Drug resistance profile and clinical features for hepatitis C patients experiencing DAA failure in Taiwan

Chun Ming Hong, You Yu Lin, Chun Jen Liu, Ya Yun Lai, Shiou Hwei Yeh, Hung Chih Yang, Jia Horng Kao, Shih Jer Hsu, Yi Hsiang Huang, Sheng Shun Yang, Hsing Tao Kuo, Pin Nan Cheng, Ming Lung Yu*, Pei Jer Chen

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

8 Scopus citations

Abstract

About 4% of the population in Taiwan are seropositive for anti-HCV Ab and 70% with HCV RNA. To address this high chronic hepatitis C disease load, Taiwan National Health Insurance started reimbursing genotype-specific DAAs in 2017 and pangenotype DAAs in mid-2018. With a 97% SVR12 rate, there were still 2–3% of patients that failed to clear HCV. To understand the causes of DAA failure in Taiwan, we conducted a multi-center, clinical, and virologic study. A total of 147 DAA-failure patients were recruited, and we searched HCV NS3/4A, NS5A and NS5B for known resistance-associated substitutions (RASs) by population sequencing, and conducted whole genome sequencing (WGS) for those without known RASs. A total of 107 patients received genotype-specific DAAs while 40 had pangenotype DAAs. Clinically, the important cause of failure is poor adherence. Virologically, common RASs in genotype-specific DAAs were NS5A-L31, NS5A-Y93, and NS5B-C316, while common RASs in pangenotype DAAs were NS5A-L31, NS5A-A/Q/R30, and NS5A-Y93. Additionally, new amino acid changes were found by WGS. Finally, we identified 12 cases with inconsistent baseline and post-treatment HCV genotypes, which is suggestive of re-infection rather than treatment failure. Our study described the drug resistance profile for DAA failure in Taiwan, showing differences from other countries.

Original languageEnglish
Article number2294
JournalViruses
Volume13
Issue number11
DOIs
StatePublished - Nov 2021

Keywords

  • Chronic hepatitis C
  • Direct-acting antiviral agent
  • Resistance-associated substitution
  • Taiwan
  • Treatment failure
  • Whole genome sequencing

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