大剂量甲氨蝶呤输注的剂量预测。第一部分:经典试验剂量方案的评价。

J P Cano, R Bruno, N Lena, R Favre, A Iliadis, A M Imbert
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引用次数: 12

摘要

静脉注射(试验剂量)后的甲氨蝶呤(MTX)动力学初步评估允许个体化高剂量输注(HD-MTX)。该方法与治疗药物监测相结合,在17至650 mg/h给药的预测稳态水平(Css)(24至36小时内10(-5)至10(-4)M)的大范围内具有良好的性能(均方根误差:rmse (precision) = 1.54 X 10(-5) M(21.4%),平均误差:me (bias) = 0.043 X 10(-5) M (NS))。然而,在5 × 10(-4) M预测css8小时(970至1970 mg/h给药)时,出现了显著(p < 0.05)但相当低的剂量高估(me = 7.38 × 10(-5) M(14.8%))与预测精度下降(rmse = 13.3 × 10(-5) M(26.6%))相关的预测精度下降。然而,在许多情况下(29例中有6例),与预测的Css发生了重大偏差,这意味着需要在8小时前停止输注。这些结果表明,MTX的药代动力学从低试验剂量的丸入到高剂量的输注是线性的。这使得基于MTX清除率的初步估计和与输注期间和之后的治疗药物监测相关的剂量预测成为可能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Dosage predictions in high-dose methotrexate infusions. Part 1: Evaluation of the classic test-dose protocol.

A preliminary methotrexate (MTX) kinetic evaluation following administration of an IV bolus (test-dose) allowed individualization of high-dose infusions (HD-MTX). This approach combined with therapeutic drug monitoring was found to have good performance over a large scale of predicted steady-state levels (Css) (10(-5) to 10(-4) M over 24 to 36 h) corresponding to 17 to 650 mg/h deliveries (root mean squared error : rmse (precision) = 1.54 X 10(-5) M (21.4%) and mean error : me (bias) = 0.043 X 10(-5) M (NS)). However a significative (p less than 0.05) but rather low over-estimation of dosage (me = 7.38 X 10(-5) M (14.8%)) associated to a decrease in the prediction precision (rmse = 13.3 X 10(-5) M (26.6%)) occurred in 5 X 10(-4) M predicted Css over 8 h (970 to 1970 mg/h deliveries). However in a number of cases (6 out of 29) important deviations from predicted Css occurred, implying the need to stop the infusion before 8 h. These results indicated that MTX pharmacokinetics was linear from low test-dose bolus injections to high-dose infusions. This allowed dosage predictions based upon preliminary estimation of MTX clearance and associated to therapeutic drug monitoring during and following infusion.

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