Positioning Ustekinumab in Crohn's Disease: From Clinical Evidence to Clinical Practice

被引:14
|
作者
Danese, Silvio [1 ,2 ]
Bonovas, Stefanos [2 ]
Peyrin-Biroulet, Laurent [3 ,4 ]
机构
[1] Humanitas Univ, Dept Biomed Sci, Via Manzoni 113, I-20089 Milan, Italy
[2] Humanitas Clin & Res Ctr, Dept Gastroenterol, Milan, Italy
[3] Lorraine Univ, Univ Hosp Nancy, Dept Hepatogastroenterol, Vandoeuvre Les Nancy, France
[4] Lorraine Univ, INSERM, U954, Vandoeuvre Les Nancy, France
关键词
Ustekinumab; Crohn's disease; INFLAMMATORY-BOWEL-DISEASE; ANTI-IL-12/23P40; MONOCLONAL-ANTIBODY; LONG-TERM SAFETY; NETWORK METAANALYSIS; MAINTENANCE THERAPY; SUBCUTANEOUS USTEKINUMAB; ANKYLOSING-SPONDYLITIS; RHEUMATOID-ARTHRITIS; EXPERIMENTAL COLITIS; PSORIATIC-ARTHRITIS;
D O I
10.1093/ecco-jcc/jjx079
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Biological medicines have revolutionised the treatment of Crohn's disease [CD]. Yet, the management of patients not responding to tumour necrosis factor [TNF] antagonists remains a clinical challenge. Ustekinumab is a human monoclonal antibody blocking the biological activity of interleukins 12 and 23, which regulate the immune system and immune-mediated inflammatory disorders. Ustekinumab has recently been approved for the treatment of adult patients with moderately to severely active CD, who have had an inadequate response with, lost response to, or were intolerant to either conventional therapy or a TNF antagonist, or have medical contraindications to such therapies. Herein, we review the new biological drug's efficacy and safety data reported from randomised controlled trials and real-world observational studies conducted in populations with CD, in order to identify the patient groups most likely to benefit, and to appropriately place ustekinumab into treatment algorithms for CD.
引用
收藏
页码:1258 / 1266
页数:9
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