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Discussion on critical points for a tailored therapy to cure hepatitis C virus infection
Article in English | WPRIM (Western Pacific) | ID: wpr-763381
Responsible library: WPRO
ABSTRACT
Hepatitis C virus (HCV) infects around 71 million people worldwide and in 2018 it is still a major health problem. Since 2011, anti-HCV therapy with availability of direct-acting antiviral drugs has revolutionized the clinical response and paved the way to eradication strategies. However, despite the high rate of sustained virological response, treatment failure may occur in a limited percentage of patients, possibly due to resistance-associated substitutions (RASs), either emergent or pre-existent even in minority viral populations. Clearly this problem may impair success of eradication strategies. With this background, several questions marks still exist around HCV treatment, including whether pan-genotypic treatments with complete effectiveness in any clinical conditions really exist outside clinical trials, the actual cost-effectiveness of genotyping testing, and utility of RAS detection in viral quasispecies by next generation sequencing approach. In this review, we describe these critical points by discussing recent literature data and our research experience.
Subject(s)

Full text: Available Health context: SDG3 - Health and Well-Being Health problem: Target 3.3: End transmission of communicable diseases Database: WPRIM (Western Pacific) Main subject: Antiviral Agents / Genetic Variation / Hepatitis C / Treatment Failure / Hepacivirus / High-Throughput Nucleotide Sequencing / Hepatitis Limits: Humans Language: English Journal: Clinical and Molecular Hepatology Year: 2019 Document type: Article
Full text: Available Health context: SDG3 - Health and Well-Being Health problem: Target 3.3: End transmission of communicable diseases Database: WPRIM (Western Pacific) Main subject: Antiviral Agents / Genetic Variation / Hepatitis C / Treatment Failure / Hepacivirus / High-Throughput Nucleotide Sequencing / Hepatitis Limits: Humans Language: English Journal: Clinical and Molecular Hepatology Year: 2019 Document type: Article
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