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英夫利昔单抗谷浓度较高与炎症性肠病患儿的预后改善相关。

Higher Infliximab Trough Levels Are Associated With Better Outcome in Paediatric Patients With Inflammatory Bowel Disease.

机构信息

Department of Paediatric Gastroenterology & Hepatology & Nutrition, University Hospitals Leuven, KU Leuven, Leuven, Belgium.

TARGID, Department of Chronic Diseases, Metabolism and Ageing [CHROMETA], KU Leuven, Leuven, Belgium.

出版信息

J Crohns Colitis. 2018 Nov 15;12(11):1316-1325. doi: 10.1093/ecco-jcc/jjy111.

Abstract

BACKGROUND

The role of therapeutic drug monitoring for infliximab [IFX] therapy in children with inflammatory bowel disease [IBD] is poorly investigated. We determined if IFX exposure correlates with long-term remission in children.

METHODS

In this retrospective study, all children with Crohn's disease [CD] and ulcerative colitis [UC], receiving maintenance IFX at our centre, were included. Serum trough levels and cumulative drug exposure were correlated with clinical, biological, and endoscopic remission. All children received proactive drug monitoring and dose adaptation aiming to target a therapeutic window of 3-7 µg/mL. All data are presented as median [interquartile range].

RESULTS

A total of 686 serum levels during IFX maintenance in 52 paediatric patients [33 CD and 19 UC] were included (median 9 [4-18] per patient). With a median of 17 [8-36] months under IFX therapy, 39/52 [75%] patients were in clinical remission and 29/40 [73%] patients were in endoscopic remission. Median IFX trough levels were significantly higher when children achieved clinical remission (5.4 [3.8-8.0] µg/mL versus 4.2 [2.6-6.7] µg/mL), biological remission (5.2 [3.7-7.7] µg/mL versus 4.2 [2.6-6.5] µg/mL), combined clinical and biological remission (5.7 [4.0-8.2] µg/mL versus 4.4 [2.7-6.8] µg/mL) and endoscopic remission (6.5 [4.2-9.5] µg/mL versus 3.2 [2.3-5.6] µg/mL) compared with not meeting these criteria [all p ≤ 0.001].

CONCLUSIONS

In this large paediatric cohort, children with clinical and/or endoscopic remission had significantly higher IFX exposure during maintenance therapy. We showed excellent outcome data using serial and systematic measurements of drug levels. This could provide a rationale for the use of proactive drug monitoring in children in order to improve long-term outcomes.

摘要

背景

英夫利昔单抗(IFX)治疗炎症性肠病(IBD)患儿的治疗药物监测作用尚未得到充分研究。我们旨在确定 IFX 暴露是否与儿童的长期缓解相关。

方法

在这项回顾性研究中,纳入了在我院接受维持性 IFX 治疗的所有克罗恩病(CD)和溃疡性结肠炎(UC)患儿。血清谷浓度和累积药物暴露与临床、生物学和内镜缓解相关。所有患儿均接受主动药物监测和剂量调整,以达到 3-7μg/ml 的治疗窗。所有数据均以中位数(四分位数范围)表示。

结果

纳入了 52 例患儿(33 例 CD 和 19 例 UC)在接受 IFX 维持治疗期间的 686 份血清样本(中位数每个患儿 9 [4-18] 份)。在 IFX 治疗中位数为 17 [8-36] 个月的情况下,52 例患儿中有 39 例(75%)达到临床缓解,40 例患儿中有 29 例(73%)达到内镜缓解。与未达到这些标准的患儿相比,达到临床缓解(5.4 [3.8-8.0]μg/ml 与 4.2 [2.6-6.7]μg/ml)、生物学缓解(5.2 [3.7-7.7]μg/ml 与 4.2 [2.6-6.5]μg/ml)、联合临床和生物学缓解(5.7 [4.0-8.2]μg/ml 与 4.4 [2.7-6.8]μg/ml)和内镜缓解(6.5 [4.2-9.5]μg/ml 与 3.2 [2.3-5.6]μg/ml)的患儿 IFX 谷浓度显著更高(所有 p≤0.001)。

结论

在这项大型儿科队列研究中,达到临床和/或内镜缓解的患儿在维持治疗期间 IFX 暴露显著更高。我们通过对药物水平进行连续和系统的测量,提供了出色的结果数据。这为在儿童中使用主动药物监测以改善长期结局提供了依据。

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