Long-term Outcomes of Patients with Crohn's Disease Treated with Risankizumab.

IF 4.3 3区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY
Grace Geeganage, Ajay Gade, Alessandra Saraga, Tina Deyhim, Samantha Zullow, Loren G Rabinowitz, Adam S Cheifetz, Laurie B Grossberg, Konstantinos Papamichael
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引用次数: 0

Abstract

Background: Cumulative data suggest that risankizumab is an effective and safe treatment for patients with Crohn's disease (CD). However, most of the data derive from randomized controlled trials or small retrospective studies with short- or mid-term follow-up. This study aimed to assess the long-term effectiveness and safety of risankizumab in a real-world cohort of patients with CD.

Methods: This single-center, retrospective, cohort study included consecutive patients with CD treated with risankizumab from October 2022 to August 2024. A time-to-event analysis was performed for treatment failure, treatment escalation, and CD-related health care utilization. Treatment failure was defined as the need for drug discontinuation due to primary nonresponse, loss of response, or a serious adverse event or the need for IBD (inflammatory bowel disease)-related surgery. Treatment escalation was defined as the need for shortening the dose interval or intravenous reinduction due to breakthrough CD-related symptoms and/or elevated biomarkers, such as C-reactive protein and fecal calprotectin. Health care utilization was defined as CD-related emergency department visit or hospitalization. Patients were followed from start of risankizumab until drug discontinuation or the end of follow-up (October 2024).

Results: The study population consisted of 106 patients with CD (74% receiving prior biological therapies). Patients were followed for a median of 12 [interquartile range (IQR), 6.8-18.8] months; 14 (13%) patients had treatment failure; 24 (23%) had treatment escalation; and 17 (16%) had CD-related health care utilization. Multivariable Cox proportional hazards regression analysis identified penetrating CD as associated with treatment failure [hazard ratio (HR), 5.2; 95% confidence interval (CI), 1.6-17.2; P = .007], while perianal fistulizing CD (HR, 3.3; 95% CI, 1.2-9.4; P = .023) and prior exposure to more than 2 biologics (HR, 5.8; 95% CI, 1.3-26.3; P = .022) were associated with treatment escalation.

Conclusion: In this real-world cohort with long-term follow-up, risankizumab was generally effective in patients with CD. Penetrating CD was associated with treatment failure, while perianal fistulizing CD and prior exposure to more than 2 biologics were associated with treatment escalation.

利桑单抗治疗克罗恩病患者的长期预后
背景:累积数据表明,risankizumab是克罗恩病(CD)患者有效且安全的治疗方法。然而,大多数数据来自随机对照试验或短期或中期随访的小型回顾性研究。该研究旨在评估利桑单抗在现实世界CD患者队列中的长期有效性和安全性。方法:这项单中心、回顾性、队列研究纳入了2022年10月至2024年8月期间连续接受利桑单抗治疗的CD患者。对治疗失败、治疗升级和cd相关的医疗保健利用进行了时间到事件的分析。治疗失败被定义为由于原发性无反应、反应丧失、严重不良事件或需要进行炎症性肠病相关手术而需要停药。治疗升级被定义为由于cd相关症状的突破和/或生物标志物(如c反应蛋白和粪便钙保护蛋白)升高而需要缩短剂量间隔或静脉重新诱导。医疗保健利用被定义为与cd相关的急诊就诊或住院。患者从利桑单抗开始随访至停药或随访结束(2024年10月)。结果:研究人群包括106例CD患者(74%接受过生物治疗)。患者随访时间中位数为12个月[四分位数间距(IQR), 6.8-18.8]个月;14例(13%)患者治疗失败;治疗升级24例(23%);17人(16%)有cd相关的医疗保健利用。多变量Cox比例风险回归分析发现,穿透性CD与治疗失败相关[风险比(HR), 5.2;95%置信区间(CI), 1.6-17.2;p =。[007],而肛周瘘CD (HR, 3.3; 95% CI, 1.2 ~ 9.4; P =。023)和之前暴露于2种以上的生物制剂(HR, 5.8; 95% CI, 1.3-26.3; P =。022)与治疗升级相关。结论:在这个长期随访的现实世界队列中,利桑单抗对CD患者普遍有效。穿透性CD与治疗失败相关,而肛周瘘管性CD和先前暴露于2种以上生物制剂与治疗升级相关。
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来源期刊
Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 医学-胃肠肝病学
CiteScore
9.70
自引率
6.10%
发文量
462
审稿时长
1 months
期刊介绍: Inflammatory Bowel Diseases® supports the mission of the Crohn''s & Colitis Foundation by bringing the most impactful and cutting edge clinical topics and research findings related to inflammatory bowel diseases to clinicians and researchers working in IBD and related fields. The Journal is committed to publishing on innovative topics that influence the future of clinical care, treatment, and research.
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