State Key Laboratory of Complex Severe and Rare Diseases, NMPA Key Laboratory for Clinical Research and Evaluation of Drug, Beijing Key Laboratory of Clinical PK & PD Investigation for Innovative Drugs, Clinical Pharmacology Research Center, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, 100730, China.
College of Pharmacy, Shenyang Pharmaceutical University, Shenyang, Liaoning, 110016, China.
Clin Pharmacokinet. 2024 Oct;63(10):1373-1387. doi: 10.1007/s40262-024-01423-x. Epub 2024 Sep 26.
Antibody-drug conjugates (ADCs) have become a pivotal area in the research and development of antitumor drugs. They provide innovative possibilities for tumor therapy by integrating the tumor-targeting capabilities of monoclonal antibodies with the cytotoxic effect of small molecule drugs. Pharmacometrics, an important discipline, facilitates comprehensive understanding of the pharmacokinetic characteristics of ADCs by integrating clinical trial data through modeling and simulation. However, due to the complex structure of ADCs, their modeling approaches are still unclear. In this review, we analyzed published population pharmacokinetic models for ADCs and classified them into single-analyte, two-analyte, and three-analyte models. We also described the benefits, limitations, and recommendations for each model. Furthermore, we suggested that the development of population pharmacokinetic models for ADCs should be rigorously considered and established based on four key aspects: (1) research objectives; (2) available in vitro and animal data; (3) accessible clinical information; and (4) the capability of bioanalytical methods. This review offered insights to guide the application of pharmacometrics in the clinical research of ADCs, thereby contributing to more effective therapeutic development.
抗体偶联药物(ADCs)已成为抗肿瘤药物研发的一个关键领域。它们通过将单克隆抗体的肿瘤靶向能力与小分子药物的细胞毒性作用相结合,为肿瘤治疗提供了创新的可能性。药物代谢动力学是一门重要的学科,它通过建模和模拟整合临床试验数据,有助于全面了解 ADC 的药代动力学特征。然而,由于 ADC 的复杂结构,其建模方法仍不清楚。在本综述中,我们分析了已发表的 ADC 群体药代动力学模型,并将其分为单分析物、双分析物和三分析物模型。我们还描述了每种模型的优点、局限性和建议。此外,我们建议应严格考虑并基于四个关键方面来建立 ADC 的群体药代动力学模型:(1)研究目标;(2)可用的体外和动物数据;(3)可获得的临床信息;以及(4)生物分析方法的能力。本综述提供了指导药物代谢动力学在 ADC 临床研究中应用的见解,从而有助于更有效的治疗药物开发。