Epidemiology of Basal-like and Luminal Breast Cancers among Black Women in the AMBER Consortium

Cancer Epidemiol Biomarkers Prev. 2021 Jan;30(1):71-79. doi: 10.1158/1055-9965.EPI-20-0556. Epub 2020 Oct 23.

Abstract

Background: Evidence suggests etiologic heterogeneity among breast cancer subtypes. Previous studies with six-marker IHC classification of intrinsic subtypes included small numbers of black women.

Methods: Using centralized laboratory results for estrogen receptor (ER), progesterone receptor, HER2, proliferation marker, Ki-67, EGFR, and cytokeratin (CK)5/6, we estimated case-only and case-control ORs for established breast cancer risk factors among cases (n = 2,354) and controls (n = 2,932) in the African American Breast Cancer Epidemiology and Risk (AMBER) consortium. ORs were estimated by ER status and intrinsic subtype using adjusted logistic regression.

Results: Case-only analyses by ER status showed etiologic heterogeneity by age at menarche, parity (vs. nulliparity), and age at first birth. In case-control analyses for intrinsic subtype, increased body mass index and waist-to-hip ratio (WHR) were associated with increased risk of luminal A subtype, whereas older age at menarche and parity, regardless of breastfeeding, were associated with reduced risk. For basal-like cancers, parity without breastfeeding and increasing WHR were associated with increased risk, whereas breastfeeding and age ≥25 years at first birth were associated with reduced risk among parous women. Basal-like and ER-/HER2+ subtypes had earlier age-at-incidence distribution relative to luminal subtypes.

Conclusions: Breast cancer subtypes showed distinct etiologic profiles in the AMBER consortium, a study of more than 5,000 black women with centrally assessed tumor biospecimens.

Impact: Among black women, high WHR and parity without breastfeeding are emerging as important intervention points to reduce the incidence of basal-like breast cancer.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Black or African American / statistics & numerical data
  • Breast Neoplasms / ethnology*
  • Breast Neoplasms / genetics
  • Female
  • Humans
  • Receptor, ErbB-2 / genetics*
  • Receptors, Estrogen / genetics*
  • Receptors, Progesterone / genetics*
  • Risk Factors
  • Triple Negative Breast Neoplasms / ethnology

Substances

  • Receptors, Estrogen
  • Receptors, Progesterone
  • Receptor, ErbB-2