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

被引:6
作者
Afif, Waqqas [1 ]
Arasaradnam, Ramesh P. [2 ,3 ]
Abreu, Maria T. [4 ]
Danese, Silvio [5 ,6 ]
Sandborn, William J. [7 ]
Miao, Ye [8 ]
Zhang, Hongyan [8 ]
Panaccione, Remo [9 ]
Hisamatsu, Tadakazu [10 ]
Scherl, Ellen J. [11 ]
Leong, Rupert W. [12 ,13 ]
Rowbotham, David S. [14 ]
Peyrin-Biroulet, Laurent [15 ,16 ]
Sands, Bruce E. [17 ]
Marano, Colleen [8 ]
机构
[1] McGill Univ Hlth Ctr, Div Gastroenterol, Montreal, PQ, Canada
[2] Univ Warwick, Warwick Med Sch, Coventry, Warwickshire, England
[3] Univ Hosp Coventry, Coventry, Warwickshire, England
[4] Univ Miami, Miller Sch Med, Miami, FL USA
[5] IRCCS Osped San Raffaele, Gastroenterol & Endoscopy, Milan, Italy
[6] Univ Vita Salute San Raffaele, Milan, Italy
[7] Univ Calif San Diego, Div Gastroenterol, La Jolla, CA USA
[8] Janssen Res & Dev LLC, Spring House, PA USA
[9] Univ Calgary, Calgary, AB, Canada
[10] Kyorin Univ, Sch Med, Dept Gastroenterol & Hepatol, Tokyo, Japan
[11] New York Presbyterian Hosp, Weill Cornell Med, New York, NY USA
[12] Concord Hosp, Sydney, NSW, Australia
[13] Macquarie Univ Hosp, Sydney, NSW, Australia
[14] Auckland City Hosp, Auckland, New Zealand
[15] Nancy Univ Hosp, Gastroenterol Dept, Vandoeuvre Les Nancy, France
[16] Nancy Univ Hosp, Inserm U954, Vandoeuvre Les Nancy, France
[17] Icahn Sch Med Mt Sinai, Dr Henry D Janowitz Div Gastroenterol, New York, NY USA
关键词
endoscopic improvement; long-term extension; symptomatic remission; ulcerative colitis; ustekinumab; INFLAMMATORY-BOWEL-DISEASE; THERAPY;
D O I
10.14309/ajg.0000000000002621
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
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.
引用
收藏
页码:910 / 921
页数:12
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