Rébus Soleynne, Coopman Stéphanie, Djeddi Djamal, Vanrenterghem Audrey, Dupont Claire, Lacotte Edouard, Ley Delphine
Department of Pediatrics, Division of Gastroenterology, Hepatology and Nutrition, CHU Lille, Lille, France.
Department of Pediatrics, Amiens-Picardie University Medical Center, Amiens, France.
J Pediatr Gastroenterol Nutr. 2025 Jan;80(1):113-123. doi: 10.1002/jpn3.12384. Epub 2024 Oct 16.
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.
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).
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.
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.
维多珠单抗和乌司奴单抗在诱导和维持成年炎症性肠病(IBD)患者无皮质类固醇临床缓解(CFR)方面有效。本研究描述了维多珠单抗和乌司奴单抗在儿童IBD中的疗效和安全性。
对法国北部三个中心接受维多珠单抗或乌司奴单抗治疗的所有18岁及以下克罗恩病(CD)或溃疡性结肠炎(UC)患者进行回顾性随访。主要结局是第14周(W14)时的CFR。
2016年至2021年期间,分别有25例患者(9例CD,16例UC)和33例患者(28例CD,5例UC)开始使用维多珠单抗和乌司奴单抗治疗。所有患者此前均接受过抗肿瘤坏死因子(TNF)治疗。维多珠单抗和乌司奴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。在接受维多珠单抗治疗的患者中,W14时36%达到CFR,其中CD患者为22%,UC患者为44%。在W52时,56%达到CFR,其中CD患者为33%,UC患者为69%。在接受乌司奴单抗治疗的患者中,W14时49%达到CFR,其中CD患者为54%,UC患者为20%。在W52时,55%达到CFR,其中CD患者为57%,UC患者为40%。维多珠单抗治疗的患者在W0至W52期间中位生长速度显著增加,增加了+2标准差(p = 0.0002)。维多珠单抗治疗期间报告了4例不良事件,乌司奴单抗治疗的患者未报告不良事件。
维多珠单抗和乌司奴单抗在诱导和维持儿童期IBD的CFR方面似乎有效。需要进行随机对照试验来证实这些结果。