Efficacy and Safety of Maintenance Ustekinumab for Ulcerative Colitis Through 3 Years: UNIFI Long-term Extension

Author:

Abreu Maria T1,Rowbotham David S2,Danese Silvio3,Sandborn William J4,Miao Ye5,Zhang Hongyan5,Tikhonov Ilia5,Panaccione Remo6,Hisamatsu Tadakazu7,Scherl Ellen J8,Leong Rupert W9,Arasaradnam Ramesh P10,Afif Waqqas11,Peyrin-Biroulet Laurent12,Sands Bruce E13,Marano Colleen5

Affiliation:

1. Division of Gastroenterology, Department of Medicine, University of Miami Miller School of Medicine , Miami, FL , USA

2. Department of Gastroenterology & Hepatology, Auckland City Hospital , Auckland , New Zealand

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

4. Division of Gastroenterology, University of California San Diego , La Jolla, CA, USA

5. Janssen Research & Development LLC., Immunology , Spring House, PA , USA

6. Inflammatory Bowel Disease Unit, Division of Gastroenterology and Hepatology, University of Calgary , Calgary, AB , Canada

7. Department of Internal Medicine, Kyorin University School of Medicine , Tokyo , Japan

8. Jill Roberts Center for Inflammatory Bowel Disease, New York Presbyterian Weill Cornell Medical College , New York, NY , USA

9. Gastroenterology and Liver Services Concord Hospital and Department of Gastroenterology Macquarie University Hospital , Sydney, NSW , Australia

10. Department of Gastroenterology, University Hospital Coventry & Warwickshire NHS Trust , Coventry , UK

11. Division of Gastroenterology, McGill University Health Centre , Montreal, QC , Canada

12. University of Lorraine, CHRU-Nancy, Department of Gastroenterology and Nutrition, Genetics, and Environmental Risk Exposure , Nancy , France

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

Abstract

Abstract Background and Aims The UNIFI long-term extension [LTE] study reports the efficacy and safety of subcutaneous 90 mg ustekinumab through 3 years of maintenance therapy. Methods Patients randomised to ustekinumab every 12 weeks [q12w] or every 8 weeks [q8w] at maintenance baseline [N = 348] and randomised ustekinumab-treated patients in the LTE [N = 284] were evaluated. Symptomatic remission [Mayo stool frequency = 0/1, rectal bleeding = 0] was assessed. Safety included all LTE patients [N = 188 placebo and N = 457 ustekinumab]. Results Among patients randomised to the ustekinumab q12w and q8w groups at maintenance baseline, 54.1% and 56.3% achieved symptomatic remission at Week 152, respectively. Overall, 20% of patients discontinued ustekinumab, 10% of biologic-naïve and 30% of biologic-exposed patients. Among patients in symptomatic remission at Year 3, 94.6% and 98.0% of patients were also corticosteroid free, respectively. Corticosteroid-free symptomatic remission rates in the ustekinumab q12w and q8w groups were 51.2% and 55.1% at Week 152, respectively. Remission rates were higher for biologic-naïve patients than for those with a history of biologic failure. Biochemical evidence of response was demonstrated by stable, decreased C-reactive protein and faecal calprotectin measurements over 3 years. From Weeks 96 to 156, no deaths, major adverse cardiovascular events, or tuberculosis occurred. Nasopharyngitis, ulcerative colitis, and upper respiratory tract infection were most frequently reported. One ustekinumab-treated patient with a history of basal cell carcinoma [BCC] reported two BCCs. One patient in the q8w ustekinumab group, who was receiving concomitant 6-mercaptopurine, experienced serious adverse events of neutropenic sepsis and oral herpes. Conclusions Efficacy of ustekinumab in patients with ulcerative colitis was confirmed through 3 years. No new safety signals were observed.

Funder

Janssen Research & Development, LLC

Publisher

Oxford University Press (OUP)

Subject

Gastroenterology,General Medicine

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