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英夫利昔单抗治疗儿童克罗恩病的短期疗效:单中心经验

Short-Term Outcome of Infliximab Therapy in Pediatric Crohn's Disease: A Single-Center Experience.

作者信息

Jung Dai, Lee Sunghee, Jeong Insook, Oh Seak Hee, Kim Kyung Mo

机构信息

Department of Pediatrics, Asan Medical Center Children's Hospital, University of Ulsan College of Medicine, Seoul, Korea.

出版信息

Pediatr Gastroenterol Hepatol Nutr. 2017 Dec;20(4):236-243. doi: 10.5223/pghn.2017.20.4.236. Epub 2017 Dec 22.

Abstract

PURPOSE

Studies on the efficacy of infliximab (IFX) in a large population of pediatric patients with Crohn's disease (CD) are limited, and prognostic factors are not well-known. The aim of this study was to evaluate outcomes of IFX in pediatric patients with CD and to identify factors associated with poor prognosis.

METHODS

We retrospectively analyzed medical data of 594 pediatric patients with CD between 1987 and 2013 in a tertiary center. Of these, 156 children treated with IFX were enrolled and were followed up for at least a year with intact data. Outcomes of induction and maintenance, classified as failure or clinical response, were evaluated on the tenth and 54th week of IFX therapy.

RESULTS

We treated 156 pediatric patients with CD with IFX, and the median duration of IFX therapy was 47 months. For IFX induction therapy, 134 (85.9%) patients experienced clinical response on the 10th week. Among the 134 patients who showed response to induction, 111 (82.8%) patients maintained the clinical response on the 54th week. In multivariate analysis, low hematocrit (=0.046) at the time of IFX initiation was associated with the failure of IFX induction. For IFX maintenance therapy, longer duration from the initial diagnosis to IFX therapy (=0.017) was associated with maintenance failure on the 54th week.

CONCLUSION

We have shown the acceptable outcomes of IFX in a large cohort of pediatric CD patients in Korea. Hematocrit and early introduction of IFX may be prognostic factors for the outcomes of IFX.

摘要

目的

关于英夫利昔单抗(IFX)在大量儿童克罗恩病(CD)患者中的疗效研究有限,且预后因素尚不明确。本研究旨在评估IFX在儿童CD患者中的治疗效果,并确定与预后不良相关的因素。

方法

我们回顾性分析了1987年至2013年在一家三级中心就诊的594例儿童CD患者的医疗数据。其中,156例接受IFX治疗的儿童被纳入研究,并对其进行了至少一年的随访,数据完整。在IFX治疗的第10周和第54周,评估诱导和维持治疗的结果,分为治疗失败或临床缓解。

结果

我们用IFX治疗了156例儿童CD患者,IFX治疗的中位持续时间为47个月。对于IFX诱导治疗,134例(85.9%)患者在第10周出现临床缓解。在134例诱导治疗有反应的患者中,111例(82.8%)患者在第54周维持了临床缓解。多因素分析显示,开始IFX治疗时低血细胞比容(=0.046)与IFX诱导治疗失败相关。对于IFX维持治疗,从初始诊断到开始IFX治疗的时间较长(=0.017)与第54周维持治疗失败相关。

结论

我们已证明IFX在韩国大量儿童CD患者中的治疗效果良好。血细胞比容和IFX的早期应用可能是IFX治疗效果的预后因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b575/5750378/2bd7188216fa/pghn-20-236-g001.jpg

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