Efficacy and Safety of Ustekinumab for Ulcerative Colitis Through 4 Years: Final Results of the UNIFI Long-Term Maintenance Study

Author:

Afif Waqqas1,Arasaradnam Ramesh P.2ORCID,Abreu Maria T.3,Danese Silvio4,Sandborn William J.5,Miao Ye6ORCID,Zhang Hongyan6,Panaccione Remo7,Hisamatsu Tadakazu8ORCID,Scherl Ellen J.9,Leong Rupert W.10ORCID,Rowbotham David S.11ORCID,Peyrin-Biroulet Laurent12,Sands Bruce E.13ORCID,Marano Colleen6ORCID

Affiliation:

1. Division of Gastroenterology, McGill University Health Centre, Montréal, Québec, Canada;

2. Warwick Medical School, University of Warwick & University Hospital Coventry, Coventry Warwickshire, UK;

3. University of Miami Miller School of Medicine, Miami, Florida, USA;

4. Gastroenterology and Endoscopy, IRCCS Ospedale San Raffaele and University Vita-Salute San Raffaele, Milano, Italy;

5. Division of Gastroenterology, University of California San Diego, La Jolla, California, USA;

6. Janssen Research & Development, LLC, Spring House, Pennsylvania, USA;

7. University of Calgary, Calgary, Alberta, Canada;

8. Department of Gastroenterology and Hepatology, Kyorin University School of Medicine, Tokyo, Japan;

9. Weill Cornell Medicine, New York Presbyterian Hospital, New York, New York, USA;

10. Concord Hospital and Macquarie University Hospital, Sydney, New South Wales, Australia;

11. Auckland City Hospital, Auckland, New Zealand;

12. Gastroenterology Department and Inserm U954, Nancy University Hospital, Vandœuvre-lès-Nancy, France;

13. Dr. Henry D. Janowitz Division of Gastroenterology, Icahn School of Medicine at Mount Sinai, New York, New York, USA.

Abstract

INTRODUCTION: Ulcerative colitis (UC) is a chronic condition that may require long-term treatment. We report the final efficacy and safety results of the UNIFI long-term extension study of ustekinumab in patients with UC through 4 years. METHODS: Ustekinumab induction responders who completed 44 weeks of maintenance treatment and agreed to enter the long-term extension continued their subcutaneous maintenance therapy (90 mg ustekinumab every 8 or 12 weeks [q8w or q12w] or placebo). Starting at week 56, randomized patients could receive dose adjustment to 90 mg q8w. Symptoms and adverse events were assessed through the study; endoscopic assessment was conducted at week 200. RESULTS: Of the 348 patients randomized to subcutaneous ustekinumab at maintenance baseline (q8w and q12w combined), 55.2% were in symptomatic remission at week 200. A greater proportion of biologic-naive patients (67.2% [117/174]) were in symptomatic remission than those with a history of biologic failure (41.6% [67/161]). Among patients in symptomatic remission at week 200, 96.4% were corticosteroid-free. Of the 171 patients with endoscopic evaluation at week 200, 81.6% (71/87) in the q12w group and 79.8% (67/84) in the q8w group had endoscopic improvement. From weeks 156 to the final safety visit (up to week 220), no deaths, major adverse cardiovascular events, or tuberculosis occurred in patients receiving ustekinumab. Nasopharyngitis, UC worsening, and upper respiratory tract infections were the most frequently reported adverse events. DISCUSSION: The long-term efficacy of ustekinumab maintenance in patients with UC was confirmed through 4 years. No new safety signals were observed. ClinicalTrials.gov number NCT02407236.

Funder

Janssen Research and Development

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Gastroenterology,Hepatology

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