Efficacy and safety of tumor necrosis factor inhibitors for systemic juvenile idiopathic arthritis: a systematic review.

IF 1.8 4区 医学 Q3 RHEUMATOLOGY
Takashi Ishikawa, Kenichi Nishimura, Nami Okamoto, Keiji Akamine, Natsumi Inoue, Hitoshi Irabu, Kentaro Kato, Hiroshi Keino, Masayo Kojima, Hiroshi Kubo, Kazuichi Maruyama, Mao Mizuta, Kosuke Shabana, Masaki Shimizu, Yuko Sugita, Yukiko Takakuwa, Satoshi Takanashi, Hiroshi Takase, Hiroaki Umebayashi, Natsuka Umezawa, Shingo Yamanishi, Kazuko Yamazaki, Masato Yashiro, Takahiro Yasumi, Masaaki Mori
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引用次数: 0

Abstract

Objectives: This systematic review assessed the efficacy and safety of tumor necrosis factor (TNF) inhibitors in patients with systemic juvenile idiopathic arthritis (JIA).

Methods: Studies were searched using PubMed, Embase, Cochrane, Ichushi-Web, and clinical trial registries (from 2000 to 2021). The risk of bias was assessed using the Cochrane Risk of Bias version 2 for randomized controlled trials (RCTs) and the manual for development clinical practice guidelines by Minds, a project promoting evidence-based medicine in Japan, for observational studies.

Results: One RCT and 22 observational studies were included. In the RCT on infliximab, the American College of Rheumatology pediatric (ACR Pedi) 30/50/70 responses at 14 weeks were 63.8%/50.0%/22.4%, with relative risks of 1.30 (95% confidence interval [CI]: 0.94-1.79)/1.48 (95% CI: 0.95-2.29)/1.89 (95% CI: 0.81-4.40), respectively. In the observational studies, ACR Pedi 30/50/70 responses for etanercept at 12 months were 76.7%/64.7%/46.4%, respectively. Infliximab treatment caused anaphylaxis in 17% and an infusion reaction in 23% of patients. The incidence of macrophage activation syndrome, serious infection and malignancy caused by TNF inhibitors was 0%-4%.

Conclusions: Thus, although TNF inhibitors were relatively safe, they were unlikely to be preferentially administered in patients with systemic JIA because of their inadequate efficacy. Further studies, particularly well-designed RCTs, are necessary to confirm the efficacy and safety of TNF inhibitors for systemic JIA.

肿瘤坏死因子抑制剂治疗全身性幼年特发性关节炎的有效性和安全性:系统性综述。
目的:本系统综述评估了肿瘤坏死因子(TNF)抑制剂对全身性幼年特发性关节炎(JIA)患者的疗效和安全性:本系统综述评估了肿瘤坏死因子(TNF)抑制剂对全身性幼年特发性关节炎(JIA)患者的疗效和安全性:通过PubMed、Embase、Cochrane、Ichushi-Web和临床试验登记(2000年至2021年)检索研究。对随机对照试验(RCT)采用 Cochrane Risk of Bias version 2 评估偏倚风险,对观察性研究采用日本循证医学推广项目 Minds 的临床实践指南制定手册评估偏倚风险:结果:共纳入了 1 项随机对照试验和 22 项观察性研究。在关于英夫利西单抗的研究中,14周时美国风湿病学会儿科(ACR Pedi)30/50/70应答率分别为63.8%/50.0%/22.4%,相对风险分别为1.30(95%置信区间[CI]:0.94-1.79)/1.48(95% CI:0.95-2.29)/1.89(95% CI:0.81-4.40)。在观察性研究中,依那西普治疗12个月后的ACR Pedi 30/50/70反应率分别为76.7%/64.7%/46.4%。英夫利西单抗治疗导致17%的患者出现过敏性休克,23%的患者出现输液反应。TNF抑制剂导致的巨噬细胞活化综合征、严重感染和恶性肿瘤的发生率为0%-4%:因此,尽管TNF抑制剂相对安全,但由于其疗效不佳,不可能优先用于全身性JIA患者。要确认TNF抑制剂对全身性JIA的疗效和安全性,还需要进一步的研究,尤其是精心设计的RCT研究。
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来源期刊
Modern Rheumatology
Modern Rheumatology RHEUMATOLOGY-
CiteScore
4.90
自引率
9.10%
发文量
146
审稿时长
1.5 months
期刊介绍: Modern Rheumatology publishes original papers in English on research pertinent to rheumatology and associated areas such as pathology, physiology, clinical immunology, microbiology, biochemistry, experimental animal models, pharmacology, and orthopedic surgery. Occasional reviews of topics which may be of wide interest to the readership will be accepted. In addition, concise papers of special scientific importance that represent definitive and original studies will be considered. Modern Rheumatology is currently indexed in Science Citation Index Expanded (SciSearch), Journal Citation Reports/Science Edition, PubMed/Medline, SCOPUS, EMBASE, Chemical Abstracts Service (CAS), Google Scholar, EBSCO, CSA, Academic OneFile, Current Abstracts, Elsevier Biobase, Gale, Health Reference Center Academic, OCLC, SCImago, Summon by Serial Solutions
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