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dc.contributor.authorAllocca, Mariangela
dc.contributor.authorCatalano, Gaia
dc.contributor.authorSavarino, Edoardo V.
dc.contributor.authorChaparro, María
dc.contributor.authorLevartovsky, Asaf
dc.contributor.authorMichalopoulos, George
dc.contributor.authorViazis, Nikos
dc.contributor.authorFousekis, Fotis S.
dc.contributor.authorPsistakis, Andreas
dc.contributor.authorNoviello, Daniele
dc.contributor.authorNeto do Nascimento, Catarina
dc.contributor.authorCaron, Benedicte
dc.contributor.authorKitsou, Vassiliki
dc.contributor.authorBamias, Giogos
dc.contributor.authorGarcia Zarrabeitia, Maria Jose
dc.contributor.authorZacharopoulou, Eirini
dc.contributor.authorFoteinogiannopoulou, Kalliopi
dc.contributor.authorD'Amico, Ferdinando
dc.contributor.authorKoutroubakis, Ioannis
dc.contributor.authorEllul, Pierre
dc.contributor.otherUniversidad de Cantabriaes_ES
dc.date.accessioned2024-05-15T13:34:05Z
dc.date.available2024-05-15T13:34:05Z
dc.date.issued2023
dc.identifier.issn2050-6406
dc.identifier.issn2050-6414
dc.identifier.urihttps://hdl.handle.net/10902/32843
dc.description.abstractBackground: Ustekinumab and tofacitinib have recently been approved for the management of moderate to severe ulcerative colitis (UC). However, there is no evidence on how they should be positioned in the therapeutic algorithm. The aim of this study was to compare tofacitinib and ustekinumab as third-line therapies in UC patients in whom anti-TNF and vedolizumab had failed. Methods: This was a multicenter retrospective observational study. The primary outcome was disease progression, defined as the need for steroids, therapy escalation, UC-related hospitalization and/or surgery. Secondary outcomes were clinical remission, normalization of C-reactive protein, endoscopic remission, treatment withdrawal, and adverse events. Results: One-hundred seventeen UC patients were included in the study and followed for a median time of 11.6 months (q₁–q₃, 5.5-18.7). Overall, 65% of patients were treated with tofacitinib and 35% with ustekinumab. In the entire study cohort, 63 patients (54%) had disease progression during the follow-up period. Treatment with ustekinumab predicted increased risk of disease progression compared to treatment with tofacitinib in Cox regression analysis (HR: 1.93 [95% CI: 1.06-3.50] p = 0.030). Twenty-eight (68%) patients in the ustekinumab group and 35 (46%) in the tofacitinib group had disease progression over the follow-up period (log-rank test, p < 0.054). No significant differences were observed for the secondary outcomes. Six and 22 adverse events occurred in the ustekinumab and tofacitinib groups, respectively (15% vs. 31%, p = 0.11). Conclusions: Tofacitinib was more efficacious in reducing disease progression than ustekinumab in this cohort of refractory UC patients. However, prospective head-to-head clinical trials are needed as to confirm these data.es_ES
dc.description.sponsorshipACKNOWLEDGMENTS: The authors received no financial support for the research, authorship, and/or publication of this article. Open access funding provided by BIBLIOSAN.es_ES
dc.format.extent9 p.es_ES
dc.language.isoenges_ES
dc.publisherWiley-Blackwelles_ES
dc.rights© 2023 The Authors. United European Gastroenterology Journal published by Wiley Periodicals LLC. on behalf of United European Gastroenterology. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.es_ES
dc.sourceUnited European Gastroenterology Journal, 2023, 1-9es_ES
dc.subject.otherBiologicses_ES
dc.subject.otherInflammatory bowel diseasees_ES
dc.subject.otherTofacitinibes_ES
dc.titleComparison between tofacitinib and ustekinumab as a third-line therapy in refractory ulcerative colitis: multicenter international studyes_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publisherVersionhttps://doi.org/10.1002/ueg2.12492es_ES
dc.rights.accessRightsopenAccesses_ES
dc.identifier.DOI10.1002/ueg2.12492
dc.type.versionpublishedVersiones_ES


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