Theme: Clinical Research Year: 2019
Background: Two years after cure with LDV/SOF (09/2015-03/2016, SVR12 06/2016), a 56-year-old
patient with history of IVDU and compensated cirrhosis due to chronic hepatitis C (genotype 1b)
diagnosed in 2013 presented with viral resurgence (HCV RNA 1.5 x 105
IU/ml). Undetectable HCV RNA
loads < 12 IU/ml had been documented on three distinct occasions in the meantime (09/2016, 05/2017 and 02/2018). The patient under stable opioid-substitution without IV drug-use for >15 years and
excellent adherence to previous therapy did not show any risk behavior for reinfection.
Methods: NS3, NS5A and NS5B sequences from plasma samples collected prior to treatment and
following relapse were amplified with PCR and sequenced by next-generation sequencing. Consensus
sequences of each time-point were compared to determine the percentage of homology and
appearance of resistance-associated substitutions(RAS). The sequences were compared to the genetic
database of the French National Reference Center for Hepatitis. Extensive inquiries about possible
reinfection were carried out.
Results: NS5B sequences from 2015 and 2018 showed a sequence homology of 99.6%,suggesting viral
relapse. A Y93H RAS in NS5A appeared in 2018, present in 99.5% of the viral population, but was not
detectable in 2015 prior to treatment (minority cut-off 1%). Phylogenetic analysis of the NS5B region
demonstrated a 99% bootstrap value between the samples supporting HCV relapse. No source of
reinfection with the same virus could be identified.
Conclusion: We show HCV relapse with a Y93H RAS selected by the previous treatment with LDV/SOF.
The published incidence of late relapse after SOF-containing DAA-based therapy is very low (<0.5%). The majority of relapse occurred before 24 weeks post-treatment, making this case with >90 weeks
post-treatment even more exceptional. Genetic analyses investigating viral resurgence should be
encouraged. Treatment with GLE/PIB plus SOF plus RBV for a duration of 6 months was started in