Department of Clinical Pharmacy, The First Affiliated Hospital of Shandong First Medical University & Shandong Provincial Qianfoshan Hospital, Shandong Pediatric Drug Clinical Evaluation and R&D Research Center of Engineering Technology, Jinan, 250014, China.
Sci Rep. 2024 Aug 31;14(1):20288. doi: 10.1038/s41598-024-70955-w.
To establish a population pharmacokinetic (PopPK) model of posaconazole suspension in Chinese hematopoietic stem cell transplantation (HSCT) patients and to recommend an optimal dosing regimen. A single-center, retrospective, model-based study was conducted in 62 Chinese patients, including 103 with posaconazole plasma concentrations. PopPK analysis using NONMEM software. A one-compartment model of first-order elimination and absorption was in good agreement with the experimental data. Analysis of covariance showed that body weight (WT), creatinine clearance (CCR), and proton pump inhibitor (PPI) had a significant effect on the pharmacokinetics of posaconazole. The dose simulation results show that patients with CCR ≥ 90 mL/min require at least 3 mg/kg TID and 7 mg/kg BID dosing regimens for prevention and treatment, respectively. However, when combined with PPI, at least 5 mg/kg BID and 5 mg/kg TID dosing regimens are required for prevention and treatment, respectively. Regardless of whether it is used in combination with PPI or not, patients with a CCR of 60-90 mL/min can achieve PTA goals by using a 4 mg/kg BID and 4 mg/kg TID regimen for prevention and treatment, respectively. A dosing regimen of 3 mg/kg BID in patients with a CCR of 30-60 mL/min is sufficient to meet the PTA goal of prophylaxis, and the dose needs to be elevated to 4 mg/kg BID for the treatment of fungal infections, and there is no need to change the dose according to the coadministration of PPI. When the patient's CCR is less than 30 mL/min, whether or not combined with PPI, the administration regimen of 2 mg/kg BID and 3 mg/kg BID can meet the PTA goals for prevention and treatment, respectively.
建立中国造血干细胞移植(HSCT)患者泊沙康唑混悬液的群体药代动力学(PopPK)模型,并推荐最佳给药方案。这是一项在中国 62 例患者中进行的单中心、回顾性、基于模型的研究,其中 103 例患者有泊沙康唑血药浓度数据。使用 NONMEM 软件进行 PopPK 分析。泊沙康唑的药代动力学符合一室模型和一级吸收消除模型。协方差分析显示体重(WT)、肌酐清除率(CCR)和质子泵抑制剂(PPI)对泊沙康唑的药代动力学有显著影响。剂量模拟结果表明,CCR≥90 mL/min 的患者预防和治疗时至少需要 3 mg/kg TID 和 7 mg/kg BID 给药方案。但与 PPI 合用,预防和治疗时至少需要 5 mg/kg BID 和 5 mg/kg TID 给药方案。无论是否与 PPI 合用,CCR 为 60-90 mL/min 的患者预防和治疗时分别使用 4 mg/kg BID 和 4 mg/kg TID 方案可达到 PTA 目标。CCR 为 30-60 mL/min 的患者预防时使用 3 mg/kg BID 剂量即可满足 PTA 目标,治疗时需要提高剂量至 4 mg/kg BID,真菌感染时无需根据合用 PPI 调整剂量。当患者的 CCR 小于 30 mL/min 时,无论是否合用 PPI,给药方案分别为 2 mg/kg BID 和 3 mg/kg BID 即可满足预防和治疗的 PTA 目标。