曲妥珠单抗
医学
乳腺癌
癌症研究
抗体-药物偶联物
抗体
单克隆抗体
癌细胞
癌症
肿瘤科
内科学
免疫学
作者
Miguel Martín,Atanasio Pandiella,Emilio Vargas,Elena Díaz‐Rodríguez,Teresa Iglesias-Hernangómez,Concha Martínez Cano,Inés Fernández-Cuesta,Elena Winkow,Maria Perelló
标识
DOI:10.1016/j.critrevonc.2024.104355
摘要
Trastuzumab deruxtecan (T-DXd) is an antibody-drug conjugate (ADC) consisting of a humanised, anti-human epidermal growth factor receptor 2 (HER2) monoclonal antibody covalently linked to a topoisomerase I inhibitor cytotoxic payload (DXd). The high drug-to-antibody ratio (8:1) ensures a high DXd concentration is delivered to target tumour cells, following internalisation of T-DXd and subsequent cleavage of its tetrapeptide-based linker. DXd's membrane-permeable nature enables it to cross cell membranes and potentially exert antitumour activity on surrounding tumour cells regardless of HER2 expression. T-DXd's unique mechanism of action is reflected in its efficacy in clinical trials in patients with HER2-positive advanced breast cancer (in heavily pretreated populations and in those previously treated with a taxane and trastuzumab), as well as HER2-low metastatic breast cancer. Thus, ADCs such as T-DXd have the potential to change the treatment paradigm of targeting HER2 in metastatic breast cancer, including eventually within the adjuvant/neoadjuvant setting.
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