Molecular subtypes of breast cancer in Jamaican women: high prevalence of triple-negative and HER2 + disease

Breast cancer incidence and mortality patterns vary significantly across populations, with women of African ancestry experiencing disproportionately higher mortality despite lower incidence rates. Jamaica reports concerning breast cancer mortality, yet comprehensive molecular characterization of breast cancer in this predominantly Black Caribbean population remains limited. We conducted a retrospective cross-sectional study of 1312 female breast cancer patients diagnosed at the University Hospital of the West Indies in Jamaica between January 2012 and December 2016. Medical records were reviewed for patient demographics, tumour characteristics, and receptor status (estrogen receptor, progesterone receptor, and HER2). Tumours were classified into four molecular subtypes: HR + /HER2- (estrogen receptor positive and/or progesterone receptor positive, HER2 negative), HR + /HER2 + (estrogen receptor positive and/or progesterone receptor positive, HER2 positive), HR-/HER2 + (estrogen receptor negative and progesterone receptor negative, HER2 positive), and triple-negative (HR-/HER2-: estrogen receptor negative and/ progesterone receptor negative, HER2 negative). Bivariate analyses and logistic regression models assessed associations between clinicopathological features and molecular subtypes. Mean age at diagnosis was 55.1 ± 13.6 years. The predominant tumour characteristics were invasive ductal histology (82%), SBR grade 2 (37%), and tumours ≤ 2 cm (31%). Molecular subtype distribution revealed HR + /HER2- (49%), HR + /HER2 + (13%), HR-/HER2 + (12%), and triple-negative (27%). Notably, total HER2 + disease accounted for 25% of cases. Triple-negative tumours were significantly associated higher grade (AOR = 13.92, p < 0.001), and smaller tumours had reduced odds of being triple negative (AOR = 0.47, p < 0.05). Lobular carcinomas showed lower odds of being triple-negative (AOR = 0.17, p < 0.01) compared to ductal carcinomas. Jamaican breast cancer patients exhibit a distinctive molecular profile with a high prevalence of both triple-negative (27%) and HER2 + (25%) disease, which likely contributes to poor outcomes in this population. These findings underscore the need for population-specific approaches to breast cancer management in Jamaica, including universal receptor testing and improved access to targeted therapies, particularly anti-HER2 agents.

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Journal
Breast Cancer Research
Published
2026-01-06
DOI
https://doi.org/10.1186/s13058-025-02175-7
Primary Topic
Breast Cancer Treatment Studies
Type
article
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article

Molecular subtypes of breast cancer in Jamaican women: high prevalence of triple-negative and HER2 + disease

Derria Cornwall, Richard Shaw, Patrick Roberts, Simone Badal et al.
Breast Cancer Research
Breast Cancer Treatment Studies
article

Molecular subtypes of breast cancer in Jamaican women: high prevalence of triple-negative and HER2 + disease

Derria Cornwall, Richard Shaw, Patrick Roberts, Simone Badal, Ayesha Johnson, Rory Thompson, Leo-Paul Powell
article en

Abstract

Breast cancer incidence and mortality patterns vary significantly across populations, with women of African ancestry experiencing disproportionately higher mortality despite lower incidence rates. Jamaica reports concerning breast cancer mortality, yet comprehensive molecular characterization of breast cancer in this predominantly Black Caribbean population remains limited. We conducted a retrospective cross-sectional study of 1312 female breast cancer patients diagnosed at the University Hospital of the West Indies in Jamaica between January 2012 and December 2016. Medical records were reviewed for patient demographics, tumour characteristics, and receptor status (estrogen receptor, progesterone receptor, and HER2). Tumours were classified into four molecular subtypes: HR + /HER2- (estrogen receptor positive and/or progesterone receptor positive, HER2 negative), HR + /HER2 + (estrogen receptor positive and/or progesterone receptor positive, HER2 positive), HR-/HER2 + (estrogen receptor negative and progesterone receptor negative, HER2 positive), and triple-negative (HR-/HER2-: estrogen receptor negative and/ progesterone receptor negative, HER2 negative). Bivariate analyses and logistic regression models assessed associations between clinicopathological features and molecular subtypes. Mean age at diagnosis was 55.1 ± 13.6 years. The predominant tumour characteristics were invasive ductal histology (82%), SBR grade 2 (37%), and tumours ≤ 2 cm (31%). Molecular subtype distribution revealed HR + /HER2- (49%), HR + /HER2 + (13%), HR-/HER2 + (12%), and triple-negative (27%). Notably, total HER2 + disease accounted for 25% of cases. Triple-negative tumours were significantly associated higher grade (AOR = 13.92, p < 0.001), and smaller tumours had reduced odds of being triple negative (AOR = 0.47, p < 0.05). Lobular carcinomas showed lower odds of being triple-negative (AOR = 0.17, p < 0.01) compared to ductal carcinomas. Jamaican breast cancer patients exhibit a distinctive molecular profile with a high prevalence of both triple-negative (27%) and HER2 + (25%) disease, which likely contributes to poor outcomes in this population. These findings underscore the need for population-specific approaches to breast cancer management in Jamaica, including universal receptor testing and improved access to targeted therapies, particularly anti-HER2 agents.

Breast Cancer ResearchVol. 28(1)
University of the West Indies System (JM), University of South Florida (US), University of the West Indies (JM)
Good health and well-being
Openalex Percentile: Top 96%
Breast Cancer Treatment Studies
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