Oral contraceptive use and risk of early-onset breast cancer in carriers and noncarriers of BRCA1 and BRCA2 mutations

被引:95
作者
Milne, RL
Knight, JA
John, EM
Dite, GS
Balbuena, R
Ziogas, A
Andrulis, IL
West, DW
Li, FP
Southey, MC
Giles, GG
McCredie, MRE
Hopper, JL
Whittemore, AS
机构
[1] Univ Melbourne, Ctr Genet Epidemiol, Melbourne, Vic 3053, Australia
[2] Univ Melbourne, Dept Pathol, Melbourne, Vic 3053, Australia
[3] Canc Council Victoria, Canc Epidemiol Ctr, Carlton, Vic, Australia
[4] Univ Otago, Dept Social & Prevent Med, Dunedin, New Zealand
[5] Mt Sinai Hosp, Samuel Lunenfeld Res Inst, Toronto, ON M5G 1X5, Canada
[6] Canc Care Ontario, Toronto, ON, Canada
[7] Univ Calif Irvine, Dept Med, Div Epidemiol, Irvine, CA 92717 USA
[8] No Calif Canc Ctr, Union City, CA USA
[9] Stanford Univ, Dept Hlth Res & Policy, Stanford, CA 94305 USA
[10] Dana Farber Canc Inst, Boston, MA 02115 USA
关键词
D O I
10.1158/1055-9965.EPI-04-0376
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Recent oral contraceptive use has been associated with a small increase in breast cancer risk and a substantial decrease in ovarian cancer risk. The effects on risks for women with germ line mutations in BRCA1 or BRCA2 are unclear. Methods: Subjects were population-based samples of Caucasian women that comprised 1,156 incident cases of invasive breast cancer diagnosed before age 40 (including 47 BRCA1 and 36 BRCA2 mutation carriers) and 815 controls from the San Francisco Bay area, California, Ontario, Canada, and Melbourne and Sydney, Australia. Relative risks by carrier status were estimated using unconditional logistic regression, comparing oral contraceptive use in case groups defined by mutation status with that in controls. Results: After adjustment for potential confounders, oral contraceptive use for at least 12 months was associated with decreased breast cancer risk for BRCA1 mutation carriers [odds ratio (OR), 0.22; 95% confidence interval (CI), 0.10-0.49; P < 0.001], but not for BRCA2 mutation carriers (OR, 1.02; 95% Cl, 0.34-3.09) or noncarriers (OR, 0.93; 95% Cl, 0.69-1.24). First use during or before 1975 was associated with increased risk for noncarriers (OR, 1.52 per year of use before 1976; 95% CI, 1.22-1.91; P < 0.001). Conclusions: There was no evidence that use of current low-dose oral contraceptive formulations increases risk of early-onset breast cancer for mutation carriers, and there may be a reduced risk for BRCA1 mutation carriers. Because current formulations of oral contraceptives may reduce, or at least not exacerbate, ovarian cancer risk for mutation carriers, they should not be contraindicated for a woman with a germ line mutation in BRCA1 or BRCA2.
引用
收藏
页码:350 / 356
页数:7
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