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

Author:

Perin Ramir Luan1ORCID,Magro Daniela Oliveira2ORCID,Andrade Adriana Ribas3ORCID,Argollo Marjorie4ORCID,Carvalho Nayara Salgado4ORCID,Damião Adérson Omar Moura Cintra5ORCID,Dotti Adriana Zanoni6ORCID,Ferreira Sandro da Costa7ORCID,Flores Cristina8ORCID,Ludvig Juliano Coelho9ORCID,Nones Rodrigo Bremer10ORCID,Queiroz Natalia Sousa Freitas11ORCID,Parra Rogério Serafim6ORCID,Steinwurz Flavio12ORCID,Teixeira Fabio Vieira13ORCID,Kotze Paulo Gustavo14ORCID

Affiliation:

1. Universidade de Passo Fundo (UPF) , Passo Fundo , Brazil

2. Universidade Estadual de Campinas (UNICAMP) , Campinas , Brazil

3. Universidade Estadual da Bahia (UNEB) , Salvador , Brazil

4. Hospital São Luiz (Rede D’or) , São Paulo , Brazil

5. Universidade de São Paulo (USP) , São Paulo , Brazil

6. Hospital de Clínicas das UFPR , Curitiba , Brazil

7. Faculdade de Medicina de Ribeirão Preto da Universidade de São Paulo (FMRPUSP) , Ribeirão Preto , Brazil

8. Instituto do Aparelho Digestivo (IAD) , Porto Alegre , Brazil

9. Clínica ESADI , Blumenau , Brazil

10. Hospital Nossa Senhora das Graças , Curitiba , Brazil

11. Hospital Santa Cruz , Curitiba , Brazil

12. Hospital Israelita Albert Einstein , São Paulo , Brazil

13. Clínica Gastrosaúde , Marília , Brazil

14. Pontificia Universidade Católica do Paraná (PUCPR) , Curitiba , Brazil

Abstract

Abstract 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.

Funder

WyethPfizer

Publisher

Oxford University Press (OUP)

Subject

Gastroenterology

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