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1.
Clinical and Molecular Hepatology ; : 30-36, 2019.
Article in English | WPRIM | ID: wpr-763381

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)
Humans , Antiviral Agents , Genetic Variation , Hepacivirus , Hepatitis C , Hepatitis , High-Throughput Nucleotide Sequencing , Treatment Failure
2.
Clinical and Molecular Hepatology ; : 278-293, 2018.
Article in English | WPRIM | ID: wpr-716620

ABSTRACT

The paradigm for the treatment of chronic hepatitis C (CHC) has been changed due to the development of direct acting antivirals (DAAs) of hepatitis C virus (HCV). The high sustained virologic response rate and ease of administration makes the DAAs approach ideal to contribute to the complete eradication of HCV. Currently, treatment options for individual patients vary depending on the genotype or subtype of HCV, presence or absence of liver cirrhosis, previous experience of antiviral treatment or resistance associated substitutions. Because of drug avalilability, cost-effectiveness, preference, compliance and greater possibility of desirable effects and presumed patient-important outcomes may vary between countries, treatment options for individual patients are different. The review focuses on the comparing the current treatment options for CHC in other continents with the 2017 Korea Association for the Study of the Liver guidelines.


Subject(s)
Humans , Antiviral Agents , Compliance , Genotype , Hepacivirus , Hepatitis C, Chronic , Hepatitis, Chronic , Korea , Liver Cirrhosis , Liver
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