Real-Life Efficacy of Tofacitinib in Various Situations in Ulcerative Colitis: A Retrospective Worldwide Multicenter Collaborative Study

TFB Study Group

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4 Citationer (Scopus)

Abstract

Background and Aims: Tofacitinib (TFB) appears to be effective in the treatment of ulcerative colitis (UC); however, available real-world studies are limited by cohort size. TFB could be an option in the treatment of acute severe ulcerative colitis (ASUC). We aimed to investigate efficacy and safety of TFB in moderate-to-severe colitis and ASUC. Methods: This retrospective, international cohort study enrolling UC patients with ≥6-week follow-up period was conducted from February 1 to July 31, 2022. Indications were categorized as ASUC and chronic activity (CA). Baseline demographic and clinical data were obtained. Steroid-free remission (SFR), colectomy, and safety data were analyzed. Results: A total of 391 UC patients (median age 38 [interquartile range, 28-47] years; follow-up period 26 [interquartile range, 14-52] weeks) were included. A total of 27.1% received TFB in ASUC. SFR rates were 23.7% (ASUC: 26.0%, CA: 22.8%) at week 12 and 41.1% (ASUC: 34.2%, CA: 43.5%) at week 52. The baseline partial Mayo score (odds ratio [OR], 0.850; P = .006) was negatively associated with week 12 SFR, while biologic-naïve patients (OR, 2.078; P = .04) more likely achieved week 52 SFR. The colectomy rate at week 52 was higher in ASUC group (17.6% vs 5.7%; P < .001) and decreased with age (OR, 0.94; P = .013). A total of 67 adverse events were reported, and 17.9% resulted in cessation of TFB. One case of thromboembolic event was reported. Conclusions: TFB is effective in both studied indications. TFB treatment resulted in high rates of SFR in the short and long terms. Higher baseline disease activity and previous biological therapies decreased efficacy. No new adverse event signals were found.

OriginalsprogEngelsk
TidsskriftInflammatory Bowel Diseases
Vol/bind30
Udgave nummer5
Sider (fra-til)768-779
Antal sider12
ISSN1078-0998
DOI
StatusUdgivet - 2024

Bibliografisk note

Funding Information:
This work was supported by the research grants of Hungarian Scientific Research Fund (K22-143549), the National Research, Development and Innovation Office (Grant IDs: 125377, 129266, and 134863), the New National Excellence Program of the Ministry of Human Capacities (UNKP-22-3-SZTE-278 to T.R., UNKP-22-5-SZTE-545 to R.B., UNKP-22-4 -SZTE-296 to A.F., UNKP-21-5-SZTE-552 to K.F., UNKP-22-3-SZTE-233 to P.B.), and Janos Bolyai Research Grant (BO/00598/19/5 to K.F. and BO/00723/22 to R.B.) and the G\u00E9za Het\u00E9nyi Research Grant (to K.F., M.R., and A.B.) by the Albert Szent-Gy\u00F6rgyi Medical School, University of Szeged.

Funding Information:
This work was supported by the research grants of Hungarian Scientific Research Fund (K22-143549), the National Research, Development and Innovation Office (Grant IDs: 125377, 129266, and 134863), the New National Excellence Program of the Ministry of Human Capacities (UNKP-22-3-SZTE-278 to T.R., UNKP-22-5-SZTE-545 to R.B., UNKP-22-4 -SZTE-296 to A.F., UNKP-21-5-SZTE-552 to K.F., UNKP-22-3-SZTE-233 to P.B.), and Janos Bolyai Research Grant (BO/00598/19/5 to K.F. and BO/00723/22 to R.B.) and the G\u00E9za Het\u00E9nyi Research Grant (to K.F., M.R., and A.B.) by the Albert Szent-Gy\u00F6rgyi Medical School, University of Szeged.s

Publisher Copyright:
© 2023 Crohn's & Colitis Foundation. Published by Oxford University Press on behalf of Crohn's & Colitis Foundation.

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