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HER2-Low Breast Cancer: Molecular Characteristics and Prognosis.
Agostinetto, Elisa; Rediti, Mattia; Fimereli, Danai; Debien, Véronique; Piccart, Martine; Aftimos, Philippe; Sotiriou, Christos; de Azambuja, Evandro.
Afiliação
  • Agostinetto E; Academic Trials Promoting Team, Institut Jules Bordet, l'Université Libre de Bruxelles (U.L.B), 1000 Brussels, Belgium.
  • Rediti M; Humanitas Clinical and Research Center-IRCCS, Humanitas Cancer Center, Via Manzoni 56, 20089 Milan, Italy.
  • Fimereli D; Department of Biomedical Sciences, Humanitas University, Via Rita Levi Montalcini 4, 20090 Milan, Italy.
  • Debien V; Breast Cancer Translational Research Laboratory J.-C. Heuson, Institut Jules Bordet, Université Libre de Bruxelles, 1000 Brussels, Belgium.
  • Piccart M; Breast Cancer Translational Research Laboratory J.-C. Heuson, Institut Jules Bordet, Université Libre de Bruxelles, 1000 Brussels, Belgium.
  • Aftimos P; Academic Trials Promoting Team, Institut Jules Bordet, l'Université Libre de Bruxelles (U.L.B), 1000 Brussels, Belgium.
  • Sotiriou C; Medical Oncology Department, Institut Jules Bordet, 1000 Brussels, Belgium.
  • de Azambuja E; Clinical Trials Conduct Unit, Institut Jules Bordet-Université Libre de Bruxelles, 1000 Brussels, Belgium.
Cancers (Basel) ; 13(11)2021 Jun 05.
Article em En | MEDLINE | ID: mdl-34198891
ABSTRACT

BACKGROUND:

We aimed to determine the distribution of intrinsic subtypes within HER2-low breast cancer (BC), and to describe the prognostic impact of HER2-low status on survival outcomes.

METHODS:

This is a retrospective, observational study of primary BC extracted from The Cancer Genome Atlas dataset. We described the distribution of PAM50 intrinsic subtypes within HER2-low BC subtype according to hormonal receptor status (positive (HR+) and negative (HR-)). Secondly, we assessed the impact of HER2-low on survival outcomes (progression-free interval (PFI), disease-free interval (DFI), and overall survival (OS)).

RESULTS:

We analyzed 804 primary BCs, including 410 (51%) HER2-low BCs (336 HR+ and 74 HR-). The proportion of HER2-enriched tumors was higher in the HER2-low/HR- group compared to HER2-low/HR+ (13.7% versus 1.2%, respectively). HER2-enriched tumors were more frequent in HER2-low/HR- and HER2-low/HR+ subtypes, compared to HER2-negative/HR- and HER2-negative/HR+ subtypes, respectively (13.7% versus 1.6% and 1.2% versus 0.5%, respectively). We observed no significant differences in PFI, DFI, and OS between HER2-low subtypes and each non-HER2-low subtype paired by HR status.

CONCLUSIONS:

Our characterization of PAM50 intrinsic subtypes within HER2-low breast cancer may explain the different clinical behaviors and responses to treatment, and ultimately support further investigation of new treatment strategies in the HER2-low category. Moreover, it highlights the importance of considering HR status in the HER2-low category.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Observational_studies / Prognostic_studies Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Observational_studies / Prognostic_studies Idioma: En Ano de publicação: 2021 Tipo de documento: Article