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Rare HCV subtypes and retreatment outcomes in a cohort of European DAA-experienced patients.
Dietz, Julia; Graf, Christiana; Berg, Christoph P; Port, Kerstin; Deterding, Katja; Buggisch, Peter; Peiffer, Kai-Henrik; Vermehren, Johannes; Dultz, Georg; Geier, Andreas; Reiter, Florian P; Bruns, Tony; Schattenberg, Jörn M; Durmashkina, Elena; Gustot, Thierry; Moreno, Christophe; Trauth, Janina; Discher, Thomas; Fischer, Janett; Berg, Thomas; Kremer, Andreas E; Müllhaupt, Beat; Zeuzem, Stefan; Sarrazin, Christoph.
Afiliação
  • Dietz J; Medical Clinic 1, Department of Medicine, Goethe University, Frankfurt, Germany.
  • Graf C; German Center for Infection Research (DZIF), External Partner Site Frankfurt, Germany.
  • Berg CP; Medical Clinic 1, Department of Medicine, Goethe University, Frankfurt, Germany.
  • Port K; German Center for Infection Research (DZIF), External Partner Site Frankfurt, Germany.
  • Deterding K; Department of Internal Medicine II, University Hospital Munich, Munich, Germany.
  • Buggisch P; Department of Internal Medicine I, University of Tübingen, Tübingen, Germany.
  • Peiffer KH; Department of Gastroenterology, Hepatology and Endocrinology, Medizinische Hochschule Hannover, Hannover, Germany.
  • Vermehren J; Department of Gastroenterology, Hepatology and Endocrinology, Medizinische Hochschule Hannover, Hannover, Germany.
  • Dultz G; Institute for Interdisciplinary Medicine IFI, Hamburg, Germany.
  • Geier A; Medical Clinic 1, Department of Medicine, Goethe University, Frankfurt, Germany.
  • Reiter FP; Department of Internal Medicine B, University of Münster, Münster, Germany.
  • Bruns T; Medical Clinic 1, Department of Medicine, Goethe University, Frankfurt, Germany.
  • Schattenberg JM; Medical Clinic 1, Department of Medicine, Goethe University, Frankfurt, Germany.
  • Durmashkina E; Division of Hepatology, Department of Medicine II, University Hospital Würzburg, Würzburg, Germany.
  • Gustot T; Division of Hepatology, Department of Medicine II, University Hospital Würzburg, Würzburg, Germany.
  • Moreno C; Department of Medicine III, University Hospital Aachen, Aachen, Germany.
  • Trauth J; Department of Internal Medicine II, Saarland University Medical Center Homburg, Homburg, Germany.
  • Discher T; Saarland University, Saarbrücken, Germany.
  • Fischer J; Medizinische Klinik 2, St. Josefs-Hospital, Wiesbaden, Germany.
  • Berg T; Department of Gastroenterology, Hepatopancreatology and Digestive Oncology, CUB Hôpital Erasme, Université Libre de Bruxelles, Brussels, Belgium.
  • Kremer AE; Department of Gastroenterology, Hepatopancreatology and Digestive Oncology, CUB Hôpital Erasme, Université Libre de Bruxelles, Brussels, Belgium.
  • Müllhaupt B; Department of Internal Medicine II, Section of Infectious Diseases, Justus-Liebig-University Giessen, Giessen, Germany.
  • Zeuzem S; German Lung Center (DZL), Giessen, Germany.
  • Sarrazin C; Department of Internal Medicine II, Section of Infectious Diseases, Justus-Liebig-University Giessen, Giessen, Germany.
JHEP Rep ; 6(7): 101072, 2024 Jul.
Article em En | MEDLINE | ID: mdl-39006503
ABSTRACT
Background and

Aims:

Data on the prevalence and characteristics of so-called rare HCV genotypes (GTs) in larger cohorts is limited. This study investigates the frequency of rare GT and resistance-associated substitutions and the efficacy of retreatment in a European cohort.

Methods:

A total of 129 patients with rare GT1-6 were included from the European resistance database. NS3, NS5A, and NS5B were sequenced and clinical parameters and retreatment efficacies were collected retrospectively.

Results:

Overall 1.5% (69/4,656) of direct-acting antiviral (DAA)-naive and 4.4% (60/1,376) of DAA-failure patients were infected with rare GT. Although rare GTs were almost equally distributed throughout GT1-6 in DAA-naive patients, we detected mainly rare GT4 (47%, 28/60 GT4; of these n = 17, subtype 4r) and GT3 (25%, 15/60 GT3, of these n = 8, subtype 3b) among DAA-failures. A total of 62% (37/60) of DAA failures had not responded to first-generation regimes and the majority was infected with rare GT4 (57%, 21/37). In contrast, among patients with failure to pangenotypic DAA regimens (38%, 23/60), infections with rare GT3 were overrepresented (57%, 13/23). Although NS5A RASs were uncommon in rare GT2, GT5a, and GT6, we observed combined RASs in rare GT1, GT3, and GT4 at positions 28, 30, 31, which can be considered as inherent. DAA failures with completed follow-up of retreatment, achieved a high SVR rate (94%, 45/48 modified intention-to-treat analysis; 92%, 45/49 intention-to-treat). Three patients with GT4f, 4r, or 3b, respectively, had virological treatment failure.

Conclusions:

In this European cohort, rare HCV GT were uncommon. Accumulation of specific rare GT in DAA-failure patients suggests reduced antiviral activities of DAA regimens. The limited global availability of pangenotypic regimens for first line therapy as well as multiple targeted regimens for retreatment could result in HCV elimination targets being delayed. Impact and implications Data on the prevalence and characteristics of rare HCV genotypes (GT) in larger cohorts are still scarce. This study found low rates of rare HCV GTs among European HCV-infected patients. In direct-acting antiviral (DAA)-failure patients, rare GT3 subtypes accumulated after pangenotypic DAA treatment and rare GT4 after first generation DAA failure and viral resistance was detected at NS5A positions 28, 30, and 31. The limited global availability of pangenotypic DAA regimens for first line therapy as well as multiple targeted regimens for retreatment could result in HCV elimination targets being delayed.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article