Suboptimal SVR rates in African patients with atypical genotype 1 subtypes: Implications for global elimination of hepatitis C

被引:63
作者
Childs, Kate [1 ]
Davis, Christopher [2 ]
Cannon, Mary [1 ]
Montague, Sarah [1 ]
Filipe, Ana [2 ]
Tong, Lily [2 ]
Simmonds, Peter [3 ]
Smith, Donald [3 ,4 ]
Thomson, Emma C. [2 ]
Dusheiko, Geoff [1 ]
Agarwal, Kosh [1 ]
机构
[1] Kings Coll Hosp Trust, Inst Liver Studies, London, England
[2] Univ Glasgow, Ctr Virus Res, MRC, Glasgow, Lanark, Scotland
[3] Univ Oxford, Nuffield Dept Med, Oxford, England
[4] Univ Edinburgh, ICTV Online Report 10, Edinburgh, Midlothian, Scotland
基金
英国医学研究理事会; 英国惠康基金;
关键词
Hepatitis C; Antiviral Therapy; Africa; Treatment Failures; RESISTANCE-ASSOCIATED SUBSTITUTIONS; EARLY ACCESS PROGRAM; RARE HCV SUBTYPES; DAA THERAPY; VIRUS; PREVALENCE; LEDIPASVIR; NS5A;
D O I
10.1016/j.jhep.2019.07.025
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background & Aims: HCV subtypes which are unusual in Europe are more prevalent in the African region, but little is known of their response to direct-acting antivirals (DAAs). These include non-1a/1b/ non-subtypeable genotype 1 (G1) or non-4a/4d (G4). In this report we aimed to describe the genotype distribution and treatment outcome in a south London cohort of African patients. Methods: We identified all patients born in Africa who attended our clinic from 2010-2018. Information on HCV genotype, treatment regimen and outcome were obtained. Non-subtypeable samples were analysed using Glasgow NimbleGen next-generation sequencing (NGS). Phylogenetic analysis was carried out by generating an uncorrected nucleotide p-distance tree from the complete coding regions of our sequences. Results: Of 91 African patients, 47 (52%) were infected with an unusual subtype. Fourteen novel, as yet undesignated subtypes (G1*), were identified by NGS. Three individuals were infected with the same subtype, now designated as subtype 1p. Baseline sequences were available for 22 patients; 18/22 (82%) had baseline NS5A resistance-associated substitutions (RASs). Sustained virological response (SVR) was achieved in 56/63 (89%) overall, yet only in 21/28 (75%) of those with unusual G1 subtypes, with failure in 3/16 G1*, 1/2 G1p and 3/3 in G1l. Six treatment failures occurred with sofosbuvir/ledipasvir compared to 1 failure on a PI-based regimen. The SVR rate for all other genotypes and subtypes was 35/35 (100%). Conclusions: Most individuals in an unselected cohort of African patients were infected with an unusual genotype, including novel subtype 1p. The SVR rate of those with unusual G1 subtypes was 75%, raising concern about expansion of DAAs across Africa. Depending on the regimen used, higher failure rates in African cohorts could jeopardise HCV elimination. Lay summary: Direct-acting antiviral medications are able to cure hepatitis C in the majority of patients. The most common genotype of hepatitis C in Europe and the United States is genotype la or 1b and most clinical trials focused on these geno-types. We report that in a group of African patients, most of them had unusual (non-1a/1b) genotype 1 subtypes, and that the cure rate in these unusual genotypes was lower than in genotypes la and 1b. (C) 2019 European Association for the Study of the Liver. Published by Elsevier B.V.
引用
收藏
页码:1099 / 1105
页数:7
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