布仑妥昔单抗维多汀
奥佐美星
医学
卡奇霉素
曲妥珠单抗
曲妥珠单抗
抗体-药物偶联物
结合
临床试验
药品
肿瘤科
药理学
抗体
药物开发
内科学
单克隆抗体
淋巴瘤
髓系白血病
药物输送
癌症
药物发现
靶向给药
药代动力学
免疫原性
抗原
体内
化学
小分子
乳腺癌
免疫学
霍奇金淋巴瘤
CD33
生物
遗传学
干细胞
川地34
作者
Pengxuan Zhao,Yuebao Zhang,Wenqing Li,Christopher Jeanty,Guangya Xiang,Yizhou Dong
标识
DOI:10.1016/j.apsb.2020.04.012
摘要
Antibody drug conjugates (ADCs) normally compose of a humanized antibody and small molecular drug via a chemical linker. After decades of preclinical and clinical studies, a series of ADCs have been widely used for treating specific tumor types in the clinic such as brentuximab vedotin (Adcetris®) for relapsed Hodgkin's lymphoma and systemic anaplastic large cell lymphoma, gemtuzumab ozogamicin (Mylotarg®) for acute myeloid leukemia, ado-trastuzumab emtansine (Kadcyla®) for HER2-positive metastatic breast cancer, inotuzumab ozogamicin (Besponsa®) and most recently polatuzumab vedotin-piiq (Polivy®) for B cell malignancies. More than eighty ADCs have been investigated in different clinical stages from approximately six hundred clinical trials to date. This review summarizes the key elements of ADCs and highlights recent advances of ADCs, as well as important lessons learned from clinical data, and future directions.
科研通智能强力驱动
Strongly Powered by AbleSci AI