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拓扑替康的群体药代动力学:总药物的个体内变异性。

Population pharmacokinetics of topotecan: intraindividual variability in total drug.

作者信息

Montazeri A, Boucaud M, Lokiec F, Pinguet F, Culine S, Déporte-Féty R, Albin N, Laguerre B, Goupil A, Bugat R, Canal P, Chatelut E

机构信息

Institut Claudius-Regaud, Toulouse, France.

出版信息

Cancer Chemother Pharmacol. 2000;46(5):375-81. doi: 10.1007/s002800000161.

Abstract

The inter- and intraindividual variabilities in topotecan clearance (CL) were explored using a population pharmacokinetic approach. Total (lactone + hydroxy acid) topotecan plasma concentrations were obtained in 31 women with metastatic epithelial ovarian cancer treated by the 30-min intravenous infusion on 5 subsequent days. The data corresponding to three occasions (days 1 and 5 of cycle 1, and day 1 of cycle 2), were analyzed using the nonlinear mixed effect model program. A large interindividual variability was observed, with CL varying from 9.1 to 42.51 per hour (mean 21.0). Topotecan CL was related to serum creatinine level, and age. A close relationship was also observed between topotecan CL and creatinine clearance. Intraindividual variability both within cycle 1 and between the two first cycles was limited, with a mean variation of -2+/-17%, and + 5+/-20%, respectively. A limited sampling strategy using Bayesian estimation based on two samples (5 min before the end of the 30-min infusion, and 4 h after the end of infusion) was developed. The results of this study combine relationships between topotecan pharmacokinetic parameters and patient covariates that may be useful for a priori dose adjustment, and convenient sampling procedure that can be used for further studies and drug monitoring.

摘要

采用群体药代动力学方法探讨了拓扑替康清除率(CL)的个体间和个体内变异性。对31例转移性上皮性卵巢癌女性患者进行研究,她们在随后5天内接受30分钟静脉输注治疗,测定了总(内酯+羟酸)拓扑替康血浆浓度。使用非线性混合效应模型程序分析了三个时间点(第1周期的第1天和第5天,以及第2周期的第1天)的数据。观察到较大的个体间变异性,CL范围为每小时9.1至42.51(平均21.0)。拓扑替康CL与血清肌酐水平和年龄有关。拓扑替康CL与肌酐清除率之间也观察到密切关系。第1周期内和两个初始周期之间的个体内变异性有限,平均变异分别为-2±17%和+5±20%。基于两个样本(30分钟输注结束前5分钟和输注结束后4小时)采用贝叶斯估计开发了一种有限采样策略。本研究结果结合了拓扑替康药代动力学参数与患者协变量之间的关系,这可能有助于先验剂量调整,以及可用于进一步研究和药物监测的便捷采样程序。

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