Real‐world effectiveness and safety of ustekinumab for the treatment of Crohn's disease: the Scottish ustekinumab cohort
Autor: | Cher Shiong Chuah, Ian D. Arnott, Nikolas Plevris, Gareth R. Jones, Wai Liam Lam, Rebecca Hall, Amy Tyler, S Siakavellas, Jayne Saunders, Philip Jenkinson, Claire Kane, Jennifer Veryan, Andrew Robertson, Graham Naismith, Gillian H Bain, Iona Campbell, L Potts, Christopher Kelly, Daniel R. Gaya, Craig Mowat, H. Jafferbhoy, James Fulforth, John Paul Seenan, Diarmid Ian Sutherland, Charlie W. Lees, David Watts, Jonathan Macdonald |
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Rok vydání: | 2021 |
Předmět: |
Adult
Male medicine.medical_specialty Disease State Medicine Cohort Studies 03 medical and health sciences 0302 clinical medicine Crohn Disease Interquartile range Internal medicine Ustekinumab Humans Medicine Adverse effect Survival analysis Retrospective Studies Inflammation Crohn's disease Hepatology business.industry Remission Induction Gastroenterology Retrospective cohort study Middle Aged medicine.disease Treatment Outcome Scotland 030220 oncology & carcinogenesis Cohort Female 030211 gastroenterology & hepatology business medicine.drug |
Zdroj: | Journal of Gastroenterology and Hepatology. 36:2067-2075 |
ISSN: | 1440-1746 0815-9319 |
DOI: | 10.1111/jgh.15390 |
Popis: | BACKGROUND AND AIM Ustekinumab is a monoclonal antibody that targets interleukin-12/23. In Scotland, it was approved for the treatment of moderate to severe Crohn's disease in 2017. The objective of this study was to establish the real-world effectiveness and safety of ustekinumab in the treatment of Crohn's disease. METHODS We conducted a retrospective study of patients receiving ustekinumab across eight Scottish National Health Service health boards between 2017 and 2019. Inclusion criteria included a diagnosis of Crohn's disease with symptoms attributed to active disease plus objective signs of inflammation at baseline (C-reactive protein ≥ 5 mg/L or fecal calprotectin ≥ 250 μg/g or inflammation on endoscopy/magnetic resonance imaging) and completion of induction plus at least one clinical follow-up at 8 weeks. Kaplan-Meier survival analysis was used to establish 12-month cumulative rates of clinical remission, mucosal healing, deep remission, and perianal fistula response. Rates of serious adverse events were described quantitatively. RESULTS Our cohort consisted of 216 patients (female sex, 37.9%; median age, 39.0 years, interquartile range [IQR] 28.8-51.8 years; disease duration, 9.9 years, IQR 6.0-16.5 years; prior biologic, 98.6%) with a median follow-up of 35.0 weeks (IQR 17.4-52.0 weeks). Twelve-month cumulative rates of clinical remission, mucosal healing, and deep remission (clinical remission plus mucosal healing) were 32.0%, 32.7%, and 19.3%, respectively. In patients with active perianal disease (n = 37), the 12-month cumulative perianal response rate was 53.1%. The serious adverse event rate was 13.6 per 100 patient-years of follow-up. CONCLUSION Ustekinumab is a safe and effective treatment for the treatment of complex Crohn's disease. |
Databáze: | OpenAIRE |
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