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Effectiveness and Safety of Ustekinumab in Pediatric Ulcerative Colitis: A Multi-center Retrospective Study from the Pediatric IBD Porto Group of ESPGHAN

Cohen, Shlomi; Rolandsdotter, Helena; Kolho, Kaija-Leena; Turner, Dan; Tzivinikos, Christos; Bramuzzo, Matteo; Pujol-Muncunill, Gemma; Scarallo, Luca; Urlep, Darja; Rinawi, Firas; Granot, Maya; Kang, Ben; Longueville, Ylva; Rodríguez-Belvís, Marta Velasco; Weintraub, Yael; Navas-López, Víctor Manuel; Yerushalmy-Feler, Anat (2024-05-23)

 
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s40272-024-00631-z-1.pdf (669.6Kt)
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Cohen, Shlomi
Rolandsdotter, Helena
Kolho, Kaija-Leena
Turner, Dan
Tzivinikos, Christos
Bramuzzo, Matteo
Pujol-Muncunill, Gemma
Scarallo, Luca
Urlep, Darja
Rinawi, Firas
Granot, Maya
Kang, Ben
Longueville, Ylva
Rodríguez-Belvís, Marta Velasco
Weintraub, Yael
Navas-López, Víctor Manuel
Yerushalmy-Feler, Anat
23.05.2024

Pediatric Drugs
doi:10.1007/s40272-024-00631-z
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Julkaisun pysyvä osoite on
https://urn.fi/URN:NBN:fi:tuni-202407097551

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Peer reviewed
Tiivistelmä
<p>Background and Objectives: Current data on ustekinumab therapy in children with ulcerative colitis (UC) or unclassified inflammatory bowel disease (IBDU) are limited. We aimed to evaluate the effectiveness and safety of ustekinumab in pediatric UC and IBDU. Methods: This multicenter retrospective study included 16 centers affiliated with the IBD Interest and Porto groups of ESPGHAN. Children with UC or IBDU treated with ustekinumab were enrolled. Demographic, clinical, laboratory, endoscopic, and imaging data as well as adverse events were recorded. Analyses were all based on the intention-to-treat principle. Results: Fifty-eight children (39 UC and 19 IBDU, median age 14.5 [IQR 11.5–16.5] years) were included. All had failed biologic therapies, and 38 (66%) had failed two or more biologics. Corticosteroid-free clinical remission (CFR) was observed in 27 (47%), 33 (57%), and 37 (64%) children at 16, 26, and 52 weeks, respectively. Normalization of C-reactive protein and calprotectin < 150 μg/g were achieved in 60% and 52%, respectively, by 52 weeks. Endoscopic and radiologic remissions were reached in 8% and 23%, respectively. The main predictors of CFR were diagnosis of UC compared with IBDU (hazard ratio [HR] 2.2, 95% CI 1.03–4.85; p = 0.041) and no prior vedolizumab therapy (HR 2.1, 95% CI 1.11–4.27; p = 0.023). Ustekinumab serum levels were not associated with disease activity. Adverse events were recorded in six (10%) children, leading to discontinuation of the drug in three. Conclusion: Based on these findings, ustekinumab appears as an effective therapy for pediatric refractory UC and IBDU. The potential efficacy should be weighed against the risks of serious adverse events.</p>
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  • TUNICRIS-julkaisut [20153]
Kalevantie 5
PL 617
33014 Tampereen yliopisto
oa[@]tuni.fi | Tietosuoja | Saavutettavuusseloste
 

 

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Kalevantie 5
PL 617
33014 Tampereen yliopisto
oa[@]tuni.fi | Tietosuoja | Saavutettavuusseloste