Impact of Baseline Corticosteroid Use on the Efficacy and Safety of Upadacitinib in Patients with Ulcerative Colitis: A Post Hoc Analysis of the Phase 3 Clinical Trial Programme

Author:

Raine Tim1ORCID,Ishiguro Yoh2,Rubin David T3ORCID,Finney-Hayward Tricia4,Vladea Ramona5,Liu John6,Phillips Charles6,Cheng Erica7,Targownik Laura8ORCID,Loftus Edward V9ORCID

Affiliation:

1. Department of Gastroenterology, Addenbrooke’s Hospital, Cambridge University Hospitals , Cambridge , UK

2. Department of Clinical Research, Hirosaki General Medical Centre, National Hospital Organisation , Hirosaki , Japan

3. Medicine Inflammatory Bowel Disease Center, University of Chicago , Chicago, IL , USA

4. Former employee of AbbVie, Global Medical Affairs , Maidenhead , UK

5. AbbVie, Global Medical Affairs , North Chicago, IL , USA

6. AbbVie, Research and Development , North Chicago, IL , USA

7. AbbVie, Data and Statistical Sciences , North Chicago, IL , USA

8. Division of Gastroenterology and Hepatology, Mount Sinai Hospital, University of Toronto , Toronto, ON , Canada

9. Division of Gastroenterology and Hepatology, Mayo Clinic College of Medicine and Science , Rochester, MN , USA

Abstract

Abstract Background and Aims This post hoc analysis assessed the efficacy and safety of upadacitinib in patients with moderately to severely active ulcerative colitis stratified by corticosteroid use from the ulcerative colitis Phase 3 clinical trial programme. Methods Patients were randomised [1:2] to 8 weeks’ placebo or upadacitinib 45 mg once daily; Week 8 responders were re-randomised [1:1:1] to 52 weeks’ placebo or upadacitinib 15 or 30 mg daily. Corticosteroid dose was kept stable during induction but tapered according to a protocol-defined schedule [or investigator discretion] during maintenance Weeks 0–8. Efficacy outcomes and exposure-adjusted, treatment-emergent adverse event [TEAE] rates were assessed for induction and maintenance stratified by corticosteroid use at induction baseline. Results Overall, 377/988 [38%] patients were receiving corticosteroids at induction baseline [placebo, n = 133; upadacitinib 45 mg, n = 244] and 252 [37%] of the 681 clinical responders who entered maintenance were on corticosteroids at induction baseline [n = 84 for each treatment]. Similar proportions of patients receiving upadacitinib achieved clinical remission per Adapted Mayo Score with and without baseline corticosteroids at Weeks 8 and 52. The total proportion of patients re-initiating corticosteroids was higher with placebo [24/84;29%] vs upadacitinib 15 mg [16/81; 20%)] and 30 mg [11/81; 14%]. During induction, patients receiving corticosteroids at baseline had higher rates of TEAEs, serious TEAEs, and serious infections vs those not receiving corticosteroids; however, TEAE rates were similar during maintenance after corticosteroid withdrawal. Conclusions Upadacitinib is an effective steroid-sparing treatment in patients with moderately to severely active ulcerative colitis. Clinicaltrials.gov identifiers: NCT02819635; NCT03653026

Funder

AbbVie

Publisher

Oxford University Press (OUP)

Subject

Gastroenterology,General Medicine

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