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使用非参数估计法对侵袭性真菌病患者进行的艾沙康唑群体药代动力学分析(VITAL研究结果)

Isavuconazole Population Pharmacokinetic Analysis Using Nonparametric Estimation in Patients with Invasive Fungal Disease (Results from the VITAL Study).

作者信息

Kovanda Laura L, Desai Amit V, Lu Qiaoyang, Townsend Robert W, Akhtar Shahzad, Bonate Peter, Hope William W

机构信息

Antimicrobial Pharmacodynamics and Therapeutics, Department of Molecular and Clinical Pharmacology, Institute of Translational Medicine, University of Liverpool, Liverpool, United Kingdom Astellas Pharma Global Development, Inc., Northbrook, Illinois, USA.

Astellas Pharma Global Development, Inc., Northbrook, Illinois, USA.

出版信息

Antimicrob Agents Chemother. 2016 Jul 22;60(8):4568-76. doi: 10.1128/AAC.00514-16. Print 2016 Aug.

Abstract

Isavuconazonium sulfate (Cresemba; Astellas Pharma Inc.), a water-soluble prodrug of the triazole antifungal agent isavuconazole, is available for the treatment of invasive aspergillosis (IA) and invasive mucormycosis. A population pharmacokinetic (PPK) model was constructed using nonparametric estimation to compare the pharmacokinetic (PK) behaviors of isavuconazole in patients treated in the phase 3 VITAL open-label clinical trial, which evaluated the efficacy and safety of the drug for treatment of renally impaired IA patients and patients with invasive fungal disease (IFD) caused by emerging molds, yeasts, and dimorphic fungi. Covariates examined were body mass index (BMI), weight, race, impact of estimated glomerular filtration rate (eGFR) on clearance (CL), and impact of weight on volume. PK parameters were compared based on IFD type and other patient characteristics. Simulations were performed to describe the MICs covered by the clinical dosing regimen. Concentrations (n = 458) from 136 patients were used to construct a 2-compartment model (first-order absorption compartment and central compartment). Weight-related covariates affected clearance, but eGFR did not. PK parameters and intersubject variability of CL were similar across different IFD groups and populations. Target attainment analyses demonstrated that the clinical dosing regimen would be sufficient for total drug area under the concentration-time curve (AUC)/MIC targets ranging from 50.5 for Aspergillus spp. (up to the CLSI MIC of 0.5 mg/liter) to 270 and 5,053 for Candida albicans (up to MICs of 0.125 and 0.004 mg/liter, respectively) and 312 for non-albicans Candida spp. (up to a MIC of 0.125 mg/liter). The estimations for Candida spp. were exploratory considering that no patients with Candida infections were included in the current analyses. (The VITAL trial is registered at ClinicalTrials.gov under number NCT00634049.).

摘要

硫酸艾沙康唑(Cresemba;安斯泰来制药公司)是三唑类抗真菌药艾沙康唑的水溶性前体药物,可用于治疗侵袭性曲霉病(IA)和侵袭性毛霉病。采用非参数估计构建群体药代动力学(PPK)模型,以比较在3期VITAL开放标签临床试验中接受治疗的患者体内艾沙康唑的药代动力学(PK)行为,该试验评估了该药治疗肾功能受损的IA患者以及由新出现的霉菌、酵母菌和双相真菌引起的侵袭性真菌病(IFD)患者的疗效和安全性。所考察的协变量包括体重指数(BMI)、体重、种族、估计肾小球滤过率(eGFR)对清除率(CL)的影响以及体重对血药浓度-时间曲线下面积(AUC)的影响。基于IFD类型和其他患者特征对PK参数进行比较。进行模拟以描述临床给药方案所覆盖的最低抑菌浓度(MIC)。使用136例患者的458个血药浓度数据构建二室模型(一级吸收室和中央室)。与体重相关的协变量影响清除率,但eGFR不影响。不同IFD组和人群的PK参数以及CL的个体间变异性相似。目标达成分析表明,临床给药方案对于浓度-时间曲线下总面积(AUC)/MIC目标范围是足够的,对于曲霉属(高达CLSI MIC为0.5 mg/L)为50.5,对于白色念珠菌(高达MIC分别为0.125和0.004 mg/L)为270和5053,对于非白色念珠菌属(高达MIC为0.125 mg/L)为312。考虑到当前分析中未纳入念珠菌感染患者,对念珠菌属的估计是探索性估计。(VITAL试验已在ClinicalTrials.gov上注册,注册号为NCT00634049。)

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d36/4958143/57aaa41b5672/zac0081653550001.jpg

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