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Effectiveness and Safety of Biosimilars in Pediatric Non-infectious Uveitis: Real-Life Data from the International AIDA Network Uveitis Registry

Authors :
Maria Tarsia
Antonio Vitale
Carla Gaggiano
Jurgen Sota
Anna Maselli
Chiara Bellantonio
Silvana Guerriero
Rosanna Dammacco
Francesco La Torre
Gaafar Ragab
Mohamed Tharwat Hegazy
Alex Fonollosa
Maria Pia Paroli
Emanuela Del Giudice
Maria Cristina Maggio
Marco Cattalini
Lampros Fotis
Giovanni Conti
Angela Mauro
Adele Civino
Federico Diomeda
Alejandra de-la-Torre
Carlos Cifuentes-González
Samar Tharwat
José Hernández-Rodríguez
Verónica Gómez-Caverzaschi
Laura Pelegrín
Kalpana Babu
Vishali Gupta
Francesca Minoia
Piero Ruscitti
Stefania Costi
Luciana Breda
Saverio La Bella
Alessandro Conforti
Maria Antonietta Mazzei
Ester Carreño
Rana Hussein Amin
Salvatore Grosso
Bruno Frediani
Gian Marco Tosi
Alberto Balistreri
Luca Cantarini
Claudia Fabiani
Source :
Ophthalmology and Therapy, Vol 13, Iss 3, Pp 761-774 (2024)
Publication Year :
2024
Publisher :
Adis, Springer Healthcare, 2024.

Abstract

Abstract Introduction Since many biological drug patents have expired, biosimilar agents (BIOs) have been developed; however, there are still some reservations in their use, especially in childhood. The aim of the current study is to evaluate the efficacy and safety of tumor necrosis factor (TNF) inhibitors BIOs as treatment for pediatric non-infectious uveitis (NIU). Methods Data from pediatric patients with NIU treated with TNF inhibitors BIOs were drawn from the international AutoInflammatory Disease Alliance (AIDA) registries dedicated to uveitis and Behçet's disease. The effectiveness and safety of BIOs were assessed in terms of frequency of relapses, risk for developing ocular flares, best-corrected visual acuity (BCVA), glucocorticoids (GCs)-sparing effect, drug survival, frequency of ocular complications, and adverse drug event (AE). Results Forty-seven patients (77 affected eyes) were enrolled. The BIOs employed were adalimumab (ADA) (89.4%), etanercept (ETA) (5.3%), and infliximab (IFX) (5.3%). The number of relapses 12 months prior to BIOs and at last follow-up was 282.14 and 52.43 per 100 patients/year. The relative risk of developing ocular flares before BIOs introduction compared to the period following the start of BIOs was 4.49 (95% confidence interval [CI] 3.38–5.98, p = 0.004). The number needed to treat (NNT) for ocular flares was 3.53. Median BCVA was maintained during the whole BIOs treatment (p = 0.92). A significant GCs-sparing effect was observed throughout the treatment period (p = 0.002). The estimated drug retention rate (DRR) at 12-, 24-, and 36-month follow-up were 92.7, 83.3, and 70.8%, respectively. The risk rate for developing structural ocular complications was 89.9/100 patients/year before starting BIOs and 12.7/100 patients/year during BIOs treatment, with a risk ratio of new ocular complications without BIOs of 7.1 (CI 3.4–14.9, p = 0.0003). Three minor AEs were reported. Conclusions TNF inhibitors BIOs are effective in reducing the number of ocular uveitis relapses, preserving visual acuity, allowing a significant GCs-sparing effect, and preventing structural ocular complications. Trial Registration ClinicalTrials.gov ID NCT05200715.

Details

Language :
English
ISSN :
21938245 and 21936528
Volume :
13
Issue :
3
Database :
Directory of Open Access Journals
Journal :
Ophthalmology and Therapy
Publication Type :
Academic Journal
Accession number :
edsdoj.36a238cc1f34df1a1e80fe3d71aa6f8
Document Type :
article
Full Text :
https://doi.org/10.1007/s40123-023-00863-1