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儿童丙型肝炎的治疗:系统评价。

Treatment of hepatitis C in children: a systematic review.

机构信息

Department of Pediatrics, University of Alberta, Edmonton, Canada.

出版信息

PLoS One. 2010 Jul 13;5(7):e11542. doi: 10.1371/journal.pone.0011542.

Abstract

BACKGROUND

Current guidelines recommend children be treated for hepatitis C virus (HCV) using the same principles applied in adults. There are however few published studies which assess the efficacy and safety of HCV therapy in children.

METHODOLOGY/PRINCIPAL FINDINGS: A systematic review of the literature was completed for studies of any design that evaluated HCV therapy in children. The primary outcome was sustained virologic response (SVR), with sub-group analysis of response rates by genotype. There were 4 randomized controlled trials (RCTs) and 31 non-randomized studies, all involving interferon, pegylated interferon (PEG-IFN), or combinations of these drugs with ribavirin. The SVR rate could not be directly compared as the populations and interventions differed across studies. Genotype was not reported or differed substantially from study to study. The overall SVR rate for PEG-IFN and ribavirin ranged from 30 to 100% which is comparable to the rate in adults. Similar to adults, the SVR rates were significantly higher in children with genotype 2 or 3 compared to genotype 1. Adverse effects were primarily flu-like symptoms and neutropenia. There were insufficient data to assess the applicability of the week 12 stop rule (stopping therapy at week 12 if there is less than a 2 log drop in HCV RNA) or the efficacy of shortening therapy to 24 weeks in children with genotype 2 and 3.

CONCLUSIONS/SIGNIFICANCE: Current guidelines for the treatment of HCV in children are based on limited data. Further research is needed to define the optimal therapy for HCV in children.

摘要

背景

目前的指南建议采用与成人相同的原则对丙型肝炎病毒(HCV)感染的儿童进行治疗。然而,很少有研究评估 HCV 治疗在儿童中的疗效和安全性。

方法/主要发现:对评估 HCV 治疗在儿童中的疗效和安全性的研究进行了系统文献回顾。主要结局是持续病毒学应答(SVR),并对基因型的应答率进行了亚组分析。有 4 项随机对照试验(RCT)和 31 项非随机研究,均涉及干扰素、聚乙二醇干扰素(PEG-IFN)或这些药物与利巴韦林的联合应用。由于研究人群和干预措施不同,无法直接比较 SVR 率。基因型未报告或与研究之间存在显著差异。PEG-IFN 和利巴韦林的总体 SVR 率为 30%至 100%,与成人的 SVR 率相当。与成人相似,基因型 2 或 3 的儿童 SVR 率明显高于基因型 1。不良反应主要是流感样症状和中性粒细胞减少症。数据不足,无法评估第 12 周停药规则(如果 HCV RNA 下降小于 2 个对数,则在第 12 周停止治疗)或在基因型 2 和 3 的儿童中将治疗缩短至 24 周的疗效。

结论/意义:目前儿童 HCV 治疗的指南是基于有限的数据。需要进一步研究来确定 HCV 治疗在儿童中的最佳治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6154/2903479/9443913d5940/pone.0011542.g001.jpg

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