Anti-Tumor Necrosis Factor-α Use in Pediatric Inflammatory Bowel Disease-Reports from a Romanian Center.

IF 4.8 3区 医学 Q2 CHEMISTRY, MEDICINAL Pharmaceuticals Pub Date : 2025-01-11 DOI:10.3390/ph18010084
Roxana Matran, Andra-Mihaela Diaconu, Andreea Maria Iordache, Irina Dijmărescu, Alexandra Coroleucă, Daniela Păcurar, Cristina Becheanu
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Abstract

Background/Objectives: The introduction of anti-tumor necrosis factor-α (anti-TNF-α) agents, particularly infliximab (IFX) and adalimumab (ADA), has significantly expanded the therapeutic arsenal for inflammatory bowel disease (IBD). While these biologics have demonstrated substantial efficacy, they are associated with a spectrum of potential adverse events (AEs). This study aims to evaluate and document these AEs to facilitate optimal patient selection and monitoring strategies of patients undergoing these therapies. Methods: This retrospective, single-center study examined pediatric IBD patients receiving anti-TNF-α therapy at the "Grigore Alexandrescu" Emergency Hospital for Children in Bucharest, Romania, from January 2015 to October 2024. AEs were categorized into non-infectious complications (acute infusion reactions, anti-drug antibody formation), dermatological effects (erythema nodosum, vasculitis), neurological effects (Guillain-Barré syndrome), and infections. AEs were analyzed in relation to the specific anti-TNF-α agent administered and comprehensively characterized. Results: Of 40 patients enrolled, 22 (55%) had Crohn's disease (CD). The median (IQR) age at diagnosis was 14.8 years [10.8-15.9]. IFX was used in 34 (85%) patients while 6 (15%) patients received either ADA or IFX/ADA sequential therapy. Twenty-seven AEs were documented in 19 (47.5%) patients, the most prevalent being antidrug antibody formation (44.4%), infections (22.2%), and acute infusion reactions (22.2%). All ADA-exposed patients experienced at least one AE, compared to 41.2% (n = 14) patients treated with IFX, p = 0.01. Conclusions: AEs were observed in approximately half of the study cohort, with anti-drug antibody formation emerging as the most frequent complication. ADA therapy was associated with a significantly higher rate of AEs compared to IFX. These findings underscore the critical importance of vigilant monitoring for patients undergoing anti-TNF-α therapy in pediatric IBD management.

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抗肿瘤坏死因子-α在儿童炎症性肠病中的应用——来自罗马尼亚中心的报告
背景/目的:抗肿瘤坏死因子-α (anti-TNF-α)药物的引入,特别是英夫利昔单抗(IFX)和阿达木单抗(ADA),显著扩大了炎症性肠病(IBD)的治疗药库。虽然这些生物制剂已经证明了实质性的疗效,但它们与一系列潜在的不良事件(ae)有关。本研究旨在评估和记录这些不良事件,以促进患者的最佳选择和患者接受这些治疗的监测策略。方法:这项回顾性单中心研究调查了2015年1月至2024年10月在罗马尼亚布加勒斯特“Grigore Alexandrescu”儿童急救医院接受抗tnf -α治疗的儿童IBD患者。ae分为非感染性并发症(急性输注反应、抗药物抗体形成)、皮肤病效应(结节性红斑、血管炎)、神经系统效应(格林-巴罗综合征)和感染。分析ae与给药的特异性抗tnf -α药物的关系,并对ae进行综合表征。结果:入组的40例患者中,22例(55%)患有克罗恩病(CD)。诊断时的中位(IQR)年龄为14.8岁[10.8-15.9]。34例(85%)患者使用IFX, 6例(15%)患者接受ADA或IFX/ADA序贯治疗。19例(47.5%)患者发生27例不良反应,最常见的是抗药抗体形成(44.4%)、感染(22.2%)和急性输液反应(22.2%)。与使用IFX治疗的41.2% (n = 14)患者相比,所有暴露于ada的患者至少经历一次AE, p = 0.01。结论:在大约一半的研究队列中观察到ae,抗药物抗体形成是最常见的并发症。与IFX相比,ADA治疗与更高的不良事件发生率相关。这些发现强调了在儿童IBD治疗中对接受抗tnf -α治疗的患者进行警惕监测的重要性。
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来源期刊
Pharmaceuticals
Pharmaceuticals Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
6.10
自引率
4.30%
发文量
1332
审稿时长
6 weeks
期刊介绍: Pharmaceuticals (ISSN 1424-8247) is an international scientific journal of medicinal chemistry and related drug sciences.Our aim is to publish updated reviews as well as research articles with comprehensive theoretical and experimental details. Short communications are also accepted; therefore, there is no restriction on the maximum length of the papers.
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