Gogia Pooja, Ashraf Hamza, Bhasin Sidharth, Xu Yiqing
Department of Hematology/Oncology, Maimonides Medical Center, Brooklyn, NY 11219, USA.
Department of Internal Medicine, Overlook Medical Center, Summit, NJ 07901, USA.
Cancers (Basel). 2023 Jul 30;15(15):3886. doi: 10.3390/cancers15153886.
Antibody-drug conjugates (ADCs) are an innovative family of agents assembled through linking cytotoxic drugs (payloads) covalently to monoclonal antibodies (mAbs) to be delivered to tumor tissue that express their particular antigen, with the theoretical advantage of an augmented therapeutic ratio. As of June 2023, eleven ADCs have been approved by the Food and Drug Administration (FDA) and are on the market. These drugs have been added to the therapeutic armamentarium of acute myeloblastic and lymphoblastic leukemias, various types of lymphoma, breast, gastric or gastroesophageal junction, lung, urothelial, cervical, and ovarian cancers. They have proven to deliver more potent and effective anti-tumor activities than standard practice in a wide variety of indications. In addition to targeting antigen-expressing tumor cells, bystander effects have been engineered to extend cytotoxic killing to low-antigen-expressing or negative tumor cells in the heterogenous tumor milieu. Inevitably, myelosuppression is a common side effect with most of the ADCs due to the effects of the cytotoxic payload. Also, other unique side effects are specific to the tissue antigen that is targeted for, such as the cardiac toxicity with Her-2 targeting ADCs, and the hemorrhagic side effects with the tissue factor (TF) targeting Tisotumab vedotin. Further exciting developments are centered in the strategies to improve the tolerability and efficacy of the ADCs to improve the therapeutic window; as well as the development of novel payloads including (1) peptide-drug conjugates (PDCs), with the peptide replacing the monoclonal antibody, rendering greater tumor penetration; (2) immune-stimulating antibody conjugates (ISACs), which upon conjugation of the antigen, cause an influx of pro-inflammatory cytokines to activate dendritic cells and harness an anti-tumor T-cell response; and (3) the use of radioactive isotopes as a payload to enhance cytotoxic activity.
抗体药物偶联物(ADCs)是一类创新型药物,通过将细胞毒性药物(有效载荷)与单克隆抗体(mAbs)共价连接而成,可将其递送至表达特定抗原的肿瘤组织,理论上具有提高治疗指数的优势。截至2023年6月,已有11种ADC药物获得美国食品药品监督管理局(FDA)批准并上市。这些药物已被纳入急性髓细胞性和淋巴细胞性白血病、各类淋巴瘤、乳腺癌、胃癌或胃食管交界癌、肺癌、尿路上皮癌、宫颈癌和卵巢癌的治疗手段中。在多种适应症中,它们已被证明比标准治疗方法具有更强、更有效的抗肿瘤活性。除了靶向表达抗原的肿瘤细胞外,还设计了旁观者效应,以将细胞毒性杀伤作用扩展至异质性肿瘤环境中低表达或不表达抗原的肿瘤细胞。不可避免的是,由于细胞毒性有效载荷的作用,骨髓抑制是大多数ADC药物常见的副作用。此外,其他独特的副作用则特定于所靶向的组织抗原,例如靶向Her-2的ADC药物会导致心脏毒性,而靶向组织因子(TF)的替索单抗韦托辛会引起出血性副作用。进一步令人兴奋的进展集中在提高ADC药物耐受性和疗效以改善治疗窗口的策略上;以及新型有效载荷的开发,包括(1)肽-药物偶联物(PDCs),其中肽取代了单克隆抗体,具有更强的肿瘤穿透能力;(2)免疫刺激抗体偶联物(ISACs),在与抗原结合后,会引起促炎细胞因子的流入,从而激活树突状细胞并引发抗肿瘤T细胞反应;(3)使用放射性同位素作为有效载荷以增强细胞毒性活性。