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Oral Contraceptive Use in BRCA1 and BRCA2 Mutation Carriers: Absolute Cancer Risks and Benefits
BACKGROUND: To help BRCA1 and 2 mutation carriers make informed decisions regarding use of combined-type oral contraceptive preparation (COCP), absolute risk-benefit estimates are needed for COCP-associated cancer. METHODS: For a hypothetical cohort of 10 000 women, we calculated the increased or de...
Autores principales: | , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9002279/ https://www.ncbi.nlm.nih.gov/pubmed/35048954 http://dx.doi.org/10.1093/jnci/djac004 |
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author | Schrijver, Lieske H Mooij, Thea M Pijpe, Anouk Sonke, Gabe S Mourits, Marian J E Andrieu, Nadine Antoniou, Antonis C Easton, Douglas F Engel, Christoph Goldgar, David John, Esther M Kast, Karin Milne, Roger L Olsson, Håkan Phillips, Kelly-Anne Terry, Mary Beth Hopper, John L van Leeuwen, Flora E Rookus, Matti A |
author_facet | Schrijver, Lieske H Mooij, Thea M Pijpe, Anouk Sonke, Gabe S Mourits, Marian J E Andrieu, Nadine Antoniou, Antonis C Easton, Douglas F Engel, Christoph Goldgar, David John, Esther M Kast, Karin Milne, Roger L Olsson, Håkan Phillips, Kelly-Anne Terry, Mary Beth Hopper, John L van Leeuwen, Flora E Rookus, Matti A |
author_sort | Schrijver, Lieske H |
collection | PubMed |
description | BACKGROUND: To help BRCA1 and 2 mutation carriers make informed decisions regarding use of combined-type oral contraceptive preparation (COCP), absolute risk-benefit estimates are needed for COCP-associated cancer. METHODS: For a hypothetical cohort of 10 000 women, we calculated the increased or decreased cumulative incidence of COCP-associated (breast, ovarian, endometrial) cancer, examining 18 scenarios with differences in duration and timing of COCP use, uptake of prophylactic surgeries, and menopausal hormone therapy. RESULTS: COCP use initially increased breast cancer risk and decreased ovarian and endometrial cancer risk long term. For 10 000 BRCA1 mutation carriers, 10 years of COCP use from age 20 to 30 years resulted in 66 additional COCP-associated cancer cases by the age of 35 years, in addition to 625 cases expected for never users. By the age of 70 years such COCP use resulted in 907 fewer cancer cases than the expected 9093 cases in never users. Triple-negative breast cancer estimates resulted in 196 additional COCP-associated cases by age 40 years, in addition to the 1454 expected. For 10 000 BRCA2 mutation carriers using COCP from age 20 to 30 years, 80 excess cancer cases were estimated by age 40 years in addition to 651 expected cases; by the age of 70 years, we calculated 382 fewer cases compared with the 6156 cases expected. The long-term benefit of COCP use diminished after risk-reducing bilateral salpingo-oophorectomy followed by menopausal hormone therapy use. CONCLUSION: Although COCP use in BRCA1 and BRCA2 mutation carriers initially increases breast, ovarian, and endometrial cancer risk, it strongly decreases lifetime cancer risk. Risk-reducing bilateral salpingo-oophorectomy and menopausal hormone therapy use appear to counteract the long-term COCP-benefit. |
format | Online Article Text |
id | pubmed-9002279 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-90022792022-04-12 Oral Contraceptive Use in BRCA1 and BRCA2 Mutation Carriers: Absolute Cancer Risks and Benefits Schrijver, Lieske H Mooij, Thea M Pijpe, Anouk Sonke, Gabe S Mourits, Marian J E Andrieu, Nadine Antoniou, Antonis C Easton, Douglas F Engel, Christoph Goldgar, David John, Esther M Kast, Karin Milne, Roger L Olsson, Håkan Phillips, Kelly-Anne Terry, Mary Beth Hopper, John L van Leeuwen, Flora E Rookus, Matti A J Natl Cancer Inst Articles BACKGROUND: To help BRCA1 and 2 mutation carriers make informed decisions regarding use of combined-type oral contraceptive preparation (COCP), absolute risk-benefit estimates are needed for COCP-associated cancer. METHODS: For a hypothetical cohort of 10 000 women, we calculated the increased or decreased cumulative incidence of COCP-associated (breast, ovarian, endometrial) cancer, examining 18 scenarios with differences in duration and timing of COCP use, uptake of prophylactic surgeries, and menopausal hormone therapy. RESULTS: COCP use initially increased breast cancer risk and decreased ovarian and endometrial cancer risk long term. For 10 000 BRCA1 mutation carriers, 10 years of COCP use from age 20 to 30 years resulted in 66 additional COCP-associated cancer cases by the age of 35 years, in addition to 625 cases expected for never users. By the age of 70 years such COCP use resulted in 907 fewer cancer cases than the expected 9093 cases in never users. Triple-negative breast cancer estimates resulted in 196 additional COCP-associated cases by age 40 years, in addition to the 1454 expected. For 10 000 BRCA2 mutation carriers using COCP from age 20 to 30 years, 80 excess cancer cases were estimated by age 40 years in addition to 651 expected cases; by the age of 70 years, we calculated 382 fewer cases compared with the 6156 cases expected. The long-term benefit of COCP use diminished after risk-reducing bilateral salpingo-oophorectomy followed by menopausal hormone therapy use. CONCLUSION: Although COCP use in BRCA1 and BRCA2 mutation carriers initially increases breast, ovarian, and endometrial cancer risk, it strongly decreases lifetime cancer risk. Risk-reducing bilateral salpingo-oophorectomy and menopausal hormone therapy use appear to counteract the long-term COCP-benefit. Oxford University Press 2022-01-20 /pmc/articles/PMC9002279/ /pubmed/35048954 http://dx.doi.org/10.1093/jnci/djac004 Text en © The Author(s) 2022. Published by Oxford University Press. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Articles Schrijver, Lieske H Mooij, Thea M Pijpe, Anouk Sonke, Gabe S Mourits, Marian J E Andrieu, Nadine Antoniou, Antonis C Easton, Douglas F Engel, Christoph Goldgar, David John, Esther M Kast, Karin Milne, Roger L Olsson, Håkan Phillips, Kelly-Anne Terry, Mary Beth Hopper, John L van Leeuwen, Flora E Rookus, Matti A Oral Contraceptive Use in BRCA1 and BRCA2 Mutation Carriers: Absolute Cancer Risks and Benefits |
title | Oral Contraceptive Use in BRCA1 and BRCA2
Mutation Carriers: Absolute Cancer Risks and Benefits |
title_full | Oral Contraceptive Use in BRCA1 and BRCA2
Mutation Carriers: Absolute Cancer Risks and Benefits |
title_fullStr | Oral Contraceptive Use in BRCA1 and BRCA2
Mutation Carriers: Absolute Cancer Risks and Benefits |
title_full_unstemmed | Oral Contraceptive Use in BRCA1 and BRCA2
Mutation Carriers: Absolute Cancer Risks and Benefits |
title_short | Oral Contraceptive Use in BRCA1 and BRCA2
Mutation Carriers: Absolute Cancer Risks and Benefits |
title_sort | oral contraceptive use in brca1 and brca2
mutation carriers: absolute cancer risks and benefits |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9002279/ https://www.ncbi.nlm.nih.gov/pubmed/35048954 http://dx.doi.org/10.1093/jnci/djac004 |
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