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乌司奴单抗治疗儿童炎症性肠病的有效性和安全性:系统评价。

Effectiveness and Safety of Ustekinumab for Pediatric Inflammatory Bowel Disease: A Systematic Review.

机构信息

Department of Clinical Pharmacy, First Hospital of Jilin University, 71 Xinmin Street, Changchun, 130021, Jilin, China.

Department of Pediatric Gastroenterology Unit, First Hospital of Jilin University, Changchun, China.

出版信息

Paediatr Drugs. 2023 Sep;25(5):499-513. doi: 10.1007/s40272-023-00586-7. Epub 2023 Aug 1.

Abstract

BACKGROUND

The use of ustekinumab in pediatric patients with inflammatory bowel disease (IBD) is off-label and the data are limited. We conducted a systematic review evaluating the efficacy and safety of ustekinumab in pediatric IBD.

METHODS

We systematically searched PubMed, EMBASE and Cochrane databases for studies of ustekinumab in children and adolescents with IBD investigating clinical remission, clinical response, corticosteroid-free (CS-free) remission, endoscopic remission/response, or safety up to March 17, 2023. A random-effects model was used for calculating summary estimates.

RESULTS

Eleven studies, comprising 370 patients were included. For Crohn's disease (CD), the pooled clinical remission rates were 34% (73/204) at 8-16 weeks and 46% (60/129) at 1 year. The pooled CS-free clinical remission rates were 23% (10/44) at 8-16 weeks and 45% (42/96) at 1 year. For ulcerative colitis (UC)/IBD unspecified (IBD-U), the pooled CS-free clinical remission rates were 24% (6/25) at 26 weeks and 46% (16/35) at 1 year. Endoscopic remission was found in 0-37.5% of CD and 63.6% of UC. Serious adverse events were reported in 3.5% of patients. About one half of patients required reduction in dose intervals and 62.75% patients could continue ustekinumab therapy at 1 year or final visit.

CONCLUSIONS

According to low-quality evidence mainly from cohort studies and case series, approximately one half of patients with CD and UC/IBD-U achieved remission at 1 year. Ustekinumab has a reasonable safety profile and dose optimization is frequently required. Data on the long-term benefit and high-quality evidence are still needed.

摘要

背景

乌司奴单抗在炎症性肠病(IBD)儿科患者中的使用属于超适应证用药,且相关数据有限。我们进行了一项系统评价,旨在评估乌司奴单抗治疗儿科 IBD 的疗效和安全性。

方法

我们系统地检索了 PubMed、EMBASE 和 Cochrane 数据库,以获取截至 2023 年 3 月 17 日有关乌司奴单抗治疗儿童和青少年 IBD 的研究,评估临床缓解、临床应答、无皮质类固醇缓解、内镜缓解/应答或安全性。采用随机效应模型计算汇总估计值。

结果

共纳入 11 项研究,包括 370 例患者。对于克罗恩病(CD),8-16 周时的汇总临床缓解率为 34%(73/204),1 年时为 46%(60/129)。8-16 周时的汇总无皮质类固醇临床缓解率为 23%(10/44),1 年时为 45%(42/96)。对于溃疡性结肠炎(UC)/未特指的 IBD(IBD-U),26 周时的汇总无皮质类固醇临床缓解率为 24%(6/25),1 年时为 46%(16/35)。CD 患者内镜缓解率为 0-37.5%,UC 患者为 63.6%。报告了 3.5%的患者出现严重不良事件。约有一半的患者需要减少剂量间隔,62.75%的患者在 1 年或最后一次就诊时可以继续接受乌司奴单抗治疗。

结论

根据主要来自队列研究和病例系列研究的低质量证据,约有一半的 CD 和 UC/IBD-U 患者在 1 年内达到缓解。乌司奴单抗具有合理的安全性特征,经常需要进行剂量优化。仍需要长期获益和高质量证据的数据。

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