Population-specific patterns in assessing molecular subtypes of young black females with triple-negative breast cancer

We determined triple-negative breast cancer (TNBC) subtypes, genetic ancestry, and immune features in a cohort of self-reported Black females with TNBC diagnosed at or below age 50. Among 104 tumors, 34.6% were basal-like 1 (BL1), 17.3% basal-like 2 (BL2), 9.6% luminal androgen receptor (LAR), 26.9% mesenchymal (M), and 11.5% unsubtyped (UNS). Subtypes resembled those seen in Europeans or East Asians, with less LAR (9.6% vs. 14.6-24.4%) and more UNS (11.5% vs. 0-7.5%). "High" proportion of West African ancestry was associated with more LAR (14.9% vs. 4.9%) and less M (25.5% vs. 34.2%). M demonstrated reduced immune activity and was marginally associated with worse overall survival in a multivariate model including stage, West African ancestry, BMI, and TILs, meriting future research. Our study is the largest to date of TNBC subtypes in young Black females. These results reinforce TNBC subtypes' application across populations and potential use as a prognostic biomarker.

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Publication Details

Journal
npj Breast Cancer
Published
2025-03-11
DOI
https://doi.org/10.1038/s41523-025-00731-0
Citations
3
Primary Topic
Cancer Immunotherapy and Biomarkers
Type
article
Field-Weighted Citation Impact
3.14

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article

Population-specific patterns in assessing molecular subtypes of young black females with triple-negative breast cancer

Melinda E. Sanders, Jibril Hirbo, Mya L. Roberson, Paula I. González-Ericsson et al.
3 citations
npj Breast Cancer
Cancer Immunotherapy and Biomarkers
3.14
article

Population-specific patterns in assessing molecular subtypes of young black females with triple-negative breast cancer

Melinda E. Sanders, Jibril Hirbo, Mya L. Roberson, Paula I. González-Ericsson, Anne Weidner, Susan T. Vadaparampil, Jennifer A. Pietenpol, Padma Sheila Rajagopal, Sonya Reid, Tuya Pal, Lindsay Venton, Marilin Rosa, Sean Yoder, Brian D. Lehmann, Jennifer G. Whisenant, Fei Ye, Xuefeng Wang, Run Fan
article en
3 citations

Abstract

We determined triple-negative breast cancer (TNBC) subtypes, genetic ancestry, and immune features in a cohort of self-reported Black females with TNBC diagnosed at or below age 50. Among 104 tumors, 34.6% were basal-like 1 (BL1), 17.3% basal-like 2 (BL2), 9.6% luminal androgen receptor (LAR), 26.9% mesenchymal (M), and 11.5% unsubtyped (UNS). Subtypes resembled those seen in Europeans or East Asians, with less LAR (9.6% vs. 14.6-24.4%) and more UNS (11.5% vs. 0-7.5%). "High" proportion of West African ancestry was associated with more LAR (14.9% vs. 4.9%) and less M (25.5% vs. 34.2%). M demonstrated reduced immune activity and was marginally associated with worse overall survival in a multivariate model including stage, West African ancestry, BMI, and TILs, meriting future research. Our study is the largest to date of TNBC subtypes in young Black females. These results reinforce TNBC subtypes' application across populations and potential use as a prognostic biomarker.

npj Breast CancerVol. 11(1)
University of North Carolina at Chapel Hill (US), University School of Nashville (US), Moffitt Cancer Center (US), National Cancer Institute (US), Center for Cancer Research (US), Vanderbilt University Medical Center (US)
American Association for Cancer Research, Susan G. Komen, National Cancer Institute
Good health and well-being
Openalex Percentile: Top 9%
Cancer Immunotherapy and Biomarkers
3.14
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