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Optimal efficacy of interferon-free HCV retreatment after protease inhibitor failure in real life

Articolo
Data di Pubblicazione:
2017
Abstract:
OBJECTIVES:

First-generation protease-inhibitors (PIs) have suboptimal efficacy in GT-1 patients with advanced liver disease, and patients experiencing treatment failure may require urgent retreatment. Our objective was to analyse the real-life efficacy of interferon (IFN)-free retreatment after PI-failure, and the role of genotypic-resistance-testing (GRT) in guiding retreatment choice.
METHODS:

In this multi-centre observational study, patients retreated with IFN-free regimens after first-generation PI-failure (telaprevir-boceprevir-simeprevir) were included. Sustained-virological-response (SVR) was evaluated at week 12 of follow-up. GRT was performed by population-sequencing.
RESULTS:

After PI-failure, 121 patients (cirrhotic=86.8%) were retreated following three different strategies: A) with 'GRT-guided' regimens (N=18); B) with 'AASLD/EASL recommended, not GRT-guided' regimens (N=72); C) with 'not recommended, not GRT-guided' regimens (N=31). Overall SVR rate was 91%, but all 18 patients treated with 'GRT-guided' regimens reached SVR (100%), despite heterogeneity in treatment duration, use of PI and ribavirin, versus 68/72 patients (94.4%) receiving 'AASLD/EASL recommended, not GRT-guided' regimens. SVR was strongly reduced (77.4%) among the 31 patients who received a 'not recommended, not GRT-guided regimen' (p <0.01). Among 37 patients retreated with a PI, SVR rate was 89.2% (33/37). Four GT-1a cirrhotic patients failed an option (C) simeprevir-containing treatment; three out of four had a baseline R155K NS3-RAS. All seven patients treated with paritaprevir-containing regimens reached SVR, regardless of treatment duration and performance of a baseline-GRT.
CONCLUSION:

Retreatment of PI-experienced patients can induce maximal SVR rates in real life. Baseline-GRT could help to optimize retreatment strategy, allowing PIs to be reconsidered when chosen after a RASs evaluation.
Tipologia CRIS:
1.1 Articolo in rivista
Keywords:
Cirrhosis; Direct acting antivirals; Genotypic resistance testing; HCV failure; HCV resistance; NS5A-inhibitors; Protease-inhibitors; Retreatment; Microbiology (medical); Infectious Diseases
Elenco autori:
Cento, V.; Barbaliscia, S.; Lenci, I.; Ruggiero, T.; Magni, C. F.; Paolucci, S.; Babudieri, S.; Siciliano, MANUELE KOCI; Pasquazzi, C.; Ciancio, A.; Perno, C. F.; Ceccherini-Silberstein, F.; Micheli, V.; Troshina, Y.; Biliotti, E.; Milana, M.; Melis, M.; Teti, E.; Lambiase, L.; Menzaghi, B.; Nicolini, L. A.; Marenco, S.; Di Maio, V. C.; Aragri, M.; Pecchioli, A.; Bertoli, A.; Sarrecchia, C.; Macera, M.; Coppola, N.; Puoti, M.; Romagnoli, D.; Pellicelli, A.; Bonora, S.; Novati, S.; Baldanti, F.; Ghisetti, V.; Andreoni, M.; Taliani, G.; Rizzardini, G.; Angelico, M.
Autori di Ateneo:
BALDANTI FAUSTO
Link alla scheda completa:
https://iris.unipv.it/handle/11571/1211262
Pubblicato in:
CLINICAL MICROBIOLOGY AND INFECTION
Journal
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URL

http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1469-0691
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