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

Francesco Schettini(University of Naples Federico II), Núria Chic(Hospital Clínic de Barcelona), Fara Brasó‐Maristany(Hospital Clínic de Barcelona), Laia Paré, Tomás Pascual(University of North Carolina at Chapel Hill), Benedetta Conte(Ospedale Policlinico San Martino), Olga Martínez‐Sáez(Hospital Clínic de Barcelona), Bárbara Adamo(Hospital Clínic de Barcelona), María Vidal(Hospital Clínic de Barcelona), Esther Barnadas, Aranzazu Fernández-Martínez(University of North Carolina at Chapel Hill), Blanca González‐Farré(Hospital Clínic de Barcelona), Esther Sanfeliu(Hospital Clínic de Barcelona), Juan Miguel Cejalvo(Universitat de València), Giuseppe Perrone(Università Campus Bio-Medico), Giovanna Sabarese(Università Campus Bio-Medico), Francesca Zalfa(Università Campus Bio-Medico), Vicente Peg(Vall d'Hebron Hospital Universitari), Roberta Fasani(Vall d'Hebron Institute of Oncology), Patricia Villagrasa, Joaquín Gavilá(Fundación Instituto Valenciano de Oncología), Carlos H. Barrios(Hospital São Lucas da PUCRS), Aňa Lluch(Hospital Clínico Universitario de Valencia), Miguel Martín(Hospital General Universitario Gregorio Marañón), Mariavittoria Locci(University of Naples Federico II), Sabino De Placido(University of Naples Federico II), Aleix Prat(Breast Cancer Research Foundation)
npj Breast Cancer
January 4, 2021
Cited by 681Open Access
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Abstract

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.


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