Na Joo Young, Jeon Juyeun, Huh Ki Young, Yu Kyung-Sang, Lee Sangmi, Eom Jaehyun, Ahn Jinhyung, You Weon-Kyoo, Oh Jaeseong
Department of Clinical Pharmacology and Therapeutics, Seoul National University College of Medicine and Hospital, Seoul, Republic of Korea.
Division of Pharmaceutics and Pharmacology, College of Pharmacy, The Ohio State University, Columbus, Ohio, USA.
Cancer Sci. 2024 Dec;115(12):3943-3951. doi: 10.1111/cas.16363. Epub 2024 Oct 7.
ABL001/CTX-009 is a bispecific antibody targeting delta-like ligand-4 and vascular endothelial growth factor A. In this study, we developed a population pharmacokinetic (PK) model of ABL001/CTX-009 in patients with solid tumors. A total of 712 plasma concentrations from 30 patients with relapsed or refractory solid tumors were collected from a phase 1 study (NCT03292783). A population PK model was developed using a nonlinear mixed-effect method and was evaluated by graphical and numerical methods. Using the model, the steady-state concentrations were simulated to compare weight-based and fixed-dose regimens and to find optimal dosing intervals. The PK of ABL001/CTX-009 was well described by a two-compartment model with a parallel first-order and Michaelis-Menten elimination kinetics. Body weight was selected as a significant covariate on V1. Model evaluation results suggested that the model was adequate and robust with good precision. Simulations after administrations of fixed or weight-based doses showed similar plasma concentrations. Additionally, 10 mg/kg for every other week and 15 mg/kg for every three-week administration showed comparable plasma concentrations. In conclusion, the model well described the plasma concentrations of ABL001/CTX-009 in patients with solid tumors. The simulation suggested that weight-based dose and fixed dose can provide equivalent systemic exposure.
ABL001/CTX-009是一种靶向Delta样配体-4和血管内皮生长因子A的双特异性抗体。在本研究中,我们建立了实体瘤患者中ABL001/CTX-009的群体药代动力学(PK)模型。从一项1期研究(NCT03292783)中收集了30例复发或难治性实体瘤患者的总共712份血浆浓度。使用非线性混合效应方法建立了群体PK模型,并通过图形和数值方法进行了评估。利用该模型,模拟稳态浓度以比较基于体重的给药方案和固定剂量方案,并找出最佳给药间隔。ABL001/CTX-009的药代动力学通过具有平行一级和米氏消除动力学的二室模型得到了很好的描述。体重被选为对V1有显著影响的协变量。模型评估结果表明该模型足够且稳健,精度良好。给予固定剂量或基于体重的剂量后的模拟显示血浆浓度相似。此外,每隔一周10mg/kg和每三周15mg/kg的给药方案显示出相当的血浆浓度。总之,该模型很好地描述了实体瘤患者中ABL001/CTX-009的血浆浓度。模拟表明基于体重的剂量和固定剂量可提供等效的全身暴露。