly-Anne, MacInnis, Robert J., Dite, Gillian S., Milne, Roger L., Liao, Yuyan, Zeinomar, Nur, Knight, Julia A., Southey, Melissa C., Vahdat, Linda, Kornhauser, Naomi, Cigler, Tessa, Chung, Wendy K., Giles, Graham G., McLachlan, Sue-Anne, Friedlander, Michael L., Weideman, Prue C., Glendon, Gord, Nesci, Stephanie, Andrulis, Irene L., Buys, Saundra S., Daly, Mary B., Terry, Mary Beth
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6471793/
https://www.ncbi.nlm.nih.gov/pubmed/30999962
http://dx.doi.org/10.1186/s13058-019-1135-y
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author Kehm, Rebecca D.
Hopper, John L.
John, Esther M.
Phillips, Kelly-Anne
MacInnis, Robert J.
Dite, Gillian S.
Milne, Roger L.
Liao, Yuyan
Zeinomar, Nur
Knight, Julia A.
Southey, Melissa C.
Vahdat, Linda
Kornhauser, Naomi
Cigler, Tessa
Chung, Wendy K.
Giles, Graham G.
McLachlan, Sue-Anne
Friedlander, Michael L.
Weideman, Prue C.
Glendon, Gord
Nesci, Stephanie
Andrulis, Irene L.
Buys, Saundra S.
Daly, Mary B.
Terry, Mary Beth
author_facet Kehm, Rebecca D.
Hopper, John L.
John, Esther M.
Phillips, Kelly-Anne
MacInnis, Robert J.
Dite, Gillian S.
Milne, Roger L.
Liao, Yuyan
Zeinomar, Nur
Knight, Julia A.
Southey, Melissa C.
Vahdat, Linda
Kornhauser, Naomi
Cigler, Tessa
Chung, Wendy K.
Giles, Graham G.
McLachlan, Sue-Anne
Friedlander, Michael L.
Weideman, Prue C.
Glendon, Gord
Nesci, Stephanie
Andrulis, Irene L.
Buys, Saundra S.
Daly, Mary B.
Terry, Mary Beth
author_sort Kehm, Rebecca D.
collection PubMed
description BACKGROUND: The use of aspirin and other non-steroidal anti-inflammatory drugs (NSAIDs) has been associated with reduced breast cancer risk, but it is not known if this association extends to women at familial or genetic risk. We examined the association between regular NSAID use and breast cancer risk using a large cohort of women selected for breast cancer family history, including 1054 BRCA1 or BRCA2 mutation carriers. METHODS: We analyzed a prospective cohort (N = 5606) and a larger combined, retrospective and prospective, cohort (N = 8233) of women who were aged 18 to 79 years, enrolled before June 30, 2011, with follow-up questionnaire data on medication history. The prospective cohort was further restricted to women without breast cancer when medication history was asked by questionnaire. Women were recruited from seven study centers in the United States, Canada, and Australia. Associations were estimated using multivariable Cox proportional hazards regression models adjusted for demographics, lifestyle factors, family history, and other medication use. Women were classified as regular or non-regular users of aspirin, COX-2 inhibitors, ibuprofen and other NSAIDs, and acetaminophen (control) based on self-report at follow-up of ever using the medication for at least twice a week for ≥1 month prior to breast cancer diagnosis. The main outcome was incident invasive breast cancer, based on self- or relative-report (81% confirmed pathologically). RESULTS: From fully adjusted analyses, regular aspirin use was associated with a 39% and 37% reduced risk of breast cancer in the prospective (HR = 0.61; 95% CI = 0.33–1.14) and combined cohorts (HR = 0.63; 95% CI = 0.57–0.71), respectively. Regular use of COX-2 inhibitors was associated with a 61% and 71% reduced risk of breast cancer (prospective HR = 0.39; 95% CI = 0.15–0.97; combined HR = 0.29; 95% CI = 0.23–0.38). Other NSAIDs and acetaminophen were not associated with breast cancer risk in either cohort. Associations were not modified by familial risk, and consistent patterns were found by BRCA1 and BRCA2 carrier status, estrogen receptor status, and attained age. CONCLUSION: Regular use of aspirin and COX-2 inhibitors might reduce breast cancer risk for women at familial or genetic risk. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13058-019-1135-y) contains supplementary material, which is available to authorized users.
