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Follow‐up of sustained virological responders with hepatitis C and advanced liver disease after interferon/ribavirin‐free treatment
Author(s) -
Kozbial Karin,
Moser Stephan,
AlZoairy Ramona,
Schwarzer Remy,
Datz Christian,
Stauber Rudolf,
Laferl Hermann,
Strasser Michael,
Beinhardt Sandra,
Stättermayer Albert F.,
Gschwantler Michael,
Zoller Heinz,
Maieron Andreas,
Graziadei Ivo,
Trauner Michael,
SteindlMunda Petra,
Hofer Harald,
Ferenci Peter
Publication year - 2018
Publication title -
liver international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.873
H-Index - 110
eISSN - 1478-3231
pISSN - 1478-3223
DOI - 10.1111/liv.13629
Subject(s) - medicine , ribavirin , hepatocellular carcinoma , cirrhosis , gastroenterology , decompensation , hepatitis c , liver transplantation , liver disease , transplantation , hepatitis c virus , immunology , virus
Background The introduction of direct‐acting antivirals ( DAA ) has increased sustained virological response ( SVR ) rates in patients with advanced liver disease and chronic hepatitis C( CHC )infection. At present, data on clinical outcome and long‐term durability of viral eradication after successful DAA therapy are scarce. Aim To evaluate the long‐term success of viral eradication in patients with advanced fibrosis or cirrhosis treated with DAA s. Methods Five hundred and fifty‐one patients with advanced fibrosis (n = 158) or cirrhosis ( CPS ‐A:317, CPS ‐B/C:76) and SVR after interferon and ribavirin‐free DAA therapy treated between October 2013 and April 2016 were studied with a median follow‐up of 65.6 (13.0‐155.3) weeks. Only patients without hepatocellular carcinoma ( HCC ) at baseline and without liver transplantation were included. Results Twelve patients (2.2%) died during follow‐up: the mortality rate was 0.6% in F3, 2.2% in CPS ‐A and 5.3% in CPS ‐B/C patients ( P = .08). During follow‐up 36 patients with cirrhosis (9.1%) developed a liver related event, including 16 with de‐novo HCC (4.1%). Seven patients were transplanted at a median of 9.7 (range 3.8‐21.7) months after EOT . History of decompensation was significantly associated with liver related events during follow‐up ( HR 7.9; 95% CI 2.7‐22.6; P < .001), and with mortality ( HR 5.5; 95% CI 1.5‐20.2, P = .01). Conclusions Eradication of HCV by DAA therapy was durable irrespective of the DAA combination used. Most of the cured patients had an excellent long‐term clinical prognosis. Nevertheless, the risk of new occurrence of HCC remains worrisome and thus regular surveillance is obligatory even after clinical stabilization and improvement of the patient.