Jang Jung Yoon, Kim Donghwan, Lee Na Kyeong, Im Eunok, Kim Nam Deuk
Department of Pharmacy, College of Pharmacy, Research Institute for Drug Development, Pusan National University, Busan 46241, Republic of Korea.
Functional Food Materials Research Group, Korea Food Research Institute, Wanju-gun 55365, Jeollabuk-do, Republic of Korea.
Int J Mol Sci. 2025 Jul 7;26(13):6523. doi: 10.3390/ijms26136523.
Antibody-drug conjugates (ADCs) have revolutionized precision oncology by enabling targeted drug delivery with improved therapeutic indices. Among these, deruxtecan (DXd)-based ADCs have demonstrated remarkable efficacy across a range of cancers, particularly in tumors expressing human epidermal growth factor receptor 2 (HER2), human epidermal growth factor receptor 3 (HER3), and trophoblast cell surface antigen 2 (TROP2), including breast, lung, gastric, and other solid tumors. DXd, a potent topoisomerase I inhibitor, enhances the cytotoxic potential of ADCs through a cleavable and stable linker and a high drug-to-antibody ratio that ensures optimal drug release. The clinical success of trastuzumab DXd (Enhertu) and datopotamab DXd (Datroway), along with the ongoing development of patritumab DXd, has expanded the therapeutic potential of ADCs. However, challenges remain, including toxicity, resistance, and manufacturing scalability. This review discusses the mechanisms of action, clinical progress, and challenges of DXd-based ADCs, highlighting their transformative role in modern oncology and exploring future directions to optimize their efficacy and accessibility.
抗体药物偶联物(ADCs)通过实现靶向给药并改善治疗指数,彻底改变了精准肿瘤学。其中,基于德曲妥珠单抗(DXd)的ADCs在一系列癌症中均显示出显著疗效,尤其是在表达人表皮生长因子受体2(HER2)、人表皮生长因子受体3(HER3)和滋养层细胞表面抗原2(TROP2)的肿瘤中,包括乳腺癌、肺癌、胃癌和其他实体瘤。DXd是一种强效拓扑异构酶I抑制剂,通过可裂解且稳定的连接子以及高药物抗体比增强ADCs的细胞毒性潜力,确保最佳药物释放。曲妥珠单抗DXd(Enhertu)和达泊妥单抗DXd(Datroway)的临床成功,以及帕妥珠单抗DXd的持续研发,扩大了ADCs的治疗潜力。然而,挑战依然存在,包括毒性、耐药性和生产可扩展性。本综述讨论了基于DXd的ADCs的作用机制、临床进展和挑战,突出了它们在现代肿瘤学中的变革性作用,并探索优化其疗效和可及性的未来方向。