| Literature DB >> 33397968 |
Francesco Schettini1,2,3, Nuria Chic2,3,4, Fara Brasó-Maristany2,4, Laia Paré3, Tomás Pascual2,3,4,5, Benedetta Conte2,6, Olga Martínez-Sáez2,4, Barbara Adamo2,3,4, Maria Vidal2,3,4, Esther Barnadas2, Aranzazu Fernández-Martinez5, Blanca González-Farre2,3,7, Esther Sanfeliu2,3,7, Juan Miguel Cejalvo8, Giuseppe Perrone9, Giovanna Sabarese9, Francesca Zalfa9, Vicente Peg10,11, Roberta Fasani12, Patricia Villagrasa3, Joaquín Gavilá3,13, Carlos H Barrios14,15, Ana Lluch11,16,17, Miguel Martín11,18, Mariavittoria Locci19, Sabino De Placido1, Aleix Prat20,21,22.
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.Entities:
Year: 2021 PMID: 33397968 DOI: 10.1038/s41523-020-00208-2
Source DB: PubMed Journal: NPJ Breast Cancer ISSN: 2374-4677