Population pharmacokinetics of cisplatin in Asian Indian cancer patients

Harish K. Kaushik, Vijay Kumar, Satish B. Kumar, N. Reddy, V. K. Raghavaiah, K. Devarakonda
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引用次数: 3

Abstract

The aim of this study was to describe population pharmacokinetics of cisplatin in an Indian cancer population. Dosage adjustment based on individual pharmacokinetic parameters is of considerable importance for effective and safe use of drugs. Extensive work on cisplatin and other was carried out in different cancer patient populations, but no data are available in Indian cancer patients. In the present study 154 steady state concentrations of cisplatin were analyzed from 46 patients. Pharmacostatistical work was done by using NONMEM. The covariates evaluated in this study were age, body weight, height, sex, and creatinine clearance. The model found to best describe the data following the FO and FOCE method was: Clearance (CL) = θ1*(CLCR/74.92) *EXP (η1) and Volume (V) = {θ2 *(AGE/52.3) + θ3*(BSA/1.55)}*EXP (η2). The final model estimates of CL and V estimated by FO method were 3.02 L/h and 2.72 L, respectively, and by FOCE method were 3.39 L/h and 4.48 L, respectively. These parameters are utilized for individualizing the loading and maintenance doses in pediatric patients.
顺铂在亚洲印度癌症患者中的人群药代动力学
本研究的目的是描述顺铂在印度癌症人群中的群体药代动力学。基于个体药代动力学参数的剂量调整对于药物的有效和安全使用具有相当重要的意义。在不同的癌症患者群体中进行了大量关于顺铂和其他药物的研究,但没有关于印度癌症患者的数据。本研究分析了46例患者的154例稳态顺铂浓度。采用NONMEM进行药物统计工作。本研究评估的协变量为年龄、体重、身高、性别和肌酐清除率。根据FO和FOCE方法发现的最能描述数据的模型为:Clearance (CL) = θ1*(CLCR/74.92) *EXP (η1), Volume (V) = {θ2 *(AGE/52.3) + θ3*(BSA/1.55)}*EXP (η2)。FO法估算的CL和V最终模型估计值分别为3.02 L/h和2.72 L, FOCE法估算的CL和V最终模型估计值分别为3.39 L/h和4.48 L。这些参数用于个性化儿科患者的负荷和维持剂量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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