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Article

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

by
Roxana Matran
1,2,
Andra-Mihaela Diaconu
2,*,
Andreea Maria Iordache
2,
Irina Dijmărescu
1,2,
Alexandra Coroleucă
1,2,
Daniela Păcurar
1,2 and
Cristina Becheanu
1,2
1
Department of Paediatrics, “Carol Davila” University of Medicine and Pharmacy, 050474 Bucharest, Romania
2
“Grigore Alexandrescu” Emergency Hospital for Children, 011743 Bucharest, Romania
*
Author to whom correspondence should be addressed.
Pharmaceuticals 2025, 18(1), 84; https://doi.org/10.3390/ph18010084
Submission received: 7 December 2024 / Revised: 7 January 2025 / Accepted: 8 January 2025 / Published: 11 January 2025
(This article belongs to the Section Pharmacology)

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.
Keywords: inflammatory bowel disease; anti-TNF-α; antidrug antibodies; acute-infusion reactions; adverse events inflammatory bowel disease; anti-TNF-α; antidrug antibodies; acute-infusion reactions; adverse events

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MDPI and ACS Style

Matran, R.; Diaconu, A.-M.; Iordache, A.M.; Dijmărescu, I.; Coroleucă, A.; Păcurar, D.; Becheanu, C. Anti-Tumor Necrosis Factor-α Use in Pediatric Inflammatory Bowel Disease—Reports from a Romanian Center. Pharmaceuticals 2025, 18, 84. https://doi.org/10.3390/ph18010084

AMA Style

Matran R, Diaconu A-M, Iordache AM, Dijmărescu I, Coroleucă A, Păcurar D, Becheanu C. Anti-Tumor Necrosis Factor-α Use in Pediatric Inflammatory Bowel Disease—Reports from a Romanian Center. Pharmaceuticals. 2025; 18(1):84. https://doi.org/10.3390/ph18010084

Chicago/Turabian Style

Matran, Roxana, Andra-Mihaela Diaconu, Andreea Maria Iordache, Irina Dijmărescu, Alexandra Coroleucă, Daniela Păcurar, and Cristina Becheanu. 2025. "Anti-Tumor Necrosis Factor-α Use in Pediatric Inflammatory Bowel Disease—Reports from a Romanian Center" Pharmaceuticals 18, no. 1: 84. https://doi.org/10.3390/ph18010084

APA Style

Matran, R., Diaconu, A.-M., Iordache, A. M., Dijmărescu, I., Coroleucă, A., Păcurar, D., & Becheanu, C. (2025). Anti-Tumor Necrosis Factor-α Use in Pediatric Inflammatory Bowel Disease—Reports from a Romanian Center. Pharmaceuticals, 18(1), 84. https://doi.org/10.3390/ph18010084

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