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Ustekinumab and vedolizumab for the prevention of postoperative recurrence of Crohn's disease: Results from the ENEIDA registry

Authors :
Míriam Mañosa
Agnès Fernández-Clotet
Pilar Nos
María Dolores Martín-Arranz
Noemí Manceñido
Ana Carbajo
Esther Hinojosa
Alejandro Hernández-Camba
Roser Muñoz-Pérez
Maia Boscá-Watts
Marta Calvo
Mónica Sierra-Ausín
Eugenia Sánchez-Rodríguez
Manuel Barreiro-de Acosta
Alejandro Núñez-Alonso
Yamile Zabana
Lucía Márquez
Javier P Gisbert
Jordi Guardiola
Empar Sáinz
Pedro Delgado-Guillena
David Busquets
Manuel van Domselaar
Eva Girona
Rufo Lorente
Diego Casas-Deza
José M. Huguet
Sergio Maestro
M. José Cabello
Jesús Castro
Marisa Iborra
Fiorella Cañete
Margalida Calafat
Eugeni Domènech
Source :
Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver, r-INCLIVA. Repositorio Institucional de Producción Científica de INCLIVA, instname, r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
Publication Year :
2022
Publisher :
ELSEVIER SCIENCE INC, 2022.

Abstract

BACKGROUND: Anti-TNF agents are the only effective biological agents for the prevention of postoperative recurrence (POR) in Crohn's disease (CD). However, they are contraindicated or have been shown to fail in some patients. Although ustekinumab and vedolizumab were licensed for CD some years ago, data in this setting are scarce.; METHODS: All CD patients in whom ustekinumab or vedolizumab was prescribed for the prevention of POR within three months of ileocolonic resection with anastomosis were identified from the ENEIDA registry. The development of endoscopic, clinical and surgical POR was registered.; RESULTS: Forty patients were treated for the prevention of POR with ustekinumab and 25 were treated with vedolizumab. Eighty per cent had at least one risk factor for POR (prior resections, active smoking, perianal disease or penetrating disease behaviour). All the patients had been exposed to anti-TNF therapy. After a median follow-up of 17 and 26 months, the cumulative probability of clinical POR at 12 months after surgery was 32% and 30% for ustekinumab and vedolizumab, respectively. Endoscopic assessment within the first 18 months after surgery was available for 80% of the patients on ustekinumab and 70% for those on vedolizumab. The rate of endoscopic POR was 42% for ustekinumab and 40% for vedolizumab. One patient treated with ustekinumab and two with vedolizumab underwent a new intestinal resection.; CONCLUSIONS: Ustekinumab and vedolizumab seem to be effective in the prevention of POR in patients at high risk. Our results warrant controlled trials comparing these drugs with conventional therapies. Copyright © 2022. Published by Elsevier Ltd.

Details

ISSN :
15908658
Database :
OpenAIRE
Journal :
Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver, r-INCLIVA. Repositorio Institucional de Producción Científica de INCLIVA, instname, r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
Accession number :
edsair.doi.dedup.....02e56f8311094437ffa36b32a9ac8100