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Long-term effectiveness and safety of ustekinumab in bio-naïve and bio-experienced anti-tumor necrosis factor patients with Crohn’s disease: a real-world multicenter Brazilian study

Authors :
Rogério Serafim Parra
Júlio Maria Fonseca Chebli
Natália Sousa Freitas Queiroz
Aderson Omar Mourão Cintra Damião
Matheus Freitas Cardoso de Azevedo
Liliana Andrade Chebli
Erika Ruback Bertges
Antonio José Tiburcio Alves Junior
Orlando Ambrogini Junior
Bianca Loyo Pona Schiavetti da Silva
Marcio Lubini
Mauro Bafutto
Cristina Flores
Eduardo Garcia Vilela
Sandra Felice Boratto
Newton Luiz Tricarico Gasparetti Junior
Flavio Steinwurz
Nayara Salgado Carvalho
Omar Féres
José Joaquim Ribeiro da Rocha
Source :
BMC Gastroenterology, Vol 22, Iss 1, Pp 1-12 (2022)
Publication Year :
2022
Publisher :
BMC, 2022.

Abstract

Abstract Background The effectiveness of ustekinumab (UST) in the treatment of Crohn’s disease (CD) has been demonstrated in the pivotal Phase 3 UNITI 1 and 2 and IM-UNITI studies in both anti-TNF-naïve and anti-TNF-exposed patients. Given the selective nature of pivotal trial designs, real-world effectiveness and safety studies are warranted. We report our experience with UST treatment in a large, real-world multicenter cohort of Brazilian patients with CD. Methods We performed a retrospective multicenter study including patients with CD, predominantly biologically refractory CD, who received UST. The primary endpoint was the proportion of patients in clinical remission at weeks 8, 24 and 56. Possible predictors of clinical and biological response/remission and safety outcomes were also assessed. Results Overall, 245 CD (mean age 39.9 [15–87]) patients were enrolled. Most patients (86.5%) had been previously exposed to biologics. According to nonresponder imputation analysis, the proportions of patients in clinical remission at weeks 8, 24 and 56 were 41.0% (n = 98/239), 64.0% (n = 153/239) and 39.3% (n = 94/239), respectively. A biological response was achieved in 55.4% of patients at week 8, and 59.3% were in steroid-free remission at the end of follow-up. No significant differences in either clinical or biological remission were noted between bio-naïve and bio-experienced patients. Forty-eight patients (19.6%) presented 60 adverse events during the follow-up, of which 8 (13.3%) were considered serious adverse events (3.2% of 245 patients). Overall, a proximal disease location, younger age, perianal involvement, and smoking were associated with lower rates of clinical remission over time. Conclusions UST therapy was effective and safe in the long term in this large real-life cohort of Brazilian patients with refractory CD, regardless of previous exposure to other biological agents.

Details

Language :
English
ISSN :
1471230X
Volume :
22
Issue :
1
Database :
Directory of Open Access Journals
Journal :
BMC Gastroenterology
Publication Type :
Academic Journal
Accession number :
edsdoj.1ae676670dde47428b23d064b72c8265
Document Type :
article
Full Text :
https://doi.org/10.1186/s12876-022-02280-3