Literature DB >> 27059129

Survival of patients with HCV cirrhosis and sustained virologic response is similar to the general population.

Savino Bruno1, Vito Di Marco2, Massimo Iavarone3, Luigi Roffi4, Andrea Crosignani5, Vincenza Calvaruso2, Alessio Aghemo3, Giuseppe Cabibbo2, Mauro Viganò3, Vincenzo Boccaccio6, Antonio Craxí2, Massimo Colombo3, Patrick Maisonneuve7.   

Abstract

BACKGROUND & AIMS: Life expectancy of patients with compensated hepatitis C virus (HCV) cirrhosis achieving sustained virologic response (SVR) is limited by liver events as compared to the general population. Thus, survival benefit of SVR remains to be measured.
METHODS: The study includes prospective surveillance data from three cohorts of Italian patients with compensated HCV cirrhosis who achieved SVR on an interferon-based (IFN) regimen, compared to simultaneously observed non-SVR, untreated and decompensated patients. Overall survival was calculated from the date of start of IFN to death. The number of deaths expected during the at-risk period was determined by applying age- and sex-specific mortality rates recorded in Italy for person-years adequate for the enrolment period. The standardized mortality ratio (SMR) determined the relative risk of death over that of the age and sex matched general population.
RESULTS: Overall, 28/181 patients followed-up for a median period of 9.6years (range 1-25years) died. The 10 and 20-year overall survival rates for the whole series were 90.9% (95% CI, 84.3-94.8) and 62.9% (95% CI, 45.9-75.9), respectively. The number of expected deaths in the corresponding age and sex matched general population was 28.1, corresponding to a SMR=1.00 (95% CI, 0.72-1.35), with an SMR for non-SVR patients of 3.85 (95% CI, 3.43-4.30), for untreated of 3.01 (95% CI, 2.64-3.42) and for decompensated of 6.70 (95% CI, 5.39-8.22).
CONCLUSIONS: Patients with compensated HCV cirrhosis achieving SVR by IFN obtain a main benefit levelling their survival curve to that of the general population. Wider applicability of IFN-free regimens will possibly make this achievement more generalizable.
Copyright © 2016 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Antiviral therapy; DAA’s; HCV-related cirrhosis; IFN-based therapy; SVR

Mesh:

Substances:

Year:  2016        PMID: 27059129     DOI: 10.1016/j.jhep.2016.01.034

Source DB:  PubMed          Journal:  J Hepatol        ISSN: 0168-8278            Impact factor:   25.083


  27 in total

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8.  Impact of hepatitis C virus core mutations on the response to interferon-based treatment in chronic hepatitis C.

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9.  Long-term follow-up of clinical trial patients treated for chronic HCV infection with daclatasvir-based regimens.

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Journal:  Liver Int       Date:  2017-10-12       Impact factor: 5.828

Review 10.  Hepatitis C-related hepatocellular carcinoma in the era of new generation antivirals.

Authors:  Thomas F Baumert; Frank Jühling; Atsushi Ono; Yujin Hoshida
Journal:  BMC Med       Date:  2017-03-14       Impact factor: 11.150

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