Díaz-Rodríguez Elena, Gandullo-Sánchez Lucía, Ocaña Alberto, Pandiella Atanasio
Instituto de Biología Molecular y Celular del Cáncer, CSIC-IBSAL and CIBERONC, 37007 Salamanca, Spain.
Departamento de Bioquímica y Biología Molecular, University of Salamanca, 37007 Salamanca, Spain.
Cancers (Basel). 2021 Dec 29;14(1):154. doi: 10.3390/cancers14010154.
During recent years, a number of new compounds against HER2 have reached clinics, improving the prognosis and quality of life of HER2-positive breast cancer patients. Nonetheless, resistance to standard-of-care drugs has motivated the development of novel agents, such as new antibody-drug conjugates (ADCs). The latter are a group of drugs that benefit from the potency of cytotoxic agents whose action is specifically guided to the tumor by the target-specific antibody. Two anti-HER2 ADCs have reached the clinic: trastuzumab-emtansine and, more recently, trastuzumab-deruxtecan. In addition, several other HER2-targeted ADCs are in preclinical or clinical development, some of them with promising signs of activity. In the present review, the structure, mechanism of action, and potential resistance to all these ADCs will be described. Specific attention will be given to discussing novel strategies to circumvent resistance to ADCs.
近年来,多种针对HER2的新型化合物已进入临床,改善了HER2阳性乳腺癌患者的预后和生活质量。尽管如此,对标准治疗药物的耐药性促使了新型药物的研发,如新的抗体药物偶联物(ADC)。后者是一类药物,受益于细胞毒性药物的效力,其作用通过靶向特异性抗体被特异性引导至肿瘤。两种抗HER2 ADC已进入临床:曲妥珠单抗-恩杂鲁胺,以及最近的曲妥珠单抗-德曲妥珠单抗。此外,其他几种靶向HER2的ADC正处于临床前或临床开发阶段,其中一些具有有前景的活性迹象。在本综述中,将描述所有这些ADC的结构、作用机制和潜在耐药性。将特别关注讨论规避ADC耐药性的新策略。