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乌司奴单抗治疗克罗恩病的专家意见。

Ustekinumab in the management of Crohn's disease: Expert opinion.

机构信息

IBD Unit Presidio Columbus, Fondazione Policlinico Gemelli Università Cattolica, Rome, Italy.

UOC Gastroenterologia e Endoscopia Digestiva ASST Fatebenefratelli Sacco - DIBIC "L. Sacco" Università degli Studi, Milan, Italy.

出版信息

Dig Liver Dis. 2018 Jul;50(7):653-660. doi: 10.1016/j.dld.2018.02.017. Epub 2018 Mar 11.

Abstract

This expert-opinion paper reviews available evidence for the use of ustekinumab, a human interleukin 12/23 monoclonal antibody, in the treatment of Crohn's disease and discusses its potential role in the current treatment scenario for the condition. Ustekinumab appears to be associated with rapid and sustained clinical effect, as reported from the clinical research program, with additional support for potential mucosal healing. These characteristics are paralleled by a favorable safety profile, lack of immunogenicity and the presence of systemic anti-inflammatory activity. Importantly, ustekinumab requires only one single intravenous administration, while subsequent dosing is administered subcutaneously, with potential advantages for home-based therapy. Lastly, the dosage of ustekinumab is flexible. On the basis of the evidence, ustekinumab has a role in patients with primary failure or secondary loss of response to anti-tumor necrosis factor agents, as well as in those who have adverse events on front-line biologics or are reinitiating therapy after a treatment holiday. Current evidence suggests that ustekinumab may be particularly suitable in patients who present extra-intestinal manifestations of the disease or are at risk of infections. Ustekinumab may also be considered in the first-line setting, especially in frail patients, in young subjects or in those who have concomitant immune-mediated diseases.

摘要

这篇专家意见文章回顾了乌司奴单抗(一种人白细胞介素 12/23 单克隆抗体)在治疗克罗恩病中的应用的现有证据,并讨论了其在该疾病当前治疗方案中的潜在作用。乌司奴单抗似乎与临床研究计划中报告的快速和持续的临床效果相关,并有潜在的黏膜愈合支持。这些特征与良好的安全性概况、无免疫原性和存在全身抗炎活性相匹配。重要的是,乌司奴单抗只需单次静脉注射,随后通过皮下给药,这可能有利于家庭治疗。最后,乌司奴单抗的剂量具有灵活性。基于证据,乌司奴单抗在对抗肿瘤坏死因子药物原发性治疗失败或继发性失效的患者,以及在一线生物制剂治疗出现不良反应或治疗中断后重新开始治疗的患者中具有作用。目前的证据表明,乌司奴单抗可能特别适合有肠道外疾病表现或有感染风险的患者。乌司奴单抗也可以在一线治疗中考虑,特别是在体弱患者、年轻患者或同时患有免疫介导性疾病的患者中。

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