Ledipasvir/sofosbuvir combination for chronic hepatitis C infection in children and adolescents

被引:7
作者
Quintero, Jesus [1 ]
Juamperez, Javier [1 ]
Julio, Ecaterina [1 ]
Cabello, Vanessa [2 ]
Mercadal-Hally, Maria [1 ]
Soler-Palacin, Pere [3 ]
Segarra, Oscar [2 ]
Rodrigo, Carlos [4 ]
机构
[1] Univ Autonoma Barcelona, Hosp Univ Vall dHebron, Unidad Hepatol & Trasplante Hepat Pediat, Barcelona, Spain
[2] Hosp Univ Vall dHebron, Unidad Gastroenterol Hepatol & Nutr Pediat, Barcelona, Spain
[3] Hosp Univ Vall dHebron, Unidad Enfermedades Infecciosas Pediat, Barcelona, Spain
[4] Univ Atonoma Barcelona, Hosp Univ Vall dHebron, Serv Pediat, Barcelona, Spain
来源
ANALES DE PEDIATRIA | 2019年 / 90卷 / 03期
关键词
Chronic hepatitis C infection; Direct-acting antivirals; Sustained viral response; VIRUS-INFECTION; CHRONIC HCV; SOFOSBUVIR; LEDIPASVIR; RIBAVIRIN; EFFICACY; TRANSMISSION; SAFETY;
D O I
10.1016/j.anpedi.2018.07.007
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
INTRODUCTION: Hepatitis C virus infection is world health problem. The aim of this study was to assess the safety and efficacy of ledipasvir/sofosbuvir combination in chronic Hepatitis C Virus (HCV) genotype 1 and 4 infection in paediatric patients. METHODS: Eligible patients to be treated with ledipasvir/sofosbuvir were patients from 6 to 18 years old with a chronic HCV genotype 1 or 4 infection. The duration and doses of antiviral drugs were changed depending on patient age, fibrosis stage, and PEGylated interferon+ribavirin experience status. The primary efficacy endpoint was the percentage of patients with a sustained virological response 12 weeks post-treatment. RESULTS: A total of nine patients (7 males) with a median age of 14.8 years (8.48-17.91) were treated with ledipasvir/sofosbuvir combination. Five patients received previous treatment with PEGylated interferon+ribavirin during a median of 8.5 months (3-12 months). Eight patients had some degree of fibrosis (1 patient presented with F1, three patients F2, 2 patients F3, and 2 patients F4). The median pre-treatment viral load was 6.2 Log [5.9-6.8] with the HCV RNA becoming negative six weeks after starting the treatment in 100% of the patients. All patients maintained a sustained viral response at 12 weeks. Three patients (33.3%) had some type of adverse effect (2 headache and one oral thrush). The median post-treatment follow-up was 24 weeks (12-104). CONCLUSIONS: Treatment with ledipasvir/sofosbuvir in paediatric patients with chronic HCV infection genotype 1 and 4 is safe and effective with SVR12 and similar to those reported in adults. Copyright (c) 2018. Publicado por Elsevier Espana, S.L.U.Published by Elsevier Espana, S.L.U. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/ticenses/by-nc-nd/1.0/).
引用
收藏
页码:141 / 147
页数:7
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