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低剂量培美曲塞药代动力学的预测:一项概念验证研究。

Prediction of the pharmacokinetics of pemetrexed with a low test dose: A proof-of-concept study.

作者信息

Boosman René J, de Rouw Nikki, Huitema Alwin D R, Burgers Jacobus A, Ter Heine Rob

机构信息

Department of Pharmacy & Pharmacology, Antoni van Leeuwenhoek - The Netherlands Cancer Institute, Amsterdam, the Netherlands.

Department of Pharmacy, Radboud Institute for Health Sciences, Radboud University Medical Center, Nijmegen, the Netherlands.

出版信息

Br J Clin Pharmacol. 2023 Feb;89(2):699-704. doi: 10.1111/bcp.15520. Epub 2022 Sep 21.

Abstract

PURPOSE

Pemetrexed is a cytotoxic drug used for the treatment of lung cancer and mesothelioma. The use of a low test dosing of cytotoxic drugs may aid in dose individualization without causing harm. The aim of this proof-of-concept study was to assess if the pharmacokinetics (PKs) of a test dose could predict the PKs of a therapeutic pemetrexed dose.

METHODS

Ten patients received both a low test dose (100 μg) and a therapeutic dose of pemetrexed after which plasma concentrations pemetrexed were measured. PK analysis was performed by means of nonlinear mixed-effects modelling. The predictive performances of test dose clearance and renal function towards a therapeutic dose were assessed.

RESULTS

The PKs of a pemetrexed test dose were best described by a one-compartment model with linear elimination. A high variability in the administered dose was observed for the test dose, but not for the therapeutic dose. A statistically significant correlation between test dose clearance and therapeutic dose clearance was observed (Spearman's rho: 0.758, P = 0.02). The predictive performance of test dose clearance was worse than renal function: mean predictive error (+95% confidence interval [CI]) 53.9% (50.1-57.6%) vs 19.4% (12.4-26.4%) and normalized root-mean square error (+95% CI) 57.8% (30.5-85.1%) vs 25.7% (20.3-31.0%).

CONCLUSION

We show that test dosing of pemetrexed is feasible, but there seems no added value for a low test dosing in the dose individualization of pemetrexed.

摘要

目的

培美曲塞是一种用于治疗肺癌和间皮瘤的细胞毒性药物。使用低剂量的细胞毒性药物进行试验性给药可能有助于实现剂量个体化且不会造成伤害。本概念验证研究的目的是评估试验剂量的药代动力学(PKs)是否能够预测治疗剂量培美曲塞的PKs。

方法

10名患者接受了低试验剂量(100μg)和治疗剂量的培美曲塞,之后测量培美曲塞的血浆浓度。通过非线性混合效应模型进行PK分析。评估试验剂量清除率和肾功能对治疗剂量的预测性能。

结果

培美曲塞试验剂量的PKs最好用具有线性消除的单室模型来描述。试验剂量的给药剂量存在高变异性,但治疗剂量不存在。观察到试验剂量清除率与治疗剂量清除率之间存在统计学显著相关性(Spearman秩相关系数:0.758,P = 0.02)。试验剂量清除率的预测性能比肾功能差:平均预测误差(+95%置信区间[CI])为53.9%(50.1 - 57.6%),而肾功能为19.4%(12.4 - 26.4%);归一化均方根误差(+95%CI)为57.8%(30.5 - 85.1%),而肾功能为25.7%(20.3 - 31.0%)。

结论

我们表明培美曲塞试验性给药是可行的,但在培美曲塞的剂量个体化中,低试验剂量似乎没有额外价值。

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