2017
DOI: 10.1093/ecco-jcc/jjx082
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Vedolizumab in Paediatric Inflammatory Bowel Disease: A Retrospective Multi-Centre Experience From the Paediatric IBD Porto Group of ESPGHAN

Abstract: Vedolizumab was safe and effective in this cohort of paediatric refractory IBD. These data support previous findings of slow induction rate of vedolizumab in CD and a trend to be less effective compared with patients with UC.

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Cited by 82 publications
(84 citation statements)
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References 22 publications
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“…176 The retrospective case reports of pediatric patients with IBD found that vedolizumab tended to be slower acting and have lower remission rates in patients with CD compared to those with ulcerative colitis. 177,178 Long-term, open-label follow-up data report low rates of infusion reactions, serious infections, and malignancy. 179,180 The consensus group did not make a recommendation for or against the use of vedolizumab in patients who had failed prior anti-TNF therapy.…”
Section: No Consensus Mmentioning
confidence: 99%
“…176 The retrospective case reports of pediatric patients with IBD found that vedolizumab tended to be slower acting and have lower remission rates in patients with CD compared to those with ulcerative colitis. 177,178 Long-term, open-label follow-up data report low rates of infusion reactions, serious infections, and malignancy. 179,180 The consensus group did not make a recommendation for or against the use of vedolizumab in patients who had failed prior anti-TNF therapy.…”
Section: No Consensus Mmentioning
confidence: 99%
“…Ledder et al. on behalf of the ESPGHAN Porto group report 41 children; 33 had UC,and 8 had IBD‐Unclassified . Median PUCAI for these 41 children was 45 at start of treatment, and all had received anti‐TNF.…”
Section: Characteristics and Response Of Children To Vedolizumab For mentioning
confidence: 99%
“…ESPGHAN recently published the largest multicenter case series of 64 children, mean 14.5 (range 2–18) years old and treated with vedolizumab. No serious drug‐related AEs were reported at a median follow up of 24 weeks (IQR 14–38, range 6–116) …”
Section: Vedolizumabmentioning
confidence: 99%
“…No serious drugrelated AEs were reported at a median follow up of 24 weeks (IQR 14-38, range 6-116). 30 Elderly. Post hoc analysis of the GEMINI 1 and 2 trials was performed, with patients stratified by age into <35, 35-54, and > 55 years old.…”
Section: Safety Of Vedolizumab In Special Populationsmentioning
confidence: 99%