Liu C, Yu J, Li H, Liu J, Xu Y, Song P, Liu Q, Zhao H, Xu J, Maher V E, Booth B P, Kim G, Rahman A, Wang Y
Food and Drug Administration, Silver Spring, Maryland, USA.
Clin Pharmacol Ther. 2017 May;101(5):657-666. doi: 10.1002/cpt.656. Epub 2017 Mar 22.
Nivolumab is a human monoclonal antibody that blocks the interaction between PD-1 programmed death-1 (PD-1) and its ligands, PD-L1 and PD-L2. Nivolumab demonstrated efficacy in clinical trials for various types of cancer. A time-varying clearance was identified for nivolumab. We show that the change of clearance over time is associated with the post-treatment effects: clearance decreases when disease status improves. This interaction between posttreatment effects and drug exposure may lead to a biased steep estimate of the exposure-response (E-R) relationship for efficacy. Under this scenario, simulations were performed to develop a proposed methodology to assess the causal effect of drug exposure upon clinical response. Data from nivolumab trials were subsequently used to verify the proposed methodology for E-R analysis. The results showed that E-R analysis results based on pharmacokinetic (PK) metrics derived from the first dose are more consistent with the true E-R or dose-response relationship than the steady-state PK metrics.
纳武单抗是一种人源单克隆抗体,可阻断程序性死亡受体1(PD-1)与其配体PD-L1和PD-L2之间的相互作用。纳武单抗在各类癌症的临床试验中均显示出疗效。已确定纳武单抗存在时变清除率。我们发现清除率随时间的变化与治疗后的效果相关:疾病状态改善时清除率降低。治疗后效果与药物暴露之间的这种相互作用可能会导致对疗效的暴露-反应(E-R)关系的估计出现偏差且过于陡峭。在这种情况下,进行了模拟以开发一种评估药物暴露对临床反应因果效应的方法。随后使用纳武单抗试验的数据来验证所提出的E-R分析方法。结果表明,基于首剂药代动力学(PK)指标的E-R分析结果比稳态PK指标更符合真实的E-R或剂量-反应关系。