Institute of Pharmaceutical Sciences, Department of Chemistry and Applied Biosciences, ETH Zürich, Vladimir-Prelog-Weg 1-5/10, CH 8053, Zurich, Switzerland.
SENN Chemicals AG, Guido Senn-Strasse 1, CH 8157, Dielsdorf, Switzerland.
Pharmacol Ther. 2016 Nov;167:48-59. doi: 10.1016/j.pharmthera.2016.07.012. Epub 2016 Aug 2.
Conventional cytotoxic agents used for the pharmacotherapy of cancer do not selectively localize at the tumor site, which may prevent dose escalation to therapeutically active regimens and may lead to undesired side effects and toxicity to normal organs. There has been a growing interest in the use of monoclonal antibodies as vehicles for the pharmacodelivery of potent cytotoxic drugs to neoplastic lesions. This novel class of targeted biopharmaceutical agents has the potential of improving activity and selectivity of cytotoxic agents. However, many technical aspects contribute to the success or failure of antibody-drug conjugates (ADCs). In this review, we summarize important pre-clinical and clinical examples of early and current improvements in the field ADCs, including diversification of payloads, linkers, conjugation technologies, ADC formats and type of targets. Combination therapies of ADCs with checkpoint inhibitors are also discussed, in light of the exceptional expansion recorded in the latter space over the last five years.
传统的细胞毒性药物用于癌症的药物治疗不能选择性地定位在肿瘤部位,这可能阻止剂量增加到治疗有效的方案,并可能导致不期望的副作用和对正常器官的毒性。人们越来越关注使用单克隆抗体作为载体,将有效的细胞毒性药物递送到肿瘤病变部位。这种新型靶向生物制药有提高细胞毒性药物的活性和选择性的潜力。然而,许多技术方面影响抗体药物偶联物(ADC)的成败。在这篇综述中,我们总结了 ADC 领域早期和当前改进的重要临床前和临床实例,包括有效载荷、连接子、偶联技术、ADC 形式和靶点类型的多样化。还讨论了 ADC 与检查点抑制剂的联合治疗,考虑到过去五年后者领域的显著扩张。