Cargando…

Effectiveness and Safety of Tofacitinib in the Management of Ulcerative Colitis: A Brazilian Observational Multicentric Study

BACKGROUND: Ulcerative colitis (UC) is a chronic inflammatory bowel disease which affects the colorectal mucosa with a relapsing–remitting pattern. The therapeutic options currently available for the medical management of UC include many options. Tofacitinib is an oral small molecule, Janus kinase (...

Descripción completa

Detalles Bibliográficos
Autores principales: Perin, Ramir Luan, Magro, Daniela Oliveira, Andrade, Adriana Ribas, Argollo, Marjorie, Carvalho, Nayara Salgado, Damião, Adérson Omar Moura Cintra, Dotti, Adriana Zanoni, Ferreira, Sandro da Costa, Flores, Cristina, Ludvig, Juliano Coelho, Nones, Rodrigo Bremer, Queiroz, Natalia Sousa Freitas, Parra, Rogério Serafim, Steinwurz, Flavio, Teixeira, Fabio Vieira, Kotze, Paulo Gustavo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9855307/
https://www.ncbi.nlm.nih.gov/pubmed/36777366
http://dx.doi.org/10.1093/crocol/otac050
Descripción
Sumario:BACKGROUND: Ulcerative colitis (UC) is a chronic inflammatory bowel disease which affects the colorectal mucosa with a relapsing–remitting pattern. The therapeutic options currently available for the medical management of UC include many options. Tofacitinib is an oral small molecule, Janus kinase (JAK) inhibitor, more selective for JAK1 and JAK3, which reduces the inflammatory process involved in the pathogenesis of UC. METHODS: Retrospective observational multicentric study of patients with UC who used tofacitinib in any phase of their treatment. Clinical remission and response (according to Mayo score), mucosal healing, primary and secondary loss of response, discontinuation of the drug with possible causes, and the need for dose optimization or switching to biologicals, need for surgery and adverse events were evaluated. RESULTS: From a total of 56 included patients, clinical remission was observed in 43.6% at week 12, 54.5% at week 26, 57.9% at week 52, and 40% at the last follow-up visit. Clinical response was observed in 71.4%, 81.8%, 89.5%, and 61.8% at the same time periods, respectively. Mucosal healing rates were 50% and 17.8% needed colectomy. CONCLUSIONS: Tofacitinib was effective in induction and maintenance of clinical response and remission rates, compatible to other international real-word studies and meta-analyses.