Efficacy of vedolizumab and ustekinumab in pediatric-onset inflammatory bowel disease: A real-world multicenter study.

IF 2.4 3区 医学 Q3 GASTROENTEROLOGY & HEPATOLOGY Journal of Pediatric Gastroenterology and Nutrition Pub Date : 2024-10-16 DOI:10.1002/jpn3.12384
Soleynne Rébus, Stéphanie Coopman, Djamal Djeddi, Audrey Vanrenterghem, Claire Dupont, Edouard Lacotte, Delphine Ley
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Abstract

Objectives: Vedolizumab and ustekinumab are effective in inducing and maintaining corticosteroid-free clinical remission (CFR) in adult patients with inflammatory bowel disease (IBD). This study describes the efficacy and safety of vedolizumab and ustekinumab in pediatric IBD.

Methods: All patients ≤18 years of age with Crohn's disease (CD) or ulcerative colitis (UC) treated with vedolizumab or ustekinumab in three centers in Northern France were followed retrospectively. The primary outcome was CFR at Week 14 (W14).

Results: Twenty-five patients (9 CD, 16 UC) and 33 patients (28 CD, 5 UC) were started on vedolizumab and ustekinumab respectively between 2016 and 2021. All were previously treated with antitumor necrosis factor (TNF). The median time from diagnosis to treatment initiation was 21.0 (12.0-44.0) and 42.0 (22.0-73.5) months for vedolizumab and ustekinumab respectively. Among vedolizumab-treated patients, 36% were in CFR at W14, including 22% in CD and 44% in UC. At W52, 56% were in CFR, including 33% in CD and 69% in UC. Among ustekinumab-treated patients, 49% were in CFR at W14, including 54% in CD and 20% in UC. At W52, 55% were in CFR, including 57% in CD and 40% in UC. There was a significant increase in median growth velocity between W0 and W52 of +2 SD in vedolizumab-treated patients (p = 0.0002). Four adverse events were reported during vedolizumab treatment, none for ustekinumab-treated patients.

Conclusions: Vedolizumab and ustekinumab appear to be effective in inducing and maintaining CFR in pediatric-onset IBD. Randomized controlled trials are needed to confirm these results.

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维多珠单抗和乌司替尼对儿科炎症性肠病的疗效:一项真实世界多中心研究。
目的:维多珠单抗和乌司替尼能有效诱导和维持成年炎症性肠病(IBD)患者的无皮质类固醇临床缓解(CFR)。本研究介绍了维多单抗和乌司替尼在小儿IBD中的疗效和安全性:方法:在法国北部的三个中心对所有年龄小于18岁的克罗恩病(CD)或溃疡性结肠炎(UC)患者使用维多珠单抗或乌司替尼进行了回顾性随访。主要结果是第14周(W14)的CFR:25名患者(9名CD患者,16名UC患者)和33名患者(28名CD患者,5名UC患者)分别于2016年至2021年间开始使用维多珠单抗和乌司替尼。所有患者之前都接受过抗肿瘤坏死因子(TNF)治疗。维多珠单抗和乌斯特库单抗从诊断到开始治疗的中位时间分别为21.0(12.0-44.0)个月和42.0(22.0-73.5)个月。在韦多珠单抗治疗的患者中,36%在W14时处于CFR状态,其中22%为CD患者,44%为UC患者。在 W52 期,56% 的患者处于 CFR 期,其中 CD 期为 33%,UC 期为 69%。在接受过乌司替尼治疗的患者中,49%在W14时处于CFR状态,包括54%的CD患者和20%的UC患者。在W52时,55%的患者处于CFR状态,包括57%的CD患者和40%的UC患者。在W0至W52期间,维多珠单抗治疗患者的中位生长速度明显增加了+2 SD(p = 0.0002)。韦多珠单抗治疗期间报告了四例不良事件,而乌司替尼治疗患者无不良事件报告:结论:维多利珠单抗和乌司替尼似乎能有效诱导和维持小儿IBD患者的CFR。需要进行随机对照试验来证实这些结果。
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来源期刊
CiteScore
5.30
自引率
13.80%
发文量
467
审稿时长
3-6 weeks
期刊介绍: ​The Journal of Pediatric Gastroenterology and Nutrition (JPGN) provides a forum for original papers and reviews dealing with pediatric gastroenterology and nutrition, including normal and abnormal functions of the alimentary tract and its associated organs, including the salivary glands, pancreas, gallbladder, and liver. Particular emphasis is on development and its relation to infant and childhood nutrition.
期刊最新文献
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