英夫利昔单抗和阿达木单抗中间抗抗体对克罗恩病或溃疡性结肠炎患者临床结局的影响

Chaoyang Wang, M. Tolaymat, R. Cross
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摘要

背景:抗肿瘤坏死因子药物阿达木单抗(ADA)和英夫利昔单抗(IFX)是治疗炎症性肠病(IBD)的有效药物。然而,40%的患者失去应答,通常是由于产生抗ada抗体(ATA)和抗ifx抗体(ATI)。虽然低ATA/ATI滴度(1,000 ng/mL)与较差的结果相关,但中等ATA/ATI滴度(200-999 ng/mL)的意义尚不清楚。本研究旨在探讨ATA/ATI中间滴度对IBD患者预后的影响。方法:对376例IBD患者进行回顾性分析。主要临床结果是在测量ATA/ATI滴度后抗tnf治疗持续1年。参与者包括2016年10月至2019年10月期间在马里兰大学医学中心炎症性肠病项目中接受IFX或ADA治疗的IBD患者。结果:在322例低滴度患者中,271例坚持原来的抗tnf,而15例中滴度患者中有9例(p=0.026), 10例高滴度患者中有1例(p<0.0001)。中间滴度与低滴度的持续优势比为0.26(0.09-0.80),高滴度与低滴度的持续优势比为0.02(0.00-0.14)。结论:中等滴度的患者比低滴度的患者更容易对抗tnf药物失去反应,需要改变抗tnf治疗。虽然中间滴度患者的样本量很小,但当存在中间滴度时,提供者应考虑抗tnf药物的剂量优化,无论是否添加免疫抑制剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Impact of Intermediate Antidrug Antibodies to Infliximab and Adalimumab on Clinical Outcomes in Patients with Crohn’s Disease or Ulcerative Colitis
Background: The anti-TNF drugs adalimumab (ADA) and infliximab (IFX) are effective treatments for inflammatory bowel disease (IBD). However, 40% of patients lose response, often due to the development of antibodies-to-ADA (ATA) and antibodies-to-IFX (ATI). While low ATA/ATI titres (<200 ng/mL) are associated with better outcomes and high ATA/ATI titres (>1,000 ng/mL) are associated with poorer outcomes, the significance of intermediate ATA/ATI titres (200–999 ng/mL) is not well understood. This study aims to investigate the impact of intermediate ATA/ATI titres on outcomes in patients with IBD. Methods: A retrospective chart review of 376 patients with IBD was conducted. The primary clinical outcome was persistence on anti-TNF therapy for 1 year after the measurement of ATA/ATI titres. The participants consisted of patients with IBD treated with IFX or ADA at the University of Maryland Medical Center’s Inflammatory Bowel Disease Program between October 2016 and October 2019. Results: Out of 322 patients with low titres, 271 persisted on their original anti-TNF, compared with nine out the 15 patients with intermediate titres (p=0.026) and one out the 10 patients with high titres (p<0.0001). The odds ratio of persistence when comparing intermediate titres to low titres was 0.26 (0.09–0.80), and when comparing high titres to low titres was 0.02 (0.00–0.14). Conclusion: Patients with intermediate titres were more likely to lose response to anti-TNF drugs and require a change in anti-TNF therapy than patients with low titres. Although the sample size of patients with intermediate titres was small, providers should consider dose optimisation of anti-TNF drugs, with or without the addition of an immunosuppressant, when intermediate titres are present.
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