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

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作者
Francesco Schettini
Nuria Chic
Fara Brasó-Maristany
Laia Paré
Tomás Pascual
Benedetta Conte
Olga Martínez-Sáez
Barbara Adamo
Maria Vidal
Esther Barnadas
Aranzazu Fernández-Martinez
Blanca González-Farre
Esther Sanfeliu
Juan Miguel Cejalvo
Giuseppe Perrone
Giovanna Sabarese
Francesca Zalfa
Vicente Peg
Roberta Fasani
Patricia Villagrasa
Joaquín Gavilá
Carlos H. Barrios
Ana Lluch
Miguel Martín
Mariavittoria Locci
Sabino De Placido
Aleix Prat
机构
[1] University of Naples Federico II,Department of Clinical Medicine and Surgery
[2] Translational Genomics and Targeted Therapeutics in Solid Tumors,Department of Medical Oncology
[3] August Pi i Sunyer Biomedical Research Institute,Department of Genetics
[4] SOLTI Breast Cancer Research Group,Department of Medical Oncology, Ospedale Policlinico San Martino
[5] Hospital Clínic,Department of Pathology
[6] University of North Carolina,INCLIVA Biomedical Research Institute
[7] University of Genova,Pathology Department
[8] Hospital Clínic,Department of Neuroscience, Reproductive Sciences and Dentistry
[9] Hospital Clínico Universitario Valencia,undefined
[10] University of Valencia,undefined
[11] Campus Bio-Medico University,undefined
[12] Vall d´Hebron University Hospital,undefined
[13] GEICAM,undefined
[14] Grupo Español de Investigación en Cáncer de Mama,undefined
[15] Vall d’Hebron Institute of Oncology (VHIO),undefined
[16] Instituto Valenciano de Oncología (IVO),undefined
[17] Centro de Pesquisa Clínica Hospital São Lucas da PUCRS,undefined
[18] LACOG,undefined
[19] Latin American Cooperative Oncology Group,undefined
[20] Hospital Universitario Clínico Valencia,undefined
[21] Biomedical Research Centre Network in Cancer (CIBERONC),undefined
[22] Hospital Gregorio Marañon,undefined
[23] University of Naples Federico II,undefined
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摘要
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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