A case-control analysis of oral contraceptive use and breast cancer subtypes in the African American Breast Cancer Epidemiology and Risk Consortium

被引:35
|
作者
Bethea, Traci N. [1 ]
Rosenberg, Lynn [1 ]
Hong, Chi-Chen [2 ]
Troester, Melissa A. [3 ]
Lunetta, Kathryn L. [4 ]
Bandera, Elisa V. [5 ]
Schedin, Pepper [6 ]
Kolonel, Laurence N. [7 ]
Olshan, Andrew F. [3 ]
Ambrosone, Christine B. [2 ]
Palmer, Julie R. [1 ]
机构
[1] Boston Univ, Slone Epidemiol Ctr, Boston, MA 02215 USA
[2] Roswell Pk Canc Inst, Dept Canc Prevent & Control, Buffalo, NY 14263 USA
[3] Univ N Carolina, Dept Epidemiol, Chapel Hill, NC 27599 USA
[4] Boston Univ, Sch Publ Hlth, Dept Biostat, Boston, MA 02118 USA
[5] Rutgers State Univ, Rutgers Canc Inst New Jersey, Canc Prevent & Control Program, New Brunswick, NJ 08903 USA
[6] Oregon Hlth & Sci Univ, Dept Cell Dev & Canc Biol, Portland, OR 97239 USA
[7] Univ Hawaii, Ctr Canc, Canc Epidemiol Program, Honolulu, HI 96813 USA
关键词
TRIPLE-NEGATIVE PHENOTYPE; ESTROGEN-RECEPTOR; PREMENOPAUSAL WOMEN; DNA METHYLATION; WHITE WOMEN; BODY-SIZE; AGE; ASSOCIATION; BLACK; FORMULATION;
D O I
10.1186/s13058-015-0535-x
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction: Recent oral contraceptive (OC) use has been consistently associated with increased risk of breast cancer, but evidence on specific breast cancer subtypes is sparse. Methods: We investigated recency and duration of OC use in relation to molecular subtypes of breast cancer in a pooled analysis of data from the African American Breast Cancer Epidemiology and Risk Consortium. The study included 1,848 women with estrogen receptor-positive (ER+) breast cancer, 1,043 with ER-negative (ER-) breast cancer (including 494 triple negative (TN) tumors, which do not have receptors for estrogen, progesterone, and human epidermal growth factor 2), and 10,044 controls. Multivariable polytomous logistic regression models were used to estimate odds ratios (ORs) and 95% confidence intervals (CIs) for exposure categories relative to never use, controlling for potential confounding variables. Results: OC use within the previous 5 years was associated with increased risk of ER+ (OR 1.46, 95% CI 1.18 to 1.81), ER-(OR 1.57, 95% CI 1.22 to 1.43), and TN (OR 1.78, 95% CI 1.25 to 2.53) breast cancer. The risk declined after cessation of use but was apparent for ER+ cancer for 15 to 19 years after cessation and for ER-breast cancer for an even longer interval after cessation. Long duration of use was also associated with increased risk of each subtype, particularly ER-. Conclusions: Our results suggest that OC use, particularly recent use of long duration, is associated with an increased risk of ER+, ER-, and TN breast cancer in African American women. Research into mechanisms that explain these findings, especially the association with ER-breast cancer, is needed.
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页数:13
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