a Division of Medical Oncology , University of Colorado , Aurora , CO , USA.
b Department of Internal Medicine , University of Colorado , Aurora , CO , USA.
Expert Opin Investig Drugs. 2018 Nov;27(11):901-916. doi: 10.1080/13543784.2018.1541085. Epub 2018 Nov 11.
Antibody drug conjugates (ADCs) represent a developing class of anticancer therapeutics which are designed to selectively deliver a cytotoxic payload to tumors, while limiting systemic toxicity to healthy tissues. There are several ADCs which are currently in various stages of clinical development for the treatment of gastrointestinal malignancies.
We discuss the biologic rationale and review the clinical experience with ADCs in the treatment of gastrointestinal malignancies, summarizing the pre-clinical and phase I/II clinical trial data that have been completed or are ongoing.
While there have been significant advances in the development of ADCs since they were first introduced, several challenges remain. These challenges include (i) the selection of an ideal antigen target which is tumor specific and internalized upon binding, (ii) selection of an antibody which has high affinity for its antigen target and low immunogenicity, (iii) selection of a potent payload which is cytotoxic at sub-nanomolar concentrations, and (iv) optimal design of a linker to confer ADC stability with limited off-site toxicity. Efforts are ongoing to address these issues and innovate the ADC technology to improve the safety and efficacy of these agents.
抗体药物偶联物(ADCs)是一类新兴的抗癌治疗药物,旨在将细胞毒性有效载荷选择性递送至肿瘤,同时将全身毒性限制在健康组织内。目前有几种 ADC 正在进行不同阶段的胃肠道恶性肿瘤治疗的临床试验。
我们讨论了 ADC 在胃肠道恶性肿瘤治疗中的生物学原理,并回顾了临床经验,总结了已完成或正在进行的临床前和 I/II 期临床试验数据。
自首次引入 ADC 以来,在其开发方面取得了重大进展,但仍存在一些挑战。这些挑战包括:(i)选择理想的抗原靶点,该靶点在结合后具有肿瘤特异性和内化性;(ii)选择对其抗原靶点具有高亲和力和低免疫原性的抗体;(iii)选择具有亚纳摩尔浓度细胞毒性的有效载荷;(iv)最佳设计连接子以赋予 ADC 稳定性,同时限制非靶毒性。目前正在努力解决这些问题并创新 ADC 技术,以提高这些药物的安全性和疗效。