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群体药代动力学分析显示,阿瑞匹坦对异环磷酰胺、2-去氯异环磷酰胺和3-去氯异环磷酰胺的药代动力学没有影响。

Population pharmacokinetic analysis reveals no impact of aprepitant on the pharmacokinetics of ifosfamide, 2-dechloroifosfamide, and 3-dechloroifosfamide.

作者信息

Valentin Thibaud, Lambert Marie, Chaltiel Léonor, Allal Ben, Mseddi Mourad, Yakoubi Malika, Chevreau Christine, Toulmonde Maud, Firmin Nelly, Filleron Thomas, Chatelut Etienne

机构信息

Institut Claudius-Regaud, IUCT-Oncopole, Toulouse, France.

Institut Claudius-Regaud, IUCT-Oncopole, Toulouse, France; CRCT, Université de Toulouse, Inserm, France.

出版信息

Eur J Pharm Sci. 2023 Jun 1;185:106420. doi: 10.1016/j.ejps.2023.106420. Epub 2023 Mar 5.

Abstract

PURPOSE

Several case reports and retrospective series have clearly pointed to the role of aprepitant, an antiemetic drug, in the development of encephalopathy when used with ifosfamide. Described as an inhibitor of several CYP metabolic pathways, aprepitant is suspected of drug-drug-interaction on ifosfamide pharmacokinetics. The pharmacokinetics of ifosfamide and two of its metabolites (2-dechloroifosfamide and 3-dechloroifosfamide) was studied in patients with soft tissue sarcomas to evaluate the impact of aprepitant administration.

METHODS

A population pharmacokinetic approach was applied to analyze data obtained in 42 patients at cycle 1 (without aprepitant) and cycle 2 (with aprepitant for 34 of them).

RESULTS

A previously published pharmacokinetic model including a time-dependency process well fit the data. Aprepitant had no impact on ifosfamide or its two metabolite pharmacokinetic parameters.

CONCLUSION

This study suggests that aprepitant does not lead to a significant modification of ifosfamide metabolization, even though other metabolites such as 4 hydroxyifosfamide and chloroacetaldehyde were not monitored in this study.

摘要

目的

多项病例报告和回顾性系列研究已明确指出,抗呕吐药物阿瑞匹坦与异环磷酰胺联用时在脑病发展中所起的作用。阿瑞匹坦被描述为几种细胞色素P450(CYP)代谢途径的抑制剂,怀疑其对异环磷酰胺的药代动力学存在药物相互作用。本研究在软组织肉瘤患者中研究了异环磷酰胺及其两种代谢产物(2-去氯异环磷酰胺和3-去氯异环磷酰胺)的药代动力学,以评估阿瑞匹坦给药的影响。

方法

采用群体药代动力学方法分析42例患者在第1周期(未使用阿瑞匹坦)和第2周期(其中34例使用阿瑞匹坦)获得的数据。

结果

一个先前发表的包含时间依赖性过程的药代动力学模型很好地拟合了数据。阿瑞匹坦对异环磷酰胺或其两种代谢产物的药代动力学参数没有影响。

结论

本研究表明,即使本研究中未监测其他代谢产物如4-羟基异环磷酰胺和氯乙醛,阿瑞匹坦也不会导致异环磷酰胺代谢的显著改变。

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