Scafuri Luca, Buonerba Carlo, Di Lauro Vincenzo, Tortora Vincenzo, Cascella Marco, Liguori Luigi, Sciarra Antonella, Sabbatino Francesco, Diana Anna, Marra Antonio, Tarantino Paolo, Trapani Dario, Giuliano Mario, Arpino Grazia, Curigliano Giuseppe, Di Lorenzo Giuseppe
Oncology Unit, "Andrea Tortora" Hospital, ASL Salerno, Pagani, Italy.
Associazione O.R.A. ETS-Oncology Research Assistance, Salerno, Italy.
Oncol Ther. 2024 Sep;12(3):363-373. doi: 10.1007/s40487-024-00286-3. Epub 2024 Jun 28.
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.
乳腺癌呈现出多种分子亚型,影响着治疗策略。人表皮生长因子受体2(HER2)低表达、激素受体阳性(HR+)的乳腺癌由于靶向治疗有限而构成挑战。目前的新辅助治疗主要采用化疗,对于HER2低表达乳腺癌患者的疗效结果存在矛盾。曲妥珠单抗德曲妥珠单抗(T-DXd)在HER2低表达转移性疾病中显示出前景,初步证据表明其与内分泌治疗具有协同作用。
本社论探讨新辅助T-DXd联合或不联合内分泌治疗在HR+/HER2低表达乳腺癌临床管理中具有疗效的假设。
我们提出一项II期研究,设有两个治疗组:T-DXd+来曲唑组和单独使用T-DXd组。主要终点是放射学完全缓解率。次要终点包括病理完全缓解率、安全性、无事件生存期和总生存期。探索性分析将比较两组,以确定优化治疗疗效和最小化副作用的潜力。
本研究设计允许对T-DXd联合或不联合内分泌治疗HER2低表达乳腺癌进行初步评估。这些发现可能为个性化治疗策略铺平道路,并为未来研究提供信息,有可能导致一种避免化疗的方法。