甲氨蝶呤临床相互作用的重要回顾:转运蛋白的作用。

IF 3.9 3区 医学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Expert Opinion on Drug Metabolism & Toxicology Pub Date : 2023-02-01 DOI:10.1080/17425255.2023.2193325
Fatemeh Jafari, Omid Arasteh, Hesamoddin Hosseinjani, Abolghasem Allahyari, Sajad Ataei Azimi, Vahid Reza Askari
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引用次数: 0

摘要

简介:甲氨蝶呤(MTX)是一种抗叶酸和免疫抑制药物,用于各种恶性肿瘤和免疫疾病。然而,与同时使用某些药物相关的MTX的延迟消除可能导致严重和危及生命的不良反应。涉及领域:本文研究了药物与MTX相互作用导致MTX水平升高,以及由于转运体的作用而产生的相关不良反应。甲氨蝶呤的毒性在低剂量和高剂量均有发生。根据我们回顾的研究,大多数与甲氨喋呤的相互作用记录发生在吲哚美辛、酮洛芬、奥美拉唑、哌拉西林/他唑巴坦、环丙沙星、复方新诺明、probenecid和伊马替尼共同给药时,主要是由于转运体的作用。然而,大多数研究都是病例报告或系列研究,确切的药物与甲氨蝶呤相互作用还需要进一步的临床研究。专家意见:我们的研究结果显示,没有确凿的证据表明质子泵抑制剂(PPIs)、左乙拉西坦和非甾体抗炎药与甲氨蝶呤相互作用。低白蛋白血症、肾功能衰竭、第三空间液体潴留、老年人、多药、转运抑制是MTX毒性的最关键因素。如果替代或暂时停药是不可能的,医疗保健提供者应该意识到相互作用,特别是对有MTX毒性危险因素的患者。
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A critical review of methotrexate clinical interactions: role of transporters.

Introduction: Methotrexate (MTX) is an antifolate and immunosuppressive drug prescribed for various malignancies and immune diseases. However, delayed elimination of MTX associated with concomitant use of some medications can lead to severe and lifethreatening adverse effects.

Areas covered: This paper investigated drugMTX interactions that lead to elevated MTX levels and related adverse effects due to the role of transporters. Methotrexate toxicity occurs at both low and high doses administrations. According to the studies we reviewed in this paper, most interaction records with methotrexate occurred with coadministration of indomethacin, ketoprofen, omeprazole, piperacillin/tazobactam, ciprofloxacin, cotrimoxazole, probenecid, and imatinib, mainly due to the role of transporters. However, most studies were performed as case reports or series, and confirming the exact drugmethotrexate interaction still needs further clinical investigations.

Expert opinion: Our findings showed no firm evidence of interactions of proton pump inhibitors (PPIs), levetiracetam, and NSAIDS with MTX. Moreover, patients' risk factors, hypoalbuminemia, renal failure, third space fluid retention, the elderly, polypharmacy, and transport inhibition are the most critical factors for MTX toxicity. If substitution or temporary discontinuation is not possible, healthcare providers should be aware of interactions, especially in patients with risk factors for MTX toxicity.

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来源期刊
Expert Opinion on Drug Metabolism & Toxicology
Expert Opinion on Drug Metabolism & Toxicology 医学-生化与分子生物学
CiteScore
7.90
自引率
2.30%
发文量
62
审稿时长
4-8 weeks
期刊介绍: Expert Opinion on Drug Metabolism & Toxicology (ISSN 1742-5255 [print], 1744-7607 [electronic]) is a MEDLINE-indexed, peer-reviewed, international journal publishing review articles on all aspects of ADME-Tox. Each article is structured to incorporate the author’s own expert opinion on the scope for future development. The Editors welcome: Reviews covering metabolic, pharmacokinetic and toxicological issues relating to specific drugs, drug-drug interactions, drug classes or their use in specific populations; issues relating to enzymes involved in the metabolism, disposition and excretion of drugs; techniques involved in the study of drug metabolism and toxicology; novel technologies for obtaining ADME-Tox data. Drug Evaluations reviewing the clinical, toxicological and pharmacokinetic data on a particular drug. The audience consists of scientists and managers in the pharmaceutical industry, pharmacologists, clinical toxicologists and related professionals.
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