Ustekinumab for Crohn's Disease: Results of the ICC Registry, a Nationwide Prospective Observational Cohort Study

被引:160
作者
Biemans, Vince B. C. [1 ,2 ]
van der Meulen-de Jong, Andrea E. [3 ]
van der Woude, Christine J. [4 ]
Lowenberg, Mark [5 ]
Dijkstra, Gerard [6 ]
Oldenburg, Bas [7 ]
de Boer, Nanne K. H. [8 ,9 ]
van der Marel, Sander [10 ]
Bodelier, Alexander G. L. [11 ]
Jansen, Jeroen M. [12 ]
Haans, Jeoffrey J. L. [2 ]
Theeuwen, Rosaline [3 ]
de Jong, Dirk [1 ]
Pierik, Marie J. [2 ]
Hoentjen, Frank [1 ]
机构
[1] Radboud Univ Nijmegen, Dept Gastroenterol & Hepatol, Med Ctr, POB 9101,Code 455, NL-6500 HB Nijmegen, Netherlands
[2] Maastricht Univ, Dept Gastroenterol & Hepatol, Med Ctr, Maastricht, Netherlands
[3] Leiden Univ, Dept Gastroenterol & Hepatol, Med Ctr, Leiden, Netherlands
[4] Erasmus MC, Dept Gastroenterol & Hepatol, Rotterdam, Netherlands
[5] Univ Amsterdam, Acad Med Ctr, Dept Gastroenterol & Hepatol, Med Ctr, Amsterdam, Netherlands
[6] Univ Med Ctr Groningen, Dept Gastroenterol & Hepatol, Groningen, Netherlands
[7] Univ Med Ctr Utrecht, Dept Gastroenterol & Hepatol, Utrecht, Netherlands
[8] Vrije Univ Amsterdam, Amsterdam Univ, Med Ctr, Dept Gastroenterol & Hepatol, Amsterdam, Netherlands
[9] Gastroenterol & Metab Res Inst, Amsterdam, Netherlands
[10] Haaglanden Med Ctr, Dept Gastroenterol & Hepatol, The Hague, Netherlands
[11] Amphia Hosp, Dept Gastroenterol & Hepatol, Breda, Netherlands
[12] Onze Lieve Vrouw Hosp, Dept Gastroenterol & Hepatol, Amsterdam, Netherlands
关键词
Ustekinumab; Crohn's disease; ICC Registry; INFLAMMATORY-BOWEL-DISEASE; REAL-WORLD EXPERIENCE; MAINTENANCE THERAPY; ANTI-TNF; SUBCUTANEOUS USTEKINUMAB; INDUCTION; EFFICACY; OUTCOMES;
D O I
10.1093/ecco-jcc/jjz119
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background and Aims: Ustekinumab is approved for the treatment of Crohn's disease [CD]. Systematically registered prospective real-world data are scarce. We therefore aimed to study the effectiveness, safety and usage of ustekinumab for CD in everyday practice. Methods: We prospectively enrolled CD patients initiating ustekinumab in regular care between December 2016 and January 2019. Clinical (Harvey Bradshaw Index [HBI]), biochemical (C-reactive protein [CRP] and faecal calprotectin [FCP]), extra-intestinal manifestations and, peri-anal fistula activity, ustekinumab dosage, concomitant medication use, and adverse events were documented at weeks 0, 12, 24, and 52.The primary outcome was corticosteroid-free clinical remission. Results: In total, 221 CD patients were included (98.6% anti-tumour necrosis factor [TNF] and 46.6% vedolizumab exposed) with a median follow-up of 52.0 weeks [interquartile range 49.3-58.4]. Corticosteroid-free clinical remission rates at weeks 24 and 52 were 38.2% and 37.1%, respectively. An initial dosing schedule of 8 weeks, compared to 12 weeks, correlated with a lower discontinuation rate [20.0% vs 42.6%, p = 0.01], but comparable corticosteroid-free clinical remission at week 52 (46.3% [q8w] vs 34.6% [q12w], p = 0.20). There was no clinical benefit of combination therapy after 52 weeks when compared to ustekinumab monotherapy [combi 40.6% vs mono 36.0%, p = 0.64]. At baseline, 28 patients had active peri-anal fistula, of whom 35.7% showed complete clinical resolution after 24 weeks. During follow-up we encountered six severe infections [3.5 per 100 patient-years], with all patients being on concomitant immunosuppressant therapies. Ustekinumab treatment discontinuation was observed in 75 [33.9%] patients mainly due to lack of response. Conclusion: Ustekinumab is a relatively safe and effective treatment option for CD patients with prior failure of anti-TNF and anti-integrin therapies.
引用
收藏
页码:33 / 45
页数:13
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