Race, Breast Cancer Subtypes, and Survival in the Carolina Breast Cancer Study
Top Cited Papers
- 7 June 2006
- journal article
- conference paper
- Published by American Medical Association (AMA) in JAMA
- Vol. 295 (21) , 2492-2502
- https://doi.org/10.1001/jama.295.21.2492
Abstract
Context Gene expression analysis has identified several breast cancer subtypes, including basal-like, human epidermal growth factor receptor-2 positive/estrogen receptor negative (HER2+/ER-), luminal A, and luminal B. Objectives To determine population-based distributions and clinical associations for breast cancer subtypes. Design, Setting, and Participants Immunohistochemical surrogates for each subtype were applied to 496 incident cases of invasive breast cancer from the Carolina Breast Cancer Study ( ascertained between May 1993 and December 1996), a population-based, case-control study that oversampled premenopausal and African American women. Subtype definitions were as follows: luminal A ( ER + and/or progesterone receptor positive [PR+], HER2-), luminal B ( ER + and/or PR +, HER2+), basal-like (ER-, PR-, HER2-, cytokeratin 5/6 positive, and/or HER1+), HER2+/ ER- ( ER-, PR-, and HER2+), and unclassified ( negative for all 5 markers). Main Outcome Measures We examined the prevalence of breast cancer subtypes within racial and menopausal subsets and determined their associations with tumor size, axillary nodal status, mitotic index, nuclear pleomorphism, combined grade, p53 mutation status, and breast cancer - specific survival. Results The basal-like breast cancer subtype was more prevalent among premenopausal African American women (39%) compared with postmenopausal African American women (14%) and non - African American women (16%) of any age ( P <. 001), whereas the luminal A subtype was less prevalent (36% vs 59% and 54%, respectively). The HER2+/ER-subtype did not vary with race or menopausal status (6%-9%). Compared with luminal A, basal-like tumors had more TP53 mutations (44% vs 15%, P <. 001), higher mitotic index ( odds ratio [ OR], 11.0; 95% confidence interval [CI], 5.6-21.7), more marked nuclear pleomorphism ( OR, 9.7; 95% CI, 5.3-18.0), and higher combined grade ( OR, 8.3; 95% CI, 4.4-15.6). Breast cancer - specific survival differed by subtype ( P <. 001), with shortest survival among HER2+/ER- and basal-like subtypes. Conclusions Basal-like breast tumors occurred at a higher prevalence among premenopausal African American patients compared with postmenopausal African American and non - African American patients in this population-based study. A higher prevalence of basal-like breast tumors and a lower prevalence of luminal A tumors could contribute to the poor prognosis of young African American women with breast cancer.Keywords
This publication has 10 references indexed in Scilit:
- Assessing genetic contributions to phenotypic differences among 'racial' and 'ethnic' groupsNature Genetics, 2004
- Will tomorrow's medicines work for everyone?Nature Genetics, 2004
- Mutation of GATA3 in human breast tumorsOncogene, 2004
- Racial differences in the expression of cell cycle–regulatory proteins in breast carcinomaCancer, 2004
- The logrank testBMJ, 2004
- Germline BRCA1 Mutations and a Basal Epithelial Phenotype in Breast CancerJNCI Journal of the National Cancer Institute, 2003
- Breast cancer classification and prognosis based on gene expression profiles from a population-based studyProceedings of the National Academy of Sciences, 2003
- Repeated observation of breast tumor subtypes in independent gene expression data setsProceedings of the National Academy of Sciences, 2003
- Racial differences in mammographic breast densityCancer, 2003
- Identification of Genes Periodically Expressed in the Human Cell Cycle and Their Expression in TumorsMolecular Biology of the Cell, 2002