Blair Hannah A
Springer Nature, Private Bag 65901, Mairangi Bay, Auckland, 0754, New Zealand.
Drugs. 2025 May 5. doi: 10.1007/s40265-025-02185-x.
Datopotamab deruxtecan (DATROWAY) is a trophoblast cell surface antigen 2 (TROP2)-directed antibody-drug conjugate being developed by Daiichi Sankyo and AstraZeneca for the treatment of solid tumours. On 27 December 2024, datopotamab deruxtecan was approved in Japan for the treatment of adult patients with hormone receptor (HR) positive, human epidermal growth factor receptor 2 (HER2) negative unresectable or recurrent breast cancer after prior chemotherapy. The drug has since been approved on 17 January 2025 in the USA for the treatment of adult patients with unresectable or metastatic HR positive, HER2 negative breast cancer who have received prior endocrine-based therapy and chemotherapy for unresectable or metastatic disease. Datopotamab deruxtecan has also been approved in the EU for the treatment of adult patients with unresectable or metastatic HR positive, HER2 negative breast cancer who have received endocrine therapy and at least one line of chemotherapy in the advanced setting. Regulatory review of datopotamab deruxtecan in breast cancer is underway in Canada and China. This article summarizes the milestones in the development of datopotamab deruxtecan leading to this first approval for the treatment of HR positive, HER2 negative breast cancer.
德曲妥珠单抗(DATROWAY)是一种由第一三共株式会社和阿斯利康共同开发的靶向滋养层细胞表面抗原2(TROP2)的抗体偶联药物,用于治疗实体瘤。2024年12月27日,德曲妥珠单抗在日本获批,用于治疗先前接受过化疗的激素受体(HR)阳性、人表皮生长因子受体2(HER2)阴性的不可切除或复发性乳腺癌成年患者。此后,该药物于2025年1月17日在美国获批,用于治疗接受过基于内分泌治疗和针对不可切除或转移性疾病的化疗的不可切除或转移性HR阳性、HER2阴性乳腺癌成年患者。德曲妥珠单抗在欧盟也已获批,用于治疗在晚期接受过内分泌治疗和至少一线化疗的不可切除或转移性HR阳性、HER2阴性乳腺癌成年患者。加拿大和中国正在对德曲妥珠单抗治疗乳腺癌进行监管审查。本文总结了德曲妥珠单抗开发过程中的里程碑事件,这些事件促成了其首次获批用于治疗HR阳性、HER2阴性乳腺癌。