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Editorial
. 2024 Sep;12(3):363-373.
doi: 10.1007/s40487-024-00286-3. Epub 2024 Jun 28.

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

Affiliations
Editorial

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

Luca Scafuri et al. Oncol Ther. 2024 Sep.

Abstract

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: 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: 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: 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.

Keywords: Breast cancer; Estrogen receptor-positive; HER2-low; Neoadjuvant therapy; Trastuzumab deruxtecan.

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Conflict of interest statement

Luca Scafuri and Carlo Buonerba have received honoraria as speakers from Genetic Spa. Vincenzo Di Lauro has received speaker’s honoraria from Amgen, Seagen, Wavepharma, Genetic, Veracyte, Novartis, and Accord. Paolo Tarantino reports research funding (to institution) from AstraZeneca and has served as advisor/consultant for AstraZeneca, Daiichi-Sankyo, Gilead, Novartis, Roche, Genentech and Lilly. Giuseppe Di Lorenzo is an Editorial Board member of Oncology and Therapy; he was not involved in the selection of peer reviewers for the manuscript nor any of the subsequent editorial decisions. Antonio Marra has received honoraria as a consultant, advisor or speaker from Roche and Menarini/Stemline; and has received travel and accommodation support from AstraZeneca. Vincenzo Tortora, Marco Cascella, Luigi Liguori, Antonella Sciarra, Francesco Sabbatino, Anna Diana, Dario Trapani, Mario Giuliano, Grazia Arpino and Giuseppe Curigliano have nothing to disclose.

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