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Oral contraceptives and breast cancer risk in the international BRCA1/2 carrier cohort study: A report from EMBRACE, GENEPSO, GEO-HEBON, and the IBCCS Collaborating Group

Brohet, Richard M. ; Goldgar, David E. ; Easton, Douglas F. ; Antoniou, Antonis C. ; Andrieu, Nadine ; Chang-Claude, Jenny ; Peock, Susan ; Eeles, Rosalind A. ; Cook, Margaret and Chu, Carol , et al. (2007) In Journal of Clinical Oncology 25(25). p.3831-3836
Abstract
Purpose Earlier studies have shown that endogenous gonadal hormones play an important role in the etiology of breast cancer among BRCA1/ 2 mutation carriers. So far, little is known about the safety of exogenous hormonal use in mutation carriers. In this study, we examined the association between oral contraceptive use and risk of breast cancer among BRCA1/ 2 carriers. Patients and Methods In the International BRCA1/ 2 Carrier Cohort study ( IBCCS), a retrospective cohort of 1,593 BRCA1/ 2 mutation carriers was analyzed with a weighted Cox regression analysis. Results We found an increased risk of breast cancer for BRCA1/ 2 mutation carriers who ever used oral contraceptives ( adjusted hazard ratio [ HR] = 1.47; 95% CI, 1.16 to 1.87). HRs... (More)
Purpose Earlier studies have shown that endogenous gonadal hormones play an important role in the etiology of breast cancer among BRCA1/ 2 mutation carriers. So far, little is known about the safety of exogenous hormonal use in mutation carriers. In this study, we examined the association between oral contraceptive use and risk of breast cancer among BRCA1/ 2 carriers. Patients and Methods In the International BRCA1/ 2 Carrier Cohort study ( IBCCS), a retrospective cohort of 1,593 BRCA1/ 2 mutation carriers was analyzed with a weighted Cox regression analysis. Results We found an increased risk of breast cancer for BRCA1/ 2 mutation carriers who ever used oral contraceptives ( adjusted hazard ratio [ HR] = 1.47; 95% CI, 1.16 to 1.87). HRs did not vary according to time since stopping use, age at start, or calendar year at start. However, a longer duration of use, especially before first full- term pregnancy, was associated with an increased risk of breast cancer for both BRCA1 and BRCA2 mutation carriers ( 4 or more years of use before first full-term pregnancy: HR = 1.49 [ 95% CI, 1.05 to 2.11] for BRCA1 carriers and HR = 2.58 [ 95% CI, 1.21 to 5.49] for BRCA2 carriers). Conclusion No evidence was found among BRCA1/ 2 mutation carriers that current use of oral contraceptives is associated with risk of breast cancer more strongly than is past use, as is found in the general population. However, duration of use, especially before first full- term pregnancy, may be associated with an increasing risk of breast cancer among both BRCA1 and BRCA2 mutation carriers. (Less)
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organization
publishing date
type
Contribution to journal
publication status
published
subject
keywords
Oral Contraceptives Breast Cancer International BRCA1/2 EMBRACE GENEPSO GEO-HEBON IBCCS
in
Journal of Clinical Oncology
volume
25
issue
25
pages
3831 - 3836
publisher
American Society of Clinical Oncology
external identifiers
  • wos:000249416000009
  • scopus:34548538897
  • pmid:17635951
ISSN
1527-7755
DOI
10.1200/JCO.2007.11.1179
language
English
LU publication?
yes
id
9cb45039-4e72-4793-8584-0a7fa98e0ad0 (old id 657236)
alternative location
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=17635951&dopt=Abstract
date added to LUP
2016-04-01 12:29:43
date last changed
2022-04-11 12:24:53
@article{9cb45039-4e72-4793-8584-0a7fa98e0ad0,
  abstract     = {{Purpose Earlier studies have shown that endogenous gonadal hormones play an important role in the etiology of breast cancer among BRCA1/ 2 mutation carriers. So far, little is known about the safety of exogenous hormonal use in mutation carriers. In this study, we examined the association between oral contraceptive use and risk of breast cancer among BRCA1/ 2 carriers. Patients and Methods In the International BRCA1/ 2 Carrier Cohort study ( IBCCS), a retrospective cohort of 1,593 BRCA1/ 2 mutation carriers was analyzed with a weighted Cox regression analysis. Results We found an increased risk of breast cancer for BRCA1/ 2 mutation carriers who ever used oral contraceptives ( adjusted hazard ratio [ HR] = 1.47; 95% CI, 1.16 to 1.87). HRs did not vary according to time since stopping use, age at start, or calendar year at start. However, a longer duration of use, especially before first full- term pregnancy, was associated with an increased risk of breast cancer for both BRCA1 and BRCA2 mutation carriers ( 4 or more years of use before first full-term pregnancy: HR = 1.49 [ 95% CI, 1.05 to 2.11] for BRCA1 carriers and HR = 2.58 [ 95% CI, 1.21 to 5.49] for BRCA2 carriers). Conclusion No evidence was found among BRCA1/ 2 mutation carriers that current use of oral contraceptives is associated with risk of breast cancer more strongly than is past use, as is found in the general population. However, duration of use, especially before first full- term pregnancy, may be associated with an increasing risk of breast cancer among both BRCA1 and BRCA2 mutation carriers.}},
  author       = {{Brohet, Richard M. and Goldgar, David E. and Easton, Douglas F. and Antoniou, Antonis C. and Andrieu, Nadine and Chang-Claude, Jenny and Peock, Susan and Eeles, Rosalind A. and Cook, Margaret and Chu, Carol and Nogues, Catherine and Lasset, Christine and Berthet, Pascaline and Meijers-Heijboer, Hanne and Gerdes, Anne-Marie and Olsson, Håkan and Caldes, Trinidad and van Leeuwen, Flora E. and Rookus, Matti A.}},
  issn         = {{1527-7755}},
  keywords     = {{Oral Contraceptives Breast Cancer International BRCA1/2 EMBRACE GENEPSO GEO-HEBON IBCCS}},
  language     = {{eng}},
  number       = {{25}},
  pages        = {{3831--3836}},
  publisher    = {{American Society of Clinical Oncology}},
  series       = {{Journal of Clinical Oncology}},
  title        = {{Oral contraceptives and breast cancer risk in the international BRCA1/2 carrier cohort study: A report from EMBRACE, GENEPSO, GEO-HEBON, and the IBCCS Collaborating Group}},
  url          = {{http://dx.doi.org/10.1200/JCO.2007.11.1179}},
  doi          = {{10.1200/JCO.2007.11.1179}},
  volume       = {{25}},
  year         = {{2007}},
}