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Clinical, pathological, and PAM50 gene expression features of HER2-low breast cancer.

Francesco SchettiniNuria ChicFara Brasó-MaristanyLaia ParéTomás PascualBenedetta ConteOlga Martínez-SáezBarbara AdamoMaría Jesús Vidal LosadaEsther BarnadasAranzazu Fernández-MartinezBlanca González-FarreEsther SanfeliuJuan Miguel CejalvoGiuseppe PerroneGiovanna SabareseFrancesca ZalfaVicente PegRoberta FasaniPatricia VillagrasaJoaquín GaviláCarlos Henrique BarriosAna LluchMiguel MartínMariavittoria LocciSabino De PlacidoAleix Prat
Published in: NPJ breast cancer (2021)
Novel antibody-drug conjugates against HER2 are showing high activity in HER2-negative breast cancer (BC) with low HER2 expression (i.e., 1+ or 2+ and lack of ERBB2 amplification). However, the clinical and molecular features of HER2-low BC are yet to be elucidated. Here, we collected retrospective clinicopathological and PAM50 data from 3,689 patients with HER2-negative disease and made the following observations. First, the proportion of HER2-low was higher in HR-positive disease (65.4%) than triple-negative BC (TNBC, 36.6%). Second, within HR-positive disease, ERBB2 and luminal-related genes were more expressed in HER2-low than HER2 0. In contrast, no gene was found differentially expressed in TNBC according to HER2 expression. Third, within HER2-low, ERBB2 levels were higher in HR-positive disease than TNBC. Fourth, HER2-low was not associated with overall survival in HR-positive disease and TNBC. Finally, the reproducibility of HER2-low among pathologists was suboptimal. This study emphasizes the large biological heterogeneity of HER2-low BC, and the need to implement reproducible and sensitive assays to measure low HER2 expression.
Keyphrases
  • gene expression
  • magnetic resonance
  • dna methylation
  • tyrosine kinase
  • single cell
  • genome wide
  • high throughput
  • cross sectional
  • transcription factor
  • binding protein