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在缺乏药代动力学采样的情况下,利用凝血酶原时间提高利伐沙班暴露量估算的质量。

Enhancing the Quality of Rivaroxaban Exposure Estimates Using Prothrombin Time in the Absence of Pharmacokinetic Sampling.

机构信息

Clinical Pharmacometrics, Bayer AG, Berlin, Germany.

Statistical Analytics Clinical Sciences, Bayer AG, Wuppertal, Germany.

出版信息

CPT Pharmacometrics Syst Pharmacol. 2019 Nov;8(11):805-814. doi: 10.1002/psp4.12444. Epub 2019 Jul 5.

Abstract

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.

摘要

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。

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