Clinical Pharmacometrics, Bayer AG, Berlin, Germany.
Statistical Analytics Clinical Sciences, Bayer AG, Wuppertal, Germany.
CPT Pharmacometrics Syst Pharmacol. 2019 Nov;8(11):805-814. doi: 10.1002/psp4.12444. Epub 2019 Jul 5.
Prothrombin time (PT) is a measure of coagulation status and was assessed in the majority of patients in the rivaroxaban phase II and III clinical trials as a pharmacodynamic marker. In the absence of sufficient phase III pharmacokinetic (PK) data to provide individual exposure measures for input into rivaroxaban exposure-response analyses, the aim of the present study was to investigate the use of PT-adjustment approaches (i.e., the use of observed individual PT measurements) to enhance the prediction of individual rivaroxaban exposure metrics (derived using a previously developed integrated population PK model) based on the observed linear relationship between PT and rivaroxaban plasma concentrations. The PT-adjustment approaches were established using time-matched PK and PT measurements, which were available from 1,779 patients across four phase II trials and one phase III trial of rivaroxaban. PT-adjusted exposure estimates improved the identification of statistically significant effects when compared with covariate-only exposure estimates.
凝血酶原时间(PT)是凝血状态的一种衡量标准,在利伐沙班的 II 期和 III 期临床试验中,大多数患者都将其作为药效学标志物进行评估。由于缺乏足够的 III 期药代动力学(PK)数据来提供个体暴露量的测量值,以便输入到利伐沙班暴露-反应分析中,因此本研究旨在探讨使用 PT 调整方法(即使用观察到的个体 PT 测量值)来增强对个体利伐沙班暴露量指标的预测(使用先前开发的综合人群 PK 模型进行推导),这是基于观察到的 PT 与利伐沙班血浆浓度之间的线性关系。使用来自四个 II 期试验和一个 III 期利伐沙班试验的 1779 名患者的时间匹配 PK 和 PT 测量值建立了 PT 调整方法。与仅使用协变量的暴露估计相比,PT 调整后的暴露估计可更好地识别具有统计学意义的影响。