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DESTINY-Breast Respond HER2-low 欧洲研究设计:T-DXd 在 HER2 低表达晚期乳腺癌患者中的应用。

Study design for DESTINY-Breast Respond HER2-low Europe: T-DXd in patients with HER2-low advanced breast cancer.

机构信息

Medical Oncology 2, Veneto Institute of Oncology (IOV), IRCCS, Via Gattamelata, 64, 35128 Padova PD, Italy.

Department of Surgery, Oncology & Gastroenterology, University of Padova, Via Nicolò Giustiniani, 2, 35128 Padova PD, Italy.

出版信息

Future Oncol. 2024;20(18):1237-1250. doi: 10.2217/fon-2024-0015. Epub 2024 Apr 9.

Abstract

Trastuzumab deruxtecan (T-DXd) is approved for the treatment of human epidermal growth factor receptor 2 (HER2)-low metastatic breast cancer (mBC). Results on T-DXd treatment in HER2-low mBC have so far been limited to clinical trials. DESTINY-Breast Respond HER2-low Europe (NCT05945732) is a multi-center, multi-country, observational, prospective, non-interventional study planning to enroll 1350 patients from 216 sites receiving T-DXd or conventional chemotherapy as their routine clinical care for advanced stage breast cancer in 12 European countries. This non-interventional study will provide real-world insight into T-DXd treatment for HER2-low mBC with data on effectiveness, safety and tolerability, patient-reported outcomes, treatment patterns, geriatric health status and HER2 testing. This will be beneficial for improving guidance to maximize patient treatment benefit.

摘要

曲妥珠单抗-德鲁替康(T-DXd)获批用于治疗人表皮生长因子受体 2(HER2)低转移性乳腺癌(mBC)。迄今为止,HER2 低水平 mBC 中 T-DXd 治疗的结果仅限于临床试验。DESTINY-Breast Respond HER2-low Europe(NCT05945732)是一项多中心、多国、观察性、前瞻性、非干预性研究,计划从 12 个欧洲国家的 216 个地点招募 1350 名接受 T-DXd 或常规化疗的患者,作为其晚期乳腺癌常规临床治疗的一部分。这项非干预性研究将通过对有效性、安全性和耐受性、患者报告结果、治疗模式、老年健康状况和 HER2 检测的数据,为 HER2 低水平 mBC 的 T-DXd 治疗提供真实世界的见解。这将有助于改善指导意见,以最大限度地提高患者的治疗获益。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d4ba/11318675/a7e5d52f4e6c/IFON_A_2339007_F0001_C.jpg

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