Breast cancer risk factors according to joint estrogen receptor and progesterone receptor status

Abstract

Background: We investigated risk factor patterns for subtypes of breast cancer characterized by joint estrogen receptor (ER) and progesterone receptor (PR) status in a hospital-based case-control study. Methods: ER and PR tumor status were determined immunohisotchemically. Risk factors of interest were entered into a multiple polychotomous logistic regression model simultaneously; odds ratios (ORs) and 95% confidence intervals (CIs) were calculated. Using this model, cases in the four tumor subtypes (ER +PR +, ER −PR −, ER +PR −, ER −PR +) were compared simultaneously to controls. A Wald test for heterogeneity across the four subtypes was conducted, as well as a case–case comparison between the two most biologically disparate subtypes, ER +PR + and ER −PR −. Results: The receptor status distribution was as follows: 33% ER +PR +, 34% ER −PR −, 20% ER +PR −, and 13% ER −PR +. Among 317 cases and 401 controls, we found significant heterogeneity across the four tumor subtypes for older age at first full-term pregnancy ( p = 0.04) and post-menopausal status ( p = 0.04). For older age at first full-term pregnancy, an elevated risk was found for the ER +PR − subtype (OR = 2.5; 95% CI: 1.2–5.1). For post-menopausal status, elevated risks were found for both the ER +PR + (OR = 2.4; 95% CI: 1.1–4.9) and ER +PR − (OR = 7.2; 95% CI: 2.4–21.7) subtypes. From the case–case comparisons, we found that cases, who had consumed alcohol for more than 1 year were 3.4 times more likely to have ER +PR + tumors than ER −PR − tumors (95% CI: 1.4–8.4). Conclusions: Certain breast cancer risk factors may vary by ER and PR status, and joint ER/PR status should be taken into account in future studies of risk factor estimates.