Esapa Benjamina, Jiang Jiexuan, Cheung Anthony, Chenoweth Alicia, Thurston David E, Karagiannis Sophia N
St. John's Institute of Dermatology, School of Basic & Medical Biosciences, King's College London, Guy's Hospital, London SE1 9RT, UK.
Breast Cancer Now Research Unit, School of Cancer & Pharmaceutical Sciences, King's College London, Guy's Cancer Centre, London SE1 9RT, UK.
Cancers (Basel). 2023 Mar 19;15(6):1845. doi: 10.3390/cancers15061845.
Antibody drug conjugates (ADCs) are powerful anti-cancer therapies comprising an antibody joined to a cytotoxic payload through a chemical linker. ADCs exploit the specificity of antibodies for their target antigens, combined with the potency of cytotoxic drugs, to selectively kill target antigen-expressing tumour cells. The recent rapid advancement of the ADC field has so far yielded twelve and eight ADCs approved by the US and EU regulatory bodies, respectively. These serve as effective targeted treatments for several haematological and solid tumour types. In the development of an ADC, the judicious choice of an antibody target antigen with high expression on malignant cells but restricted expression on normal tissues and immune cells is considered crucial to achieve selectivity and potency while minimising on-target off-tumour toxicities. Aside from this paradigm, the selection of an antigen for an ADC requires consideration of several factors relating to the expression pattern and biological features of the target antigen. In this review, we discuss the attributes of antigens selected as targets for antibodies used in clinically approved ADCs for the treatment of haematological and solid malignancies. We discuss target expression, functions, and cellular kinetics, and we consider how these factors might contribute to ADC efficacy.
抗体药物偶联物(ADCs)是一种强大的抗癌疗法,它由通过化学连接子连接到细胞毒性有效载荷的抗体组成。ADCs利用抗体对其靶抗原的特异性,结合细胞毒性药物的效力,选择性地杀死表达靶抗原的肿瘤细胞。ADC领域最近的快速发展迄今已分别产生了12种和8种获美国和欧盟监管机构批准的ADC。这些ADC可作为多种血液系统和实体瘤类型的有效靶向治疗药物。在ADC的开发中,明智地选择在恶性细胞上高表达但在正常组织和免疫细胞上表达受限的抗体靶抗原,被认为对于实现选择性和效力,同时将靶上非肿瘤毒性降至最低至关重要。除了这种模式外,为ADC选择抗原还需要考虑与靶抗原的表达模式和生物学特性相关的几个因素。在这篇综述中,我们讨论了被选作治疗血液系统和实体恶性肿瘤的临床批准ADC中使用的抗体靶标的抗原的特性。我们讨论了靶标表达、功能和细胞动力学,并考虑了这些因素可能如何有助于ADC的疗效。