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One‐year outcomes with ustekinumab therapy in infliximab‐refractory paediatric ulcerative colitis: a multicentre prospective study
Author(s) -
Dhaliwal Jasbir,
McKay Hayley E.,
Deslandres Colette,
Debruyn Jennifer,
Wine Eytan,
Wu Ashley,
Huynh Hien,
Carman Nicholas,
Crowley Eileen,
Church Peter C.,
Walters Thomas D.,
Ricciuto Amanda,
Griffiths Anne M.
Publication year - 2021
Publication title -
alimentary pharmacology and therapeutics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.308
H-Index - 177
eISSN - 1365-2036
pISSN - 0269-2813
DOI - 10.1111/apt.16388
Subject(s) - medicine , ustekinumab , vedolizumab , ulcerative colitis , infliximab , clinical endpoint , faecal calprotectin , refractory (planetary science) , gastroenterology , intention to treat analysis , surgery , calprotectin , inflammatory bowel disease , clinical trial , tumor necrosis factor alpha , disease , physics , astrobiology
Summary Background The phase 3 (UNIFI) trial of ustekinumab (anti‐interleukin 12/23) demonstrated efficacy even after prior biologic failure in adult ulcerative colitis (UC), but paediatric data are lacking. Aim To prospectively monitor efficacy and serum concentrations of ustekinumab given to children with UC refractory to other biologics. Methods Children with anti‐TNF refractory UC initiating ustekinumab intravenously at sites of the Canadian Children IBD Network prior to 12/2019 are included. The primary endpoint was steroid‐free clinical remission with subcutaneous ustekinumab at 52 weeks (Paediatric Ulcerative Colitis Activity Index <10, no steroids ≥4 weeks). Ustekinumab levels were measured after week 20. Endoscopic improvement was defined as Mayo endoscopic subscore ≤1, or faecal calprotectin (FCP) <250 μg/g if not re‐colonoscoped. Results At six sites between 01/2018 and 11/2019, 25 children (median [IQR] age 14.8 years [12.3‐16.2], 72% female) with UC duration 2.3 years (1.1‐4.2) received intravenous ustekinumab (median dose/kg of 6.4 [5.5‐7.5] mg). All patients had failed prior infliximab therapy, and 12 (48%) also vedolizumab. Five patients discontinued ustekinumab after IV induction (four undergoing colectomy). On intent to treat basis, 44% achieved the primary endpoint of steroid‐free remission at week 52, including nine (69%) of 13 who previously treated with anti‐TNF only vs two (17%) of 12 who previously failed also by vedolizumab ( P = 0.008). Seven of 11 remitters met the criteria for endoscopic improvement. The median (IQR) trough levels (μg/mL) were greater with q4 vs q8 weekly dosing (8.7 [4.6‐9.9] vs 3.8 [12.7‐4.8]) P = 0.02, but greater exposure was not associated with a superior rate of clinical remission. No adverse events were associated with therapy. Conclusion Ustekinumab demonstrated efficacy in this paediatric cohort with otherwise treatment‐refractory UC. Treatment failure was not due to inadequate drug exposure.