Department of Gastroenterology, Nancy University Hospital, Vandœuvre-lès-Nancy, France.
INSERM, NGERE, University of Lorraine, Nancy, France.
United European Gastroenterol J. 2024 Jun;12(5):605-613. doi: 10.1002/ueg2.12547. Epub 2024 Apr 9.
Many patients with inflammatory bowel disease (IBD) have signs or symptoms of active disease despite multiple treatment attempts. This emerging concept is defined as difficult-to-treat IBD.
The objective of this study was to investigate for the first time the treatment persistence, efficacy and safety of biologics or small molecules used in 4th or 5th line therapy.
We reviewed all consecutive patients with IBD treated at the Nancy University Hospital between July 2022 and April 2023 with the 4th or 5th line treatment for at least three months. The primary outcome was to assess the persistence rate of 4th and 5th line therapy.
We enrolled 82 patients with IBD (4th line: 44; 5th line: 38). On Kaplan-Meier analysis, the duration of risankizumab, ustekinumab or vedolizumab therapy did not differ significantly (p > 0.05) as 4th and 5th line treatment. The restricted mean survival time analysis showed that the persistence rate of risankizumab was the highest as 4th line therapy (risankizumab vs. vedolizumab: 36.0 and 29.4 weeks, respectively, p = 0.008; risankizumab vs. ustekinumab: 36.0 and 32.8 weeks, respectively, p = 0.035). In multivariate regression, Crohn's disease diagnosis (Odd ratio 4.6; 95% confidence interval 1.7-12.4) was significantly associated with treatment persistence.
In this first real-world setting, risankizumab could have a longer persistence rate as 4th line treatment for IBD than other agents. Persistence of biological agents was greater in Crohn's disease than in ulcerative colitis. More studies are needed to compare treatment efficacy in patients with difficult-to-treat IBD.
尽管进行了多次治疗尝试,许多炎症性肠病(IBD)患者仍存在疾病活动的迹象或症状。这种新出现的概念被定义为难治性 IBD。
本研究旨在首次调查生物制剂或小分子药物在第 4 或 5 线治疗中的治疗持久性、疗效和安全性。
我们回顾了 2022 年 7 月至 2023 年 4 月期间在南锡大学医院接受第 4 或 5 线治疗至少 3 个月的所有连续 IBD 患者。主要结局是评估第 4 线和第 5 线治疗的持续率。
我们纳入了 82 例 IBD 患者(第 4 线:44 例;第 5 线:38 例)。在 Kaplan-Meier 分析中,利纳西珠单抗、乌司奴单抗或维得利珠单抗治疗的持续时间无显著差异(p>0.05),均作为第 4 线和第 5 线治疗。限制平均生存时间分析显示,利纳西珠单抗作为第 4 线治疗的持续率最高(利纳西珠单抗与维得利珠单抗:36.0 和 29.4 周,分别,p=0.008;利纳西珠单抗与乌司奴单抗:36.0 和 32.8 周,分别,p=0.035)。在多变量回归中,克罗恩病诊断(比值比 4.6;95%置信区间 1.7-12.4)与治疗持续时间显著相关。
在这一真实世界环境中,利纳西珠单抗作为 IBD 的第 4 线治疗药物,其持续率可能高于其他药物。在克罗恩病中,生物制剂的持续时间长于溃疡性结肠炎。需要更多的研究来比较难治性 IBD 患者的治疗效果。