Lowell Jeffrey A, Sharma Garvita, Chua Vincent, Ben-Horin Shomron, Swaminath Arun, Sultan Keith
Department of Medicine, Zucker School of Medicine at Hofstra/Northwell, Northwell Health, Manhasset, NY, 11030, USA.
, 300 Community Drive, Manhasset, NY, 11030, USA.
Dig Dis Sci. 2024 Oct;69(10):3920-3931. doi: 10.1007/s10620-024-08515-5. Epub 2024 Jun 14.
Patients with inflammatory bowel disease (IBD) receiving infliximab (IFX) commonly experience immunogenic loss of response (LOR) by formation of anti-drug antibodies (ADAs). An immunomodulator (IMM) used in combination with initial IFX induction is known to reduce ADA development and improve clinical outcomes. We aimed to assess the impact of reactively adding an IMM to patients on IFX monotherapy.
We conducted a retrospective cohort study and systematic review with meta-analysis of patients with IBD demonstrating immunologic LOR, with or without clinical LOR, that had an IMM (azathioprine, 6-mercaptopurine, or methotrexate) reactively added (reactive combination therapy; rCT) to combat elevated ADAs and raise IFX level. Data were extracted for pooled effect size estimation using random-effects models, and ADA and IFX trough levels were compared pre- and post-IMM initiation.
We identified 6 patients who received rCT due to rising ADA titers and low IFX levels. Median ADA titer decreased from 506 ng/mL (interquartile range (IQR) [416-750]) to 76.5 ng/mL (IQR [25.8-232]), an 85% decrease (p = 0.031). Median IFX trough increased from 0.4 µg/mL (IQR [0.4-0.48]) to 8.25 µg/mL (IQR [3.7-9.6]), a 20.6-fold increase (p = 0.038). Meta-analysis pooled effect size of 7 studies with 89 patients showed an 87% ADA titer reduction [95% confidence interval (CI) = 72-94%], 6.7-fold increased IFX trough (95% CI = 2.4-18.7), and 76% clinical remission rescue rate (95% CI = 59-93%).
These results suggest rCT is a valid rescue strategy in patients with immunogenic LOR to IFX to reduce ADA titers, restore therapeutic IFX levels, and recapture clinical remission of IBD.
接受英夫利昔单抗(IFX)治疗的炎症性肠病(IBD)患者通常会因形成抗药物抗体(ADA)而出现免疫原性反应丧失(LOR)。已知与初始IFX诱导联合使用的免疫调节剂(IMM)可减少ADA的产生并改善临床结局。我们旨在评估在接受IFX单药治疗的患者中反应性添加IMM的影响。
我们进行了一项回顾性队列研究,并对显示有免疫性LOR(无论有无临床LOR)的IBD患者进行了系统评价和荟萃分析,这些患者反应性添加了IMM(硫唑嘌呤、6-巯基嘌呤或甲氨蝶呤)以对抗升高的ADA并提高IFX水平。使用随机效应模型提取数据以估计合并效应量,并比较IMM开始前后的ADA和IFX谷值水平。
我们确定了6例因ADA滴度升高和IFX水平低而接受反应性联合治疗(rCT)的患者。ADA滴度中位数从506 ng/mL(四分位间距(IQR)[416 - 7