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一项关于甲氨蝶呤与质子泵抑制剂或阿司匹林之间相互作用的非干预性回顾性队列研究。

A non-interventional retrospective cohort study of the interaction between methotrexate and proton pump inhibitors or aspirin.

作者信息

Boerrigter E, Crul M

机构信息

Division of Clinical Pharmacy, OLVG, Oosterpark 9, 1090HM Amsterdam, Netherlands.

Division of Clinical Pharmacy, OLVG, Oosterpark 9, 1090HM Amsterdam, Netherlands.

出版信息

Ann Pharm Fr. 2017 Sep;75(5):344-348. doi: 10.1016/j.pharma.2017.06.002. Epub 2017 Jul 10.

Abstract

INTRODUCTION

Methotrexate (MTX) is an antifolate drug, which is frequently used in the treatment of cancer. Proton pump inhibitors (PPIs) could delay the elimination of plasma MTX in high-dose MTX therapy by inhibition of tubular secretion, which could lead to MTX toxicity. However, the evidence of the clinical relevance of this drug-drug interaction is inconsistent. No previous studies into the effect of low dose aspirin on the elimination of MTX in high-dose therapy have been performed. Therefore, we evaluated the interaction between MTX and PPIs or aspirin.

METHODS

We conducted a non-interventional retrospective cohort study in patients treated with high dose MTX (≥500mg/m or >1000mg), between 2009 and 2016 at the OLVG ("Onze Lieve Vrouwe Gasthuis, Oost") in Amsterdam, the Netherlands. Patients were included if MTX concentrations were determined at 24, 48 or 72hours after high dose MTX treatment. We categorised the cycles of high dose MTX therapy into delayed elimination or normal elimination. Differences in patient characteristics and MTX dosing regimen were compared between all groups by X2-test, Fisher's exact probability test or Mann-Whitney U-test.

RESULTS

In total, 89 high dose MTX cycles were included. Delayed MTX elimination was observed in 27 (30.3%) cycles. Co-administration of a PPI was significantly more frequent in the delayed elimination group than in the normal elimination group (P<0.001). There was no statistical effect observed by co-administration of aspirin.

CONCLUSION

The use of PPIs during high dose MTX treatment can lead to delayed MTX elimination. Discontinuation of PPIs during high dose MTX treatment is recommended. Co-administration of aspirin did not influence the elimination of MTX, but further research is needed.

摘要

引言

甲氨蝶呤(MTX)是一种抗叶酸药物,常用于癌症治疗。质子泵抑制剂(PPIs)可通过抑制肾小管分泌来延缓高剂量MTX治疗中血浆MTX的消除,这可能导致MTX毒性。然而,这种药物相互作用的临床相关性证据并不一致。此前尚未有关于低剂量阿司匹林对高剂量治疗中MTX消除影响的研究。因此,我们评估了MTX与PPIs或阿司匹林之间的相互作用。

方法

我们在2009年至2016年期间,于荷兰阿姆斯特丹的OLVG(“Onze Lieve Vrouwe Gasthuis, Oost”)对接受高剂量MTX(≥500mg/m²或>1000mg)治疗的患者进行了一项非干预性回顾性队列研究。如果在高剂量MTX治疗后24、48或72小时测定了MTX浓度,则纳入患者。我们将高剂量MTX治疗周期分为消除延迟或正常消除。通过X²检验、Fisher精确概率检验或Mann-Whitney U检验比较所有组之间患者特征和MTX给药方案的差异。

结果

总共纳入了89个高剂量MTX周期。在27个(30.3%)周期中观察到MTX消除延迟。与正常消除组相比,延迟消除组中PPI的联合使用明显更频繁(P<0.001)。阿司匹林联合使用未观察到统计学效应。

结论

高剂量MTX治疗期间使用PPIs可导致MTX消除延迟。建议在高剂量MTX治疗期间停用PPIs。阿司匹林联合使用不影响MTX的消除,但需要进一步研究。

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