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加速递增英夫利昔单抗治疗与儿童克罗恩病的持续原发性缓解相关。

Accelerated Step-Up Infliximab Use Is Associated with Sustained Primary Response in Pediatric Crohn's Disease.

机构信息

Medical School, University of Western Australia, Crawley, WA, Australia.

Gastroenterology Department, Princess Margaret Hospital for Children, Perth, WA, Australia.

出版信息

Dig Dis Sci. 2018 Apr;63(4):1003-1010. doi: 10.1007/s10620-018-4969-8. Epub 2018 Feb 26.

Abstract

BACKGROUND

Earlier introduction of infliximab (IFX) in Crohn's disease (CD) may be associated with a sustained remission.

METHODS AND AIMS

Children on scheduled IFX therapy for predominant luminal CD after successful induction (drop in PCDAI by ≥ 15) and a minimum of 2-year IFX follow-up were included. We compared outcomes of children treated with early (within 3 months from diagnosis) versus later IFX (after failing conventional therapy ≥ 3 months) and identify clinical predictors of sustained primary response (SPR) in our cohort. SPR was defined as CS-free clinical remission without requiring IFX dose escalation and/or surgical excision and/or switch to second anti-TNFs due to LOR or allergic reaction.

RESULTS

Sixty-four children received IFX therapy for CD during the study period. Forty-three children on scheduled IFX therapy for luminal CD met the inclusion criteria. During the median follow-up of 3.05 years (IQR 2.6-3.5 years), SPR was observed in 17/43 (40%). SPR was associated with shorter time from diagnosis to the initiation of IFX (5.4 vs. 18.7 months, p = 0.006). Binary logistic regression using multiple variables also confirmed that only early use of IFX is associated with SPR.

CONCLUSION

Early step-up use of IFX in children with CD with inadequate clinical response to conventional therapies leads to sustained primary response over 2 years.

摘要

背景

在克罗恩病(CD)中更早地引入英夫利昔单抗(IFX)可能与持续缓解相关。

方法和目的

纳入了在成功诱导(PCDAI 下降≥15)后,按照计划接受 IFX 治疗以治疗主要腔内 CD 的儿童,并且有至少 2 年的 IFX 随访。我们比较了早期(诊断后 3 个月内)与晚期(在常规治疗失败≥3 个月后)接受 IFX 治疗的儿童的结局,并确定了我们队列中持续原发性反应(SPR)的临床预测因素。SPR 定义为无需 IFX 剂量增加和/或手术切除和/或由于 LOR 或过敏反应而转换为第二种抗 TNFs 即可实现无 IFX 剂量增加的临床缓解。

结果

在研究期间,64 名儿童接受了 IFX 治疗 CD。43 名按计划接受 IFX 治疗腔 CD 的儿童符合纳入标准。在中位数为 3.05 年(IQR 2.6-3.5 年)的随访期间,观察到 43 名儿童中有 17 名(40%)出现 SPR。SPR 与从诊断到开始 IFX 的时间较短相关(5.4 与 18.7 个月,p=0.006)。使用多个变量的二元逻辑回归也证实,仅早期使用 IFX 与 SPR 相关。

结论

在对常规治疗反应不足的 CD 儿童中早期逐步增加 IFX 的使用可在 2 年内实现持续的原发性反应。

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