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Clinical, pathological, and PAM50 gene expression features of HER2-low breast cancer.
Schettini, Francesco; Chic, Nuria; Brasó-Maristany, Fara; Paré, Laia; Pascual, Tomás; Conte, Benedetta; Martínez-Sáez, Olga; Adamo, Barbara; Vidal, Maria; Barnadas, Esther; Fernández-Martinez, Aranzazu; González-Farre, Blanca; Sanfeliu, Esther; Cejalvo, Juan Miguel; Perrone, Giuseppe; Sabarese, Giovanna; Zalfa, Francesca; Peg, Vicente; Fasani, Roberta; Villagrasa, Patricia; Gavilá, Joaquín; Barrios, Carlos H; Lluch, Ana; Martín, Miguel; Locci, Mariavittoria; De Placido, Sabino; Prat, Aleix.
Affiliation
  • Schettini F; Department of Clinical Medicine and Surgery, University of Naples Federico II, Naples, Italy.
  • Chic N; Translational Genomics and Targeted Therapeutics in Solid Tumors, August Pi i Sunyer Biomedical Research Institute, Barcelona, Spain.
  • Brasó-Maristany F; SOLTI Breast Cancer Research Group, Barcelona, Spain.
  • Paré L; Translational Genomics and Targeted Therapeutics in Solid Tumors, August Pi i Sunyer Biomedical Research Institute, Barcelona, Spain.
  • Pascual T; SOLTI Breast Cancer Research Group, Barcelona, Spain.
  • Conte B; Department of Medical Oncology, Hospital Clínic, Barcelona, Spain.
  • Martínez-Sáez O; Translational Genomics and Targeted Therapeutics in Solid Tumors, August Pi i Sunyer Biomedical Research Institute, Barcelona, Spain.
  • Adamo B; Department of Medical Oncology, Hospital Clínic, Barcelona, Spain.
  • Vidal M; SOLTI Breast Cancer Research Group, Barcelona, Spain.
  • Barnadas E; Translational Genomics and Targeted Therapeutics in Solid Tumors, August Pi i Sunyer Biomedical Research Institute, Barcelona, Spain.
  • Fernández-Martinez A; SOLTI Breast Cancer Research Group, Barcelona, Spain.
  • González-Farre B; Department of Medical Oncology, Hospital Clínic, Barcelona, Spain.
  • Sanfeliu E; Department of Genetics, University of North Carolina, Chapel Hill, NC, USA.
  • Cejalvo JM; Translational Genomics and Targeted Therapeutics in Solid Tumors, August Pi i Sunyer Biomedical Research Institute, Barcelona, Spain.
  • Perrone G; Department of Medical Oncology, Ospedale Policlinico San Martino, University of Genova, Genova, Italy.
  • Sabarese G; Translational Genomics and Targeted Therapeutics in Solid Tumors, August Pi i Sunyer Biomedical Research Institute, Barcelona, Spain.
  • Zalfa F; Department of Medical Oncology, Hospital Clínic, Barcelona, Spain.
  • Peg V; Translational Genomics and Targeted Therapeutics in Solid Tumors, August Pi i Sunyer Biomedical Research Institute, Barcelona, Spain.
  • Fasani R; SOLTI Breast Cancer Research Group, Barcelona, Spain.
  • Villagrasa P; Department of Medical Oncology, Hospital Clínic, Barcelona, Spain.
  • Gavilá J; Translational Genomics and Targeted Therapeutics in Solid Tumors, August Pi i Sunyer Biomedical Research Institute, Barcelona, Spain.
  • Barrios CH; SOLTI Breast Cancer Research Group, Barcelona, Spain.
  • Lluch A; Department of Medical Oncology, Hospital Clínic, Barcelona, Spain.
  • Martín M; Translational Genomics and Targeted Therapeutics in Solid Tumors, August Pi i Sunyer Biomedical Research Institute, Barcelona, Spain.
  • Locci M; Department of Genetics, University of North Carolina, Chapel Hill, NC, USA.
  • De Placido S; Translational Genomics and Targeted Therapeutics in Solid Tumors, August Pi i Sunyer Biomedical Research Institute, Barcelona, Spain.
  • Prat A; SOLTI Breast Cancer Research Group, Barcelona, Spain.
NPJ Breast Cancer ; 7(1): 1, 2021 Jan 04.
Article in En | MEDLINE | ID: mdl-33397968
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.

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: NPJ Breast Cancer Year: 2021 Document type: Article Affiliation country: Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: NPJ Breast Cancer Year: 2021 Document type: Article Affiliation country: Country of publication: