TY - JOUR
T1 - Oral Contraceptives and Breast Cancer Risk in the International BRCA1/2 Carrier Cohort Study
T2 - A report from EMBRACE, GENEPSO, GEO-HEBON, and the IBCCS Collaborating Group
AU - Brohet, Richard M.
AU - Goldgar, David E.
AU - Easton, Douglas F.
AU - Antoniou, Antonis C.
AU - Andrieu, Nadine
AU - Chang-Claude, Jenny
AU - Peock, Susan
AU - Eeles, Rosalind A.
AU - Cook, Margaret
AU - Chu, Carol
AU - Nogues, Catherine
AU - Lasset, Christine
AU - Berthet, Pascaline
AU - Meijers-Heijboer, Hanne
AU - Gerdes, Anne-Marie
AU - Olsson, Hakan
AU - Caldes, Trinidad
AU - van Leeuwen, Flora E.
AU - Rookus, Matti A.
AU - Gomez Garcia, Encarna B.
PY - 2007/9/1
Y1 - 2007/9/1
N2 - PurposeEarlier 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 MethodsIn 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.ResultsWe 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.
AB - PurposeEarlier 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 MethodsIn 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.ResultsWe 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.
KW - Ovarian-cancer
KW - Mutation carriers
KW - Noncarriers
KW - Women
KW - Oophorectomy
KW - History
KW - Series
U2 - 10.1200/JCO.2007.11.1179
DO - 10.1200/JCO.2007.11.1179
M3 - Article
C2 - 17635951
SN - 0732-183X
VL - 25
SP - 3831
EP - 3836
JO - Journal of Clinical Oncology
JF - Journal of Clinical Oncology
IS - 25
ER -