索非布韦和维帕他韦联合疗法治疗儿童和青少年慢性丙型肝炎的概况:当前证据

IF 2.8 3区 医学 Q1 Pharmacology, Toxicology and Pharmaceutics Therapeutics and Clinical Risk Management Pub Date : 2024-01-11 DOI:10.2147/tcrm.s326099
Dania Brigham, Michael R Narkewicz
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引用次数: 0

摘要

摘要:慢性丙型肝炎(HCV)影响着多达 325 万儿童和青少年。早期治疗儿童和青少年的丙型肝炎病毒可减少发展为晚期肝病和癌症的几率。丙型肝炎病毒(HCV)的治疗已发展为成人高效直接作用抗病毒疗法,现在也适用于≥3 岁的儿童。本综述重点介绍索非布韦和维帕他韦(SOF/VEL)的作用,这是一种治疗儿童和青少年慢性丙型肝炎病毒的新疗法。SOF/VEL 是一种泛基因型 DAA,主要通过肝脏和胆汁排泄清除。该药物已在儿童和青少年中进行过研究,并在美国获准用于年龄≥ 3 岁的儿童和青少年。尽管目前数据有限,但 SOF/VEL 的持续病毒应答率与同类 DAAs 相似,在 95%-98% 之间。迄今为止,副作用极小。 关键词:小儿丙型肝炎、小儿丙型肝炎治疗
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Profile of Sofosbuvir and Velpatasvir Combination in the Treatment of Chronic Hepatitis C in Children and Adolescents: Current Evidence
Abstract: Chronic hepatitis C (HCV) affects up to 3.25 million children and adolescents. Early treatment of HCV in children and adolescents reduces progression to advanced liver disease and cancer. Treatment for HCV has evolved to highly effective direct acting antiviral therapy in adults and now in children ≥ 3 years of age. This review focuses on the role of sofosbuvir and velpatasvir (SOF/VEL), a newer treatment of children and adolescents with chronic HCV. SOF/VEL is a pangenotypic DAA with primary clearance via the liver and biliary excretion. It has been studied in children and adolescents and is approved in the US for use in children and adolescents ≥ 3 years of age. Although the data are currently limited, SOF/VEL has demonstrated sustained viral response rates similar to comparable DAAs in the range of 95– 98%. To date, side effects have been minimal.

Keywords: pediatric hepatitis C, pediatric hepatitis C treatment
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来源期刊
Therapeutics and Clinical Risk Management
Therapeutics and Clinical Risk Management HEALTH CARE SCIENCES & SERVICES-
CiteScore
5.30
自引率
3.60%
发文量
139
审稿时长
16 weeks
期刊介绍: Therapeutics and Clinical Risk Management is an international, peer-reviewed journal of clinical therapeutics and risk management, focusing on concise rapid reporting of clinical studies in all therapeutic areas, outcomes, safety, and programs for the effective, safe, and sustained use of medicines, therapeutic and surgical interventions in all clinical areas. The journal welcomes submissions covering original research, clinical and epidemiological studies, reviews, guidelines, expert opinion and commentary. The journal will consider case reports but only if they make a valuable and original contribution to the literature. As of 18th March 2019, Therapeutics and Clinical Risk Management will no longer consider meta-analyses for publication. The journal does not accept study protocols, animal-based or cell line-based studies.
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