Standard Clinical Assays Obscure Breast Cancer Subtype Diversity

The same tumors were also tested for their molecular features and classified into one of five molecular subtypes: Luminal A, Luminal B, HER2-Enriched, Basal-like, and Normal-like.

These breast tumors were centrally reviewed in three different trials for quantitative ER, PR, and HER2 expression by immunohistochemistry (IHC) stain and by reverse transcription-quantitative polymerase chain reaction (RT-qPCR), with intrinsic subtyping by the gene set PAM50 RT-qPCR assay. HER2 expression was determined by IHC, and the amplification ratio was determined by fluorescent in situ hybridization (FISH) and also by chromogenic in situ hybridization (CISH).

Among TNBCs with less than 1% hormone receptor (HR) staining, the most common molecular subtype was Basal-like (73%), followed by HER2-Enriched (17%). By comparison, TNBC tumors with borderline HR staining had a much wider mix of molecular subtypes, including Luminal A/B (44%), HER2-Enriched (31%), and Basal-like (18%). Among the 228 basal-like tumors, 93.4% (213 of 228) had less than 1% ER or PR staining by IHC.

Lisa A. Carey, MD, the senior author of the study, said, “Including tumors with borderline HR staining in the definition of triple-negative breast cancer significantly diminished the proportion of Basal-like molecular subtypes. The optimal threshold for enriching for Basal-like breast cancer is less than 1% for either hormone receptor. Our findings show that borderline HR-expressing tumors are heterogeneous and do not fit well into distinct molecular categories. This raises the question of whether ‘borderline’ HR staining should instead be considered ‘indeterminate’ and requires additional assays to clarify the underlying biology.” The study was published on April 23, 2015, in the journal the Oncologist.

Related Links:
University of North Carolina