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dc.contributorHospital General de Granollers
dc.contributor.authorGisbert, Javier Pérez
dc.contributor.authorDonday, María G
dc.contributor.authorRiestra Menéndez, Sabino
dc.contributor.authorBenitez, Jose Manuel
dc.contributor.authorNavarro-Llavat, Mercè
dc.contributor.authorBusquets, David
dc.contributor.authorSerra Nilsson, Katja
dc.contributor.authorLucendo, Alfredo J
dc.contributor.authorMorales Alvarado, Víctor Jair
dc.date.accessioned2025-05-12T10:15:28Z
dc.date.available2025-05-12T10:15:28Z
dc.date.issued2025-02-06
dc.identifier.citationGisbert JP, Donday MG, Riestra S, Lucendo AJ, Benítez JM, Navarro-Llavat, et al. Withdrawal of antitumour necrosis factor in inflammatory bowel disease patients in remission: a randomised placebo-controlled clinical trial of GETECCU. Gut. 2025 Feb 6;74(3):387-396.
dc.identifier.issn1468-3288
dc.identifier.urihttp://hdl.handle.net/11351/13073
dc.descriptionInflammatory bowel disease; Inflixmab; Ulcerative colitis
dc.description.abstractPrimary objectives: to compare the rates of sustained clinical remission at 12 months in patients treated with antitumour necrosis factor (anti-TNF) and immunomodulators who withdraw anti-TNF treatment versus those who maintain it. to evaluate the effect of anti-TNF withdrawal on relapse-free time, endoscopic and radiological activity, safety, quality of life and work productivity; and to identify predictive factors for relapse. Prospective, quadruple-blind, multicentre, randomised, controlled trial. Patients with ulcerative colitis or Crohn's disease in clinical remission for >6 months and absence of severe endoscopic (and radiological in Crohn's disease) lesions were randomised to maintain anti-TNF treatment (maintenance arm (MA)) or to withdraw it (withdrawal arm (WA)). All patients maintained immunomodulators. Patients were followed-up until month 12 or up to clinical relapse. One-hundred forty patients were randomised: 70 were allocated to the MA and 70 to the WA. The proportion of patients with sustained clinical remission at 12 months was similar in the MA and WA: 59/70 (84%), 95% CI=74% to 92% versus 53/70 (76%), 95% CI=64% to 85%. The proportion of patients with significant endoscopic lesions at the end of follow-up was 8.5% in the MA and 19% in the WA (p=0.1); a higher proportion of patients had faecal calprotectin >250 µg/g at the end of follow-up in the WA (p=0.01). The same percentage of patients in both groups had at least one adverse event (69%). The proportion of patients with serious adverse events was also similar in both groups (4% in MA vs 7% in WA). Anti-TNF withdrawal in selected patients with IBD in clinical, endoscopic and radiological remission has no impact on sustained clinical remission at 1 year although objective markers of activity were higher in patients who withdrew treatment. https://www.clinicaltrialsregister.eu/ctr-search/search?query=2015-001410-10 https://clinicaltrials.gov/study/NCT02994836.
dc.language.isoeng
dc.publisherBMJ Publishing Group
dc.relation.ispartofseriesGut;74(3)
dc.rightsAttribution-NonCommercial 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by-nc/4.0/
dc.sourceScientia
dc.subjectAparell digestiu - Malalties
dc.subjectColitis ulcerosa
dc.subjectMalalties - Recaiguda
dc.subject.meshInflammatory Bowel Diseases
dc.subject.meshColitis, Ulcerative
dc.subject.meshInfliximab
dc.titleWithdrawal of antitumour necrosis factor in inflammatory bowel disease patients in remission: a randomised placebo-controlled clinical trial of GETECCU
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1136/gutjnl-2024-333385
dc.subject.decsenfermedad inflamatoria intestinal
dc.subject.decscolitis ulcerosa
dc.subject.decsinfliximab
dc.relation.publishversionhttps://www.doi.org/10.1136/gutjnl-2024-333385
dc.type.versioninfo:eu-repo/semantics/publishedVersion
dc.audienceProfessionals
dc.contributor.authoraffiliation[Gisbert JP, Donday MG] Gastroenterology Department, Hospital Universitario de La Princesa, Instituto de Investigación Sanitaria Princesa (IIS- Princesa), Universidad Autónoma de Madrid (UAM), Madrid, Spain. Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBEREHD), Madrid, Spain. [Riestra S] Gastroenterology Department, Hospital Universitario Central de Asturias, e Instituto de Investigación Sanitaria del Principado de Asturias (ISPA), Oviedo, Spain. [Lucendo AJ] Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBEREHD), Madrid, Spain. Gastroenterology Department, Hospital General de Tomelloso, Instituto de Investigación Sanitaria de Castilla- La Mancha (IDISCAM), Tomelloso, Spain. [Benítez JM] Gastroenterology Department, Hospital Universitario Reina Sofía, IMIBIC, Cordoba, Spain. [Navarro-Llavat M] Servei de Digestologia, Hospital de Sant Joan Despí Moisès Broggi, Barcelona, Spain. [Morales-Alvarado VJ] Àrea d’aparell digestiu, Hospital General de Granollers, Granollers, Spain. [Busquets D] Servei de Digestiu, Hospital Dr. Josep Trueta, IDIBGI, Girona, Spain. [Serra Nilsson] Servei d'Aparell Digestiu, Hospital Universitari de Bellvitge, L'Hospitalet de Llobregat, Spain
dc.identifier.pmid39794921
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess


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