Sequencing JAK-inhibitors in ulcerative colitis effectiveness and safety of switching within treatment class /

Evidence from rheumatology supports a within-class treatment switch for JAK-inhibitors (JAKi), but data in ulcerative colitis (UC) remain limited. We aimed to assess the effectiveness and safety of initiating a second JAKi in patients with UC previously treated with another JAKi.We conducted a multi...

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Bibliográfiai részletek
Szerzők: Innocenti Tommaso
Hanžel Jurij
Truyens Marie
Lukaš Milan
Gordon Hannah
Cremer Anneline
Molnár Tamás
Julsgaard Mette
Onali Sara
Todeschini Alessia
Nardone Olga Maria
Noor Nurulamin M
Caprioli Flavio
Scaldaferri Franco
Argyriou Konstantinos
Savarino Edoardo Vincenzo
Brinar Marko
Hedin Charlotte R H
Vela González Milagros
Armuzzi Alessandro
Blesl Andreas
Aratari Annalisa
Quadarella Alessandro
Parigi Tommaso Lorenzo
Bertani Lorenzo
Ferracane Concetta
Uzzan Mathieu
Michalopoulos George
De Bernardi Alice
Katsanos Konstantinos
Farkas Bernadett
et al
Dokumentumtípus: Cikk
Megjelent: 2026
Sorozat:JOURNAL OF CROHNS & COLITIS 20 No. 2
Tárgyszavak:
doi:10.1093/ecco-jcc/jjaf188

mtmt:36424807
Online Access:http://publicatio.bibl.u-szeged.hu/39423
Leíró adatok
Tartalmi kivonat:Evidence from rheumatology supports a within-class treatment switch for JAK-inhibitors (JAKi), but data in ulcerative colitis (UC) remain limited. We aimed to assess the effectiveness and safety of initiating a second JAKi in patients with UC previously treated with another JAKi.We conducted a multicentre retrospective study, including patients with UC starting a second JAKi after prior JAKi exposure. The primary endpoint was week 12 steroid-free clinical remission (SFCR-rectal bleeding subscore = 0, stool frequency subscore ≤ 1, and no steroids).We included 243 patients [median follow-up: 38 (21-57) weeks]. At weeks 12, 26, and 52, SFCR was achieved in 116/243 (48%), 120/243 (49%), and 69/243 (28%), respectively. Secondary loss of response to the first JAKi was associated with higher SFCR at week 12 compared to primary failure (OR = 1.92, 95%CI = 1.11-3.30, p = 0.02). Higher baseline disease activity (OR = 0.68, 95%CI = 0.68-0.55, p < 0.01) and steroid use (OR = 0.23, 95%CI = 0.13-0.42, p < 0.01) had lower odds of week 12 SFCR. Endoscopic remission occurred in 22/243 (9%) (<week 26) and 27/243 (11%) (26-78 weeks), and endoscopic improvement in 53/243 (22%) and 45/243 (19%), respectively. Sixty-seven (28%) patients discontinued the second JAKi, mostly due to primary (36/67) or secondary failure (22/67). Sixty-six adverse events (mostly acne and infections) occurred in 56 (23%) patients, without major thromboembolic or cardiovascular events.Treatment with a second JAKi is effective and safe in patients with UC already exposed to JAKi. Primary failure to a first JAKi and steroid use at initiation of the second JAKi might reduce the likelihood of success with the second JAKi.
Terjedelem/Fizikai jellemzők:12
ISSN:1873-9946