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肿瘤坏死因子-α拮抗剂治疗小儿克罗恩病的长期疗效。

Long-term outcome of tumor necrosis factor alpha antagonist's treatment in pediatric Crohn's disease.

机构信息

Institute of Gastroenterology, Nutrition and Liver Disease, Schneider Children's Medical Center, Petach-Tikva, Israel.

出版信息

J Crohns Colitis. 2013 Jun;7(5):369-76. doi: 10.1016/j.crohns.2012.03.006. Epub 2012 Apr 5.

Abstract

BACKGROUND

Anti tumor necrosis factor alpha (TNFα) agents have become widely used in pediatric inflammatory bowel disease (IBD). So far, only few studies examined the long-term results of anti-TNFα treatment in children with IBD.

METHODS

The long-term outcome of pediatric patients with IBD was assessed retrospectively in a multicenter cohort of children treated with anti-TNFα beyond induction treatment. Short- and long-term response rates, predictors for loss of response, data on growth and laboratory parameters were assessed.

RESULTS

120 patients [101 crohn's disease (CD), 19 ulcerative colitis (UC) or indeterminate colitis (IC)] received either infliximab or adalimumab. The mean age at initiation of anti-TNFα was 13.4 ± 3.9 years and the median duration of anti-TNFα treatment was 15 months (range: 2-90). Overall, 89% of the cohort experienced short-term response following induction. Response was associated with improvement in weight and BMI Z-scores (p<0.001) but not with linear growth. Responders experienced a significant decrease in erythrocyte sedimentation rate (ESR) and C reactive protein (CRP) during treatment (p<0.001). Albumin and hemoglobin both improved but only albumin increased significantly (p<0.001). The cumulative probability of losing response to anti-TNFα treatment was 17%, 38%, and 49% after 1, 3, and 5 years, respectively. Responders had a significantly lower weight and BMI Z-scores at initiation of anti-TNFα treatment in compared to non-responders (p=0.04 and 0.02 respectively).

CONCLUSIONS

Our long term cohort supports the current evidence on the effectiveness and safety of anti-TNFα treatment in children with IBD. Response to treatment was interestingly associated with lower weight and BMI.

摘要

背景

抗肿瘤坏死因子 α(TNFα)药物已广泛应用于儿科炎症性肠病(IBD)。迄今为止,仅有少数研究检查了抗 TNFα 治疗在儿童 IBD 中的长期结果。

方法

通过对接受抗 TNFα 诱导治疗后长期治疗的儿科患者进行多中心队列回顾性研究,评估 IBD 患儿的长期结果。评估短期和长期反应率、反应丧失的预测因素、生长和实验室参数的数据。

结果

120 例患者[101 例克罗恩病(CD)、19 例溃疡性结肠炎(UC)或不确定结肠炎(IC)]接受英夫利昔单抗或阿达木单抗治疗。抗 TNFα 起始年龄的平均年龄为 13.4±3.9 岁,抗 TNFα 治疗的中位数时间为 15 个月(范围:2-90)。总体而言,89%的患者在诱导后有短期反应。反应与体重和 BMI Z 评分的改善相关(p<0.001),但与线性生长无关。反应者在治疗过程中红细胞沉降率(ESR)和 C 反应蛋白(CRP)显著下降(p<0.001)。白蛋白和血红蛋白均改善,但仅白蛋白显著增加(p<0.001)。抗 TNFα 治疗后 1、3 和 5 年,失去反应的累积概率分别为 17%、38%和 49%。与无反应者相比,反应者在开始抗 TNFα 治疗时的体重和 BMI Z 评分明显较低(分别为 p=0.04 和 0.02)。

结论

我们的长期队列支持目前关于抗 TNFα 治疗儿童 IBD 的有效性和安全性的证据。治疗反应与较低的体重和 BMI 相关。

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