Background Liver disease progression after Hepatitis C Virus (HCV) eradication following direct-acting antiviral (DAA) treatment in the real-life setting according to Human Immunodefciency Virus (HIV) coinfection was evaluated. Methods Patients consecutively enrolled in PITER between April 2014 and June 2019 and with at least 12-weeks follow-up following treatment were analysed. Cox regression analysis were used to evaluate HIV coinfection and factors independently associated with liver disease outcomes following viral eradication in DAA treated patients with pre-treatment liver cirrhosis. Results 93 HIV/HCV coinfected and 1109 HCV monoinfected patients were evaluated during a median follow-up of 26.7 (range 6–44.6) and 24.6 (range 6.8–47.3) months, respectively. No diference in the cumulative HCC incidence and hepatic decompensation was observed between coinfected and monoinfected patients. Age (Hazard Ratio [HR]=1.08; 95% CI 1.04–1.13), male sex (HR=2.76; 95% CI 1.28–5.96), lower albumin levels (HR=3.94; 95% CI 1.81–8.58), genotype 3 (HR=5.05; 95% CI 1.75–14.57) and serum anti-HBc positivity (HR=1.99, 95% CI 1.01–3.95) were independently associated with HCC incidence. Older age (HR=1.03; 95% CI 1.00–1.07), male sex (HR=2.13; 95% CI 1.06–4.26) and lower albumin levels (HR=3.75; 95% CI 1.89–7.46) were independently associated with the appearance of a decompensating event after viral eradication. Conclusion Diferent demographic, clinical and genotype distribution between HIV coinfected vs those monoinfected, was observed in a representative cohort of HCV infected patients in Italy. Once liver cirrhosis is established the disease progression is decreased, but still persists regardless of viral eradication in both coinfected and monoinfected patients. In patients with cirrhosis, HIV coinfection was not associated with a higher probability of liver complications, after viral eradication.

Advanced liver disease outcomes after hepatitis C eradication by human immunodeficiency virus infection in PITER cohort

Maria Vinci;Luchino Chessa
Membro del Collaboration Group
;
2020-01-01

Abstract

Background Liver disease progression after Hepatitis C Virus (HCV) eradication following direct-acting antiviral (DAA) treatment in the real-life setting according to Human Immunodefciency Virus (HIV) coinfection was evaluated. Methods Patients consecutively enrolled in PITER between April 2014 and June 2019 and with at least 12-weeks follow-up following treatment were analysed. Cox regression analysis were used to evaluate HIV coinfection and factors independently associated with liver disease outcomes following viral eradication in DAA treated patients with pre-treatment liver cirrhosis. Results 93 HIV/HCV coinfected and 1109 HCV monoinfected patients were evaluated during a median follow-up of 26.7 (range 6–44.6) and 24.6 (range 6.8–47.3) months, respectively. No diference in the cumulative HCC incidence and hepatic decompensation was observed between coinfected and monoinfected patients. Age (Hazard Ratio [HR]=1.08; 95% CI 1.04–1.13), male sex (HR=2.76; 95% CI 1.28–5.96), lower albumin levels (HR=3.94; 95% CI 1.81–8.58), genotype 3 (HR=5.05; 95% CI 1.75–14.57) and serum anti-HBc positivity (HR=1.99, 95% CI 1.01–3.95) were independently associated with HCC incidence. Older age (HR=1.03; 95% CI 1.00–1.07), male sex (HR=2.13; 95% CI 1.06–4.26) and lower albumin levels (HR=3.75; 95% CI 1.89–7.46) were independently associated with the appearance of a decompensating event after viral eradication. Conclusion Diferent demographic, clinical and genotype distribution between HIV coinfected vs those monoinfected, was observed in a representative cohort of HCV infected patients in Italy. Once liver cirrhosis is established the disease progression is decreased, but still persists regardless of viral eradication in both coinfected and monoinfected patients. In patients with cirrhosis, HIV coinfection was not associated with a higher probability of liver complications, after viral eradication.
2020
Hepatitis C virus; Human immunodeficiency virus; Coinfection; Real-life cohort; Direct-acting antivirals; Advanced liver disease; Sustained virological response; Clinical outcomes; Cirrhosis; Hepatocellular carcinoma; Viral eradication
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11584/290450
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