Triple-negative breast cancer is a clinically challenging disease, partly due to its molecular heterogeneity.1
Genomic profiling of cancer cells has revealed six distinct subtypes: Basal-like 1 (BL1), basal-like 2 (BL2), mesenchymal (M), mesenchymal stem-like (MSL), immunomodulatory (IM), and luminal androgen receptor (LAR).2
Basal-like breast cancers, which are intrinsically more aggressive forms of the disease, have the most substantial overlap with triple-negative breast cancer. BRCA1 mutations are frequent among patients with both of these cancer types.1
Dr Mark Harries, Consultant Medical Oncologist, Guy’s and St Thomas’ Hospitals Foundation Trust, summarises molecular subtypes and genomic pathway aberrations in triple-negative breast cancer.
(01:57 minutes)
References:
January 2024 UK-UNB-3381
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