Division of Hospital Medicine, Department of Internal Medicine, National Taiwan University Hospital, Taipei 10022, Taiwan.
Graduate Institute of Clinical Medicine, National Taiwan University College of Medicine, Taipei 10002, Taiwan.
Viruses. 2021 Nov 17;13(11):2294. doi: 10.3390/v13112294.
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.
台湾约有 4%的人口抗 HCV Ab 呈阳性,70%的人 HCV RNA 呈阳性。为了解决这一高慢性丙型肝炎疾病负担,台湾全民健康保险于 2017 年开始报销基因型特异性 DAA,并于 2018 年年中报销泛基因型 DAA。尽管 SVR12 率达到 97%,仍有 2-3%的患者未能清除 HCV。为了了解台湾 DAA 失败的原因,我们进行了一项多中心的临床和病毒学研究。共招募了 147 例 DAA 失败患者,我们通过群体测序对 HCV NS3/4A、NS5A 和 NS5B 进行了已知耐药相关取代(RAS)的检测,并对那些没有已知 RAS 的患者进行了全基因组测序(WGS)。共有 107 例患者接受了基因型特异性 DAA,40 例患者接受了泛基因型 DAA。临床方面,失败的重要原因是依从性差。病毒学方面,基因型特异性 DAA 的常见 RAS 为 NS5A-L31、NS5A-Y93 和 NS5B-C316,而泛基因型 DAA 的常见 RAS 为 NS5A-L31、NS5A-A/Q/R30 和 NS5A-Y93。此外,还通过 WGS 发现了新的氨基酸变化。最后,我们鉴定了 12 例基线和治疗后 HCV 基因型不一致的病例,提示可能是再感染而不是治疗失败。我们的研究描述了台湾 DAA 失败的耐药谱,与其他国家有所不同。