Induction-phase infliximab monitoring accelerates time to remission in pediatric IBD: a retrospective cohort study.

IF 1.8 Q3 GASTROENTEROLOGY & HEPATOLOGY
Crohn's & Colitis 360 Pub Date : 2026-07-20 eCollection Date: 2026-07-01 DOI:10.1093/crocol/otag080
Nicholas Iovino, Samantha R Paglinco, Mahmoud Abdel-Rasoul, Megan McNicol, Brendan Boyle, Hilary K Michel, Ross M Maltz
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引用次数: 0

Abstract

Background: In pediatric inflammatory bowel disease (IBD), the optimal timing to begin therapeutic drug monitoring (TDM) of infliximab (IFX) is unclear. We hypothesized that TDM during induction of IFX improves clinical outcomes in children with IBD.

Methods: This retrospective cohort study utilized data from an internal database at Nationwide Children's Hospital between January 1, 2020, and December 31, 2023. Pediatric IBD patients receiving IFX with induction-phase TDM (I-TDM) at Week 6 were compared to those with maintenance-phase TDM (M-TDM) at Week 14. Propensity score matching (PSM) was used for sex, disease, and age at IFX start. The primary outcome was time to clinical remission.

Results: In total, 68 patients were matched from each group. The I-TDM group experienced a shorter median time to clinical remission (140 days [95% CI: 108, 167]) compared to the M-TDM group (203 days [95% CI: 167, 232]; P = .006). When adjusting for baseline variations, I-TDM remained independently associated with accelerated clinical remission (aHR = 1.68, 95% CI: 1.10, 2.55; P = .016). While time to therapeutic maintenance IFX levels was similar, post hoc analysis showed that 75% of patients in the I-TDM group achieved target levels in 134 days (95% CI: 114, 182) versus 183 days (95% CI: 153, 224) in the M-TDM group. There were no significant differences in long-term complications between the groups.

Conclusions: Induction-phase TDM before the third infusion shortens the time to clinical remission, allowing for more prompt dose adjustments and improving patient outcomes. This approach warrants consideration in clinical practice for children with IBD.

诱导期英夫利昔单抗监测加速儿童IBD缓解时间:一项回顾性队列研究。
背景:在儿童炎症性肠病(IBD)中,英夫利昔单抗(IFX)开始治疗药物监测(TDM)的最佳时机尚不清楚。我们假设在IFX诱导期间的TDM可以改善IBD患儿的临床结果。方法:这项回顾性队列研究利用了全国儿童医院2020年1月1日至2023年12月31日的内部数据库数据。在第6周接受IFX治疗的诱导期TDM (I-TDM)儿童IBD患者与在第14周接受IFX治疗的维持期TDM (M-TDM)儿童进行比较。倾向评分匹配(PSM)用于性别、疾病和IFX开始时的年龄。主要观察指标为临床缓解时间。结果:两组共匹配患者68例。与M-TDM组(203天[95% CI: 167, 232]; P = 0.006)相比,I-TDM组达到临床缓解的中位时间较短(140天[95% CI: 108, 167])。当调整基线变化时,I-TDM仍然与加速临床缓解独立相关(aHR = 1.68, 95% CI: 1.10, 2.55; P = 0.016)。虽然维持治疗性IFX水平的时间相似,但术后分析显示,I-TDM组中75%的患者在134天内达到目标水平(95% CI: 114,182),而M-TDM组为183天(95% CI: 153, 224)。两组间长期并发症发生率无显著差异。结论:第三次输注前的诱导期TDM缩短了临床缓解时间,允许更及时的剂量调整并改善患者预后。这种方法值得在IBD患儿的临床实践中加以考虑。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Crohn's & Colitis 360
Crohn's & Colitis 360 Medicine-Gastroenterology
CiteScore
2.50
自引率
0.00%
发文量
41
审稿时长
12 weeks
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