继发性反应丧失时阿达木单抗药物水平不能预测克罗恩病对剂量强化的反应:一项回顾性的国际多中心研究

IF 4.5 3区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY Inflammatory Bowel Diseases Pub Date : 2024-10-03 DOI:10.1093/ibd/izad248
Robert D Little, Adrian Swaine, Rebecca Reynolds, David J Gibson, Mathilde Barrau, Francesca D'Errico, Rumneek Hampal, Miles P Sparrow, Xavier Roblin, Peter M Irving, Mark G Ward
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引用次数: 0

摘要

背景:与英夫利昔单抗相比,阿达木单抗(ADA)在炎症性肠病(IBD)中的暴露-反应关系尚不明确。支持ADA剂量强化后治疗药物监测的证据有限。我们的目的是探讨ADA药物水平与克罗恩病(CD)活性在反应丧失时以及剂量强化后6个月和12个月之间的关系。方法:我们进行了一项回顾性研究,对5年内3个三级中心继发性反应丧失后接受剂量强化每周ADA治疗的成年CD患者进行了研究。使用药物敏感酶联免疫吸附法分析ADA谷水平,在反应丧失和剂量增强后6个月和12个月。临床缓解率、客观缓解率(c反应蛋白)结果:共纳入131例CD患者,中位病程为9年(四分位数范围4-17年)。51%的人在ADA之前有生物暴露,50%的人同时接受了免疫调节剂。在继发性反应丧失时测量的基线药物水平在剂量强化后6个月或12个月对随后的反应者和无反应者没有区别。然而,在6个月和12个月时较高的药物水平和较基线的较高增量与改善的结果相关。在受体工作特征分析中,升级后ADA药物水平>为10.7µg/mL(受体工作特征曲线下面积[AUROC], 0.66;P = 0.013)和>10.9µg/mL (AUROC, 0.67;P = 0.032)分别与6个月和12个月的客观缓解相关。结论:剂量强化后的药物水平与随后的CD缓解相关,而不是继发性反应丧失时的药物水平。
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Adalimumab Drug Levels at Secondary Loss of Response Do Not Predict Response to Dose-intensification in Crohn's Disease: A Retrospective, International Multicenter Study.

Background: The exposure-response relationship is less established for adalimumab (ADA) compared with infliximab in inflammatory bowel disease (IBD). Evidence supporting therapeutic drug monitoring post dose-intensification of ADA is limited. We aimed to explore the association between ADA drug levels and Crohn's disease (CD) activity at loss of response, and at 6 and 12 months post dose-intensification.

Methods: We performed a retrospective study of adult patients with CD receiving dose-intensified weekly ADA following secondary loss of response at 3 tertiary centers across 5 years. ADA trough levels were analyzed using a drug-sensitive enzyme-linked immunosorbent assay at loss of response, and 6 and 12 months after dose-intensification. Rates of clinical remission, objective remission (C-reactive protein <5 mg/L, fecal calprotectin <150 µg/g, or absence of inflammation at endoscopy or imaging), and ADA failure were investigated.

Results: A total of 131 CD patients were included, with a median disease duration of 9 (interquartile range, 4-17) years. 51% were biologic exposed prior to ADA and 50% received concomitant immunomodulators. Baseline drug levels measured at secondary loss of response did not discriminate between subsequent responders and non-responders at either 6 or 12 months post dose-intensification. However, both higher drug levels at 6 and 12 months and a higher increment from baseline were associated with improved outcomes. On receiver-operating characteristic analyses, post-escalation ADA drug levels >10.7 µg/mL (area under the receiver-operating characteristic curve [AUROC], 0.66; P = .013) and >10.9 µg/mL (AUROC, 0.67; P = .032) were associated with objective remission at 6 and 12 months, respectively.

Conclusions: Drug levels following dose-intensification rather than at the time of secondary loss of response were associated with subsequent CD remission.

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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.
期刊最新文献
Reply: MIND the Gap: Psychiatric Conditions in Inflammatory Bowel Disease. Inflammatory Bowel Disease in Adults and Elderly: The Use of Selected Non-IBD Medication Examined in a Nationwide Cohort Study. Proactive Infliximab Monitoring Improves the Rates of Transmural Remission in Crohn's Disease: A Propensity Score-Matched Analysis. Clusters of Disease Activity and Early Risk Factors of Clinical Course of Pediatric Crohn's Disease. Automatic Segmentation and Radiomics for Identification and Activity Assessment of CTE Lesions in Crohn's Disease.
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