Risk factors for breast cancer according to estrogen and progesterone receptor status
- PMID: 14759989
- DOI: 10.1093/jnci/djh025
Risk factors for breast cancer according to estrogen and progesterone receptor status
Abstract
Background: Evaluations of epidemiologic risk factors in relation to breast cancer classified jointly by estrogen receptor (ER) and progesterone receptor (PR) status have been inconsistent. To address this issue, we conducted a prospective evaluation of risk factors for breast cancer classified according to receptor status.
Methods: During 1 029 414 person-years of follow-up of 66 145 women participating in the Nurses' Health Study from 1980 through 2000, we identified 2096 incident cases of breast cancer for which information on ER/PR status was available: 1281 were ER+/PR+, 318 were ER+/PR-, 80 were ER-/PR+, and 417 were ER-/PR-. We fit a log-incidence model of breast cancer and used polychotomous logistic regression to compare coefficients for breast cancer risk factors in patients with different ER/PR status. To test for differences in risk factor odds ratios based on marginal ER/PR categories, we evaluated ER status controlling for PR status and vice versa. The predictive ability of our log-incidence model to discriminate between women who would develop ER+/PR+ breast cancer and those who would not (and similarly for ER-/PR- breast cancer) was evaluated by using receiver operator characteristic curve analysis. All statistical tests were two-sided.
Results: We observed statistically significant heterogeneity among the four ER/PR categories for some risk factors (age, menopausal status, body mass index [BMI] after menopause, the one-time adverse effect of first pregnancy, and past use of postmenopausal hormones) but not for others (benign breast disease, family history of breast cancer, alcohol use, and height). The one-time adverse association of first pregnancy with incidence was present for PR- but not for PR+ tumors after controlling for ER status (P =.007). However, the association of BMI after menopause with incidence was present for PR+ but not PR- tumors (P =.005). Statistically significant differences in the incidence of ER+ and ER- tumors were seen with age, both before and after menopause (P =.003), and with past use of postmenopausal hormones (P =.01). Area under the receiver operator characteristic curve, adjusted for age, was 0.64 (95% confidence interval [CI] = 0.63 to 0.66) for ER+/PR+ tumors and 0.61 (95% CI = 0.58 to 0.64) for ER-/PR- tumors.
Conclusions: Incidence rates and risk factors for breast cancer differ according to ER and PR status. Thus, to accurately estimate breast cancer risk, breast cancer cases should be divided according to the ER and PR status of the tumor.
Similar articles
-
Alcohol and postmenopausal breast cancer risk defined by estrogen and progesterone receptor status: a prospective cohort study.J Natl Cancer Inst. 2005 Nov 2;97(21):1601-8. doi: 10.1093/jnci/dji341. J Natl Cancer Inst. 2005. PMID: 16264180
-
Association between family history of cancer and breast cancer defined by estrogen and progesterone receptor status.Genet Epidemiol. 1996;13(2):207-21. doi: 10.1002/(SICI)1098-2272(1996)13:2<207::AID-GEPI6>3.0.CO;2-4. Genet Epidemiol. 1996. PMID: 8722747 Clinical Trial.
-
Predicting risk of breast cancer in postmenopausal women by hormone receptor status.J Natl Cancer Inst. 2007 Nov 21;99(22):1695-705. doi: 10.1093/jnci/djm224. Epub 2007 Nov 13. J Natl Cancer Inst. 2007. PMID: 18000216
-
Adult weight gain in relation to breast cancer risk by estrogen and progesterone receptor status: a meta-analysis.Breast Cancer Res Treat. 2010 Oct;123(3):641-9. doi: 10.1007/s10549-010-1116-4. Epub 2010 Aug 15. Breast Cancer Res Treat. 2010. PMID: 20711809 Review.
-
90 YEARS OF PROGESTERONE: Progesterone and progesterone receptors in breast cancer: past, present, future.J Mol Endocrinol. 2020 Jul;65(1):T49-T63. doi: 10.1530/JME-20-0104. J Mol Endocrinol. 2020. PMID: 32485679 Free PMC article. Review.
Cited by
-
Progesterone receptor loss identifies hormone receptor-positive and HER2-negative breast cancer subgroups at higher risk of relapse: a retrospective cohort study.Onco Targets Ther. 2016 Mar 21;9:1707-13. doi: 10.2147/OTT.S98666. eCollection 2016. Onco Targets Ther. 2016. PMID: 27051305 Free PMC article.
-
Alcohol consumption before and after breast cancer diagnosis: associations with survival from breast cancer, cardiovascular disease, and other causes.J Clin Oncol. 2013 Jun 1;31(16):1939-46. doi: 10.1200/JCO.2012.46.5765. Epub 2013 Apr 8. J Clin Oncol. 2013. PMID: 23569314 Free PMC article.
-
Low-Grade Inflammation, Oxidative Stress and Risk of Invasive Post-Menopausal Breast Cancer - A Nested Case-Control Study from the Malmö Diet and Cancer Cohort.PLoS One. 2016 Jul 8;11(7):e0158959. doi: 10.1371/journal.pone.0158959. eCollection 2016. PLoS One. 2016. PMID: 27391324 Free PMC article. Clinical Trial.
-
FGFR2 gene polymorphisms are associated with breast cancer risk in the Han Chinese population.Am J Cancer Res. 2015 Apr 15;5(5):1854-61. eCollection 2015. Am J Cancer Res. 2015. PMID: 26175953 Free PMC article.
-
Evidence for Etiologic Subtypes of Breast Cancer in the Carolina Breast Cancer Study.Cancer Epidemiol Biomarkers Prev. 2019 Nov;28(11):1784-1791. doi: 10.1158/1055-9965.EPI-19-0365. Epub 2019 Aug 8. Cancer Epidemiol Biomarkers Prev. 2019. PMID: 31395590 Free PMC article.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Research Materials
Miscellaneous