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spelling pubmed-64717932019-04-24 Regular use of aspirin and other non-steroidal anti-inflammatory drugs and breast cancer risk for women at familial or genetic risk: a cohort study Kehm, Rebecca D. Hopper, John L. John, Esther M. Phillips, Kelly-Anne MacInnis, Robert J. Dite, Gillian S. Milne, Roger L. Liao, Yuyan Zeinomar, Nur Knight, Julia A. Southey, Melissa C. Vahdat, Linda Kornhauser, Naomi Cigler, Tessa Chung, Wendy K. Giles, Graham G. McLachlan, Sue-Anne Friedlander, Michael L. Weideman, Prue C. Glendon, Gord Nesci, Stephanie Andrulis, Irene L. Buys, Saundra S. Daly, Mary B. Terry, Mary Beth Breast Cancer Res Research Article BACKGROUND: The use of aspirin and other non-steroidal anti-inflammatory drugs (NSAIDs) has been associated with reduced breast cancer risk, but it is not known if this association extends to women at familial or genetic risk. We examined the association between regular NSAID use and breast cancer risk using a large cohort of women selected for breast cancer family history, including 1054 BRCA1 or BRCA2 mutation carriers. METHODS: We analyzed a prospective cohort (N = 5606) and a larger combined, retrospective and prospective, cohort (N = 8233) of women who were aged 18 to 79 years, enrolled before June 30, 2011, with follow-up questionnaire data on medication history. The prospective cohort was further restricted to women without breast cancer when medication history was asked by questionnaire. Women were recruited from seven study centers in the United States, Canada, and Australia. Associations were estimated using multivariable Cox proportional hazards regression models adjusted for demographics, lifestyle factors, family history, and other medication use. Women were classified as regular or non-regular users of aspirin, COX-2 inhibitors, ibuprofen and other NSAIDs, and acetaminophen (control) based on self-report at follow-up of ever using the medication for at least twice a week for ≥1 month prior to breast cancer diagnosis. The main outcome was incident invasive breast cancer, based on self- or relative-report (81% confirmed pathologically). RESULTS: From fully adjusted analyses, regular aspirin use was associated with a 39% and 37% reduced risk of breast cancer in the prospective (HR = 0.61; 95% CI = 0.33–1.14) and combined cohorts (HR = 0.63; 95% CI = 0.57–0.71), respectively. Regular use of COX-2 inhibitors was associated with a 61% and 71% reduced risk of breast cancer (prospective HR = 0.39; 95% CI = 0.15–0.97; combined HR = 0.29; 95% CI = 0.23–0.38). Other NSAIDs and acetaminophen were not associated with breast cancer risk in either cohort. Associations were not modified by familial risk, and consistent patterns were found by BRCA1 and BRCA2 carrier status, estrogen receptor status, and attained age. CONCLUSION: Regular use of aspirin and COX-2 inhibitors might reduce breast cancer risk for women at familial or genetic risk. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13058-019-1135-y) contains supplementary material, which is available to authorized users. BioMed Central 2019-04-18 2019 /pmc/articles/PMC6471793/ /pubmed/30999962 http://dx.doi.org/10.1186/s13058-019-1135-y Text en © The Author(s). 2019 Open AccessThis 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 Research Article
Kehm, Rebecca D.
Hopper, John L.
John, Esther M.
Phillips, Kelly-Anne
MacInnis, Robert J.
Dite, Gillian S.
Milne, Roger L.
Liao, Yuyan
Zeinomar, Nur
Knight, Julia A.
Southey, Melissa C.
Vahdat, Linda
Kornhauser, Naomi
Cigler, Tessa
Chung, Wendy K.
Giles, Graham G.
McLachlan, Sue-Anne
Friedlander, Michael L.
Weideman, Prue C.
Glendon, Gord
Nesci, Stephanie
Andrulis, Irene L.
Buys, Saundra S.
Daly, Mary B.
Terry, Mary Beth
Regular use of aspirin and other non-steroidal anti-inflammatory drugs and breast cancer risk for women at familial or genetic risk: a cohort study
title Regular use of aspirin and other non-steroidal anti-inflammatory drugs and breast cancer risk for women at familial or genetic risk: a cohort study
title_full Regular use of aspirin and other non-steroidal anti-inflammatory drugs and breast cancer risk for women at familial or genetic risk: a cohort study
title_fullStr Regular use of aspirin and other non-steroidal anti-inflammatory drugs and breast cancer risk for women at familial or genetic risk: a cohort study
title_full_unstemmed Regular use of aspirin and other non-steroidal anti-inflammatory drugs and breast cancer risk for women at familial or genetic risk: a cohort study
title_short Regular use of aspirin and other non-steroidal anti-inflammatory drugs and breast cancer risk for women at familial or genetic risk: a cohort study
title_sort regular use of aspirin and other non-steroidal anti-inflammatory drugs and breast cancer risk for women at familial or genetic risk: a cohort study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6471793/
https://www.ncbi.nlm.nih.gov/pubmed/30999962
http://dx.doi.org/10.1186/s13058-019-1135-y
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