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甲氨蝶呤相关不良事件以及叶酸与肿瘤坏死因子-α抑制剂联合治疗的影响:使用美国食品药品监督管理局不良事件报告系统进行的评估

Methotrexate-related adverse events and impact of concomitant treatment with folic acid and tumor necrosis factor-alpha inhibitors: An assessment using the FDA adverse event reporting system.

作者信息

Onda Kenji, Honma Takeshi, Masuyama Koichi

机构信息

Department of Clinical Pharmacology, School of Pharmacy, Tokyo University of Pharmacy and Life Sciences, Tokyo, Japan.

Bohsei Pharmacy, Kanagawa, Japan.

出版信息

Front Pharmacol. 2023 Feb 22;14:1030832. doi: 10.3389/fphar.2023.1030832. eCollection 2023.

Abstract

Methotrexate (MTX) is an essential anti-rheumatic drug used to treat rheumatoid arthritis (RA). Prevention or management of adverse reactions, including interstitial lung disease (ILD), hepatotoxicity, myelosuppression, and infection, remains fundamental for safe MTX therapy. Using the Food and Drug Administration (FDA) Adverse Event Reporting System (FAERS) (JAPIC AERS), we performed disproportionality analyses of adverse events related to MTX use and the impact of concomitant medications. Upon analyzing all reported cases in FAERS between 1997 and 2019, the crude reporting odds ratios (cRORs; 95% confidence intervals) for ILD, hepatotoxicity, myelosuppression, and tuberculosis (TB) in relation to MTX use were 4.00 (3.83-4.17), 1.99 (1.96-2.02), 3.66 (3.58-3.74), and 7.97 (7.65-8.3), respectively. Combining MTX with folic acid (FA) or tumor necrosis factor-alpha inhibitors (TNFis) tended to reduce cRORs for these adverse events (except for TB). Multiple logistic regression analysis in patients with RA was conducted to calculate adjusted reporting odds ratios (aRORs) for age, sex, and MTX treatment patterns (MTX alone and combined with FA and TNFi). Higher age (except for hepatotoxicity) and male sex were significantly associated with adverse events. Combining FA or TNFi with MTX reduced aRORs for MTX-related hepatotoxicity and myelosuppression; in contrast, the effect of FA was not obvious in ILD or TB. Although studies assessing spontaneous reporting systems have limitations such as reporting bias, data from our logistic regression analysis demonstrated that adding FA to MTX-based therapy could help reduce the dose-dependent adverse events of MTX, thereby providing clinical evidence that supports the beneficial effect of FA. This study also demonstrated the usefulness of FAERS in comparing adverse events based on treatment patterns.

摘要

甲氨蝶呤(MTX)是用于治疗类风湿关节炎(RA)的一种重要抗风湿药物。预防或处理包括间质性肺疾病(ILD)、肝毒性、骨髓抑制和感染在内的不良反应,仍然是MTX安全治疗的根本。我们使用美国食品药品监督管理局(FDA)不良事件报告系统(FAERS)(日本药品不良反应报告系统(JAPIC AERS)),对与MTX使用相关的不良事件以及合并用药的影响进行了不成比例分析。在分析1997年至2019年FAERS中所有报告病例后,与MTX使用相关的ILD、肝毒性、骨髓抑制和结核病(TB)的粗报告比值比(cRORs;95%置信区间)分别为4.00(3.83 - 4.17)、1.99(1.96 - 2.02)、3.66(3.58 - 3.74)和7.97(7.65 - 8.3)。将MTX与叶酸(FA)或肿瘤坏死因子-α抑制剂(TNFis)联合使用往往会降低这些不良事件的cRORs(结核病除外)。我们对类风湿关节炎患者进行了多因素逻辑回归分析,以计算年龄、性别和MTX治疗模式(单独使用MTX以及与FA和TNFi联合使用)的调整报告比值比(aRORs)。较高年龄(肝毒性除外)和男性与不良事件显著相关。将FA或TNFi与MTX联合使用可降低MTX相关肝毒性和骨髓抑制的aRORs;相比之下,FA对ILD或TB的影响不明显。尽管评估自发报告系统的研究存在报告偏倚等局限性,但我们逻辑回归分析的数据表明,在基于MTX的治疗中添加FA有助于减少MTX的剂量依赖性不良事件,从而提供了支持FA有益作用的临床证据。本研究还证明了FAERS在基于治疗模式比较不良事件方面的有用性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25fa/9992735/ed9f8eaca46b/fphar-14-1030832-g001.jpg

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