Exploring a Novel Approach to Spare Classic Chemotherapy in HER2-Low, ER-Positive Breast Cancer Based on Trastuzumab Deruxtecan Combined with Endocrine Therapy.

Breast cancer Estrogen receptor-positive HER2-low Neoadjuvant therapy Trastuzumab deruxtecan

Journal

Oncology and therapy
ISSN: 2366-1089
Titre abrégé: Oncol Ther
Pays: New Zealand
ID NLM: 101677510

Informations de publication

Date de publication:
28 Jun 2024
Historique:
received: 21 03 2024
accepted: 03 06 2024
medline: 28 6 2024
pubmed: 28 6 2024
entrez: 28 6 2024
Statut: aheadofprint

Résumé

Breast cancer presents diverse molecular subtypes affecting treatment strategies. Human epidermal growth factor receptor 2 (HER2)-low, hormone receptor-positive (HR+) breast cancer poses a challenge due to limited targeted therapies. Current neoadjuvant treatment primarily utilizes chemotherapy, with conflicting results regarding efficacy in patients with HER2-low breast cancer. Trastuzumab deruxtecan (T-DXd) shows promise in HER2-low metastatic disease, and preliminary evidence suggests synergy with endocrine therapy. This editorial explores the hypothesis that neoadjuvant T-DXd with or without endocrine therapy offers efficacy in the clinical management of HR+/HER2-low breast cancer. We propose a phase II study with two treatment arms: T-DXd + letrozole and T-DXd alone. The primary endpoint is the radiological complete response rate. Secondary endpoints include pathological complete response rate, safety, event-free survival, and overall survival. Exploratory analyses will compare the arms to identify potential for optimizing treatment efficacy and minimizing side effects. This study design allows for initial assessment of T-DXd with or without endocrine therapy in the treatment of HER2-low breast cancer. The findings may pave the way for personalized treatment strategies and inform future research, potentially leading to a chemotherapy-sparing approach.

Sections du résumé

BACKGROUND BACKGROUND
Breast cancer presents diverse molecular subtypes affecting treatment strategies. Human epidermal growth factor receptor 2 (HER2)-low, hormone receptor-positive (HR+) breast cancer poses a challenge due to limited targeted therapies. Current neoadjuvant treatment primarily utilizes chemotherapy, with conflicting results regarding efficacy in patients with HER2-low breast cancer. Trastuzumab deruxtecan (T-DXd) shows promise in HER2-low metastatic disease, and preliminary evidence suggests synergy with endocrine therapy.
OBJECTIVE OBJECTIVE
This editorial explores the hypothesis that neoadjuvant T-DXd with or without endocrine therapy offers efficacy in the clinical management of HR+/HER2-low breast cancer.
METHODS METHODS
We propose a phase II study with two treatment arms: T-DXd + letrozole and T-DXd alone. The primary endpoint is the radiological complete response rate. Secondary endpoints include pathological complete response rate, safety, event-free survival, and overall survival. Exploratory analyses will compare the arms to identify potential for optimizing treatment efficacy and minimizing side effects.
CONCLUSIONS CONCLUSIONS
This study design allows for initial assessment of T-DXd with or without endocrine therapy in the treatment of HER2-low breast cancer. The findings may pave the way for personalized treatment strategies and inform future research, potentially leading to a chemotherapy-sparing approach.

Identifiants

pubmed: 38941050
doi: 10.1007/s40487-024-00286-3
pii: 10.1007/s40487-024-00286-3
doi:

Types de publication

Editorial

Langues

eng

Informations de copyright

© 2024. The Author(s).

Références

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Auteurs

Luca Scafuri (L)

Oncology Unit, "Andrea Tortora" Hospital, ASL Salerno, Pagani, Italy. lucaluca@hotmail.it.
Associazione O.R.A. ETS-Oncology Research Assistance, Salerno, Italy. lucaluca@hotmail.it.

Carlo Buonerba (C)

Oncology Unit, "Andrea Tortora" Hospital, ASL Salerno, Pagani, Italy.
Associazione O.R.A. ETS-Oncology Research Assistance, Salerno, Italy.

Vincenzo Di Lauro (V)

Department of Breast & Thoracic Oncology, Division of Breast Medical Oncology, Istituto Nazionale Tumori IRCCS "Fondazione G. Pascale", Naples, Italy.

Vincenzo Tortora (V)

S.C. Oncologia, ASL Vercelli, Vercelli, Italy.

Marco Cascella (M)

Anesthesia and Pain Medicine, Department of Medicine, Surgery and Dentistry "Scuola Medica Salernitana", University of Salerno, Via S. Allende, 84081, Baronissi, Italy.

Luigi Liguori (L)

Department of Clinical Medicine and Surgery, University of Naples Federico II, Naples, Italy.

Antonella Sciarra (A)

Department of Experimental Medicine, University of Campania 'Luigi Vanvitelli', Naples, NA, Italy.

Francesco Sabbatino (F)

Oncology Unit, Department of Medicine, Surgery and Dentistry, University of Salerno, 84081, Baronissi, Salerno, Italy.

Anna Diana (A)

Medical Oncology Unit, Ospedale del Mare, Naples, Italy.

Antonio Marra (A)

European Institute of Oncology-IRCCS, Milan, Italy.

Paolo Tarantino (P)

Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Breast Oncology Program, Dana-Farber Brigham Cancer Center, Boston, MA, USA.
Harvard Medical School, Boston, MA, USA.
Department of Oncology and Hemato-Oncology, University of Milan, Milan, Italy.

Dario Trapani (D)

Department of Oncology and Hemato-Oncology, University of Milan, Milan, Italy.
Division of Early Drug Development for Innovative Therapy, European Institute of Oncology-IRCCS, Milan, Italy.

Mario Giuliano (M)

Department of Clinical Medicine and Surgery, University of Naples Federico II, Naples, Italy.

Grazia Arpino (G)

Department of Clinical Medicine and Surgery, University of Naples Federico II, Naples, Italy.

Giuseppe Curigliano (G)

Department of Oncology and Hemato-Oncology, University of Milan, Milan, Italy.
Division of Early Drug Development for Innovative Therapy, European Institute of Oncology-IRCCS, Milan, Italy.

Giuseppe Di Lorenzo (G)

Oncology Unit, "Andrea Tortora" Hospital, ASL Salerno, Pagani, Italy.
Associazione O.R.A. ETS-Oncology Research Assistance, Salerno, Italy.

Classifications MeSH