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抗白细胞介素-1药物在风湿性疾病儿童中的长期安全性:一项系统评价。

Long-Term Safety of Anti-Interleukin-1 Medications in Children with Rheumatic Diseases: a Systematic Review.

作者信息

Isa M, Tiller G M, Liew D F L, Renton W D

机构信息

Department of Rheumatology, Northern Health, Melbourne, Australia.

Rheumatology Team, Department of General Medicine, The Royal Children's Hospital, Melbourne, Australia.

出版信息

Paediatr Drugs. 2025 Aug 20. doi: 10.1007/s40272-025-00712-7.

Abstract

BACKGROUND

Anti-interleukin-1 (IL-1) biologic disease-modifying anti-rheumatic drugs are the mainstay for several childhood rheumatic and autoinflammatory diseases. Long-term medication safety is a key consideration for chronic disease management.

AIM

The objective was to synthesise evidence on the long-term safety of anti-IL-1 medications in children and young people with rheumatic diseases, including autoinflammatory diseases.

METHODS

The study protocol was registered prospectively (PROSPERO CRD420251000272). Original full text studies of at least ten patients presenting safety data on anti-IL-1 medications in children with rheumatic diseases were eligible for inclusion. Medline, Embase and Web of Science were searched from inception to 27 February 2025. The methodological index for non-randomized studies (MINORS) tool was used to assess risk of bias. All relevant safety outcomes were presented and synthesised. Meta-analysis was not performed owing to study heterogeneity.

RESULTS

A total of 1660 unique records were screened, and 57 unique studies (3690 patients) were included. In total, 31 were retrospective cohort studies, and 10 were prospective interventional trials. Most studies were of moderate (n = 31) or high (n = 25) risk of bias. Rates of adverse events varied significantly between studies. Injection site reactions (particularly with anakinra) and minor infections were common. Infections were the most common type of serious adverse event. Drug reaction with eosinophilia and systemic symptoms (n = 3) and interstitial lung disease (including related conditions) (n = 9) were reported in patients with systemic onset juvenile arthritis only. Deaths (n = 16) and malignancies (n = 7) were uncommon, often occurring long after anti-IL-1 medication discontinuation and were often deemed to be unrelated to the anti-IL-1 medication.

CONCLUSIONS

Our results are consistent with the known safety profile of anti-IL-1 medications and show that they are generally safe for use in the context of childhood rheumatic and autoinflammatory diseases. This review of clinical trial and real-world data will help inform clinical decision-making and family counselling when initiating anti-IL-1 medications in children.

摘要

背景

抗白细胞介素-1(IL-1)生物性改善病情抗风湿药物是多种儿童风湿性和自身炎症性疾病的主要治疗药物。长期用药安全性是慢性病管理的关键考量因素。

目的

本研究旨在综合关于抗IL-1药物在患有风湿性疾病(包括自身炎症性疾病)的儿童和青少年中的长期安全性的证据。

方法

本研究方案已前瞻性注册(PROSPERO CRD420251000272)。纳入至少10例患者的关于抗IL-1药物在儿童风湿性疾病中的安全性数据的原始全文研究。检索了Medline、Embase和Web of Science数据库,检索时间从建库至2025年2月27日。使用非随机研究方法学指数(MINORS)工具评估偏倚风险。呈现并综合了所有相关的安全结局。由于研究的异质性,未进行荟萃分析。

结果

共筛选出1660条独特记录,纳入57项独特研究(3690例患者)。其中,31项为回顾性队列研究,10项为前瞻性干预试验。大多数研究的偏倚风险为中度(n = 31)或高度(n = 25)。不同研究之间不良事件发生率差异显著。注射部位反应(尤其是阿那白滞素)和轻度感染较为常见。感染是最常见的严重不良事件类型。仅在全身型幼年特发性关节炎患者中报告了药物性嗜酸性粒细胞增多和全身症状(n = 3)以及间质性肺疾病(包括相关病症)(n = 9)。死亡(n = 16)和恶性肿瘤(n = 7)并不常见,通常在停用抗IL-1药物很久之后发生,且通常被认为与抗IL-1药物无关。

结论

我们的结果与抗IL-1药物已知的安全性概况一致,表明它们在儿童风湿性和自身炎症性疾病中总体上使用安全。这项对临床试验和真实世界数据的综述将有助于在儿童开始使用抗IL-1药物时为临床决策和家庭咨询提供参考。

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