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Effect of direct-acting antivirals on future occurrence of hepatocellular carcinoma in compensated cirrhotic patients

Articolo
Data di Pubblicazione:
2018
Abstract:
Background: The achievement of high rates of sustained virological response (SVR) with direct-acting antivirals (DAAs) in hepatitis C virus (HCV) infected patients will reduce decompensating terminal events. Aims: To investigate whether hepatocellular carcinoma (HCC) occurrence could change due to the DAA-induced increase in life-expectancy. Methods: A Markov model was built on clinical data of 494 cirrhotic patients and available literature to estimate probabilities of “death before HCC” and of “HCC occurrence” without and with DAA. Results: In comparison to untreated patients, DAA therapy reduced the 20-year mortality before HCC by 21.9% in patients without varices and by 21.5% in those with varices, considering an SVR of 95% and no direct effect on hepatocarcinogenesis. Tumour occurrence increased by 5%–8.2% and the proportion of HCCs diagnosed in compensated stages increased to >98%. If we consider DAA as having “anti-tumoral” effects, the benefit becomes greater, achieving a 20-year survival of 81.5% in patients without varices, and 52.2% in patients with varices. Instead, if we consider DAA as having a “pro-tumoral” effect, then, the increased incidence of HCC nullifies the survival benefits. Conclusion: DAAs drastically reduce the mortality caused by the liver function worsening, increasing the proportion of HCCs diagnosed in compensated stages. Knowledge of the DAA effect on hepatocarcinogenesis remains pivotal. © 2017 Editrice Gastroenterologica Italiana S.r.l.
Tipologia CRIS:
1.1 Articolo in rivista
Keywords:
Competing risk; Direct-acting antivirals; Hepatitis C; Hepatocellular carcinoma; Markov model; Survival benefit; Sustained virological response; Adult; Antiviral Agents; Carcinoma; Hepatocellular; Female; Hepacivirus; Hepatitis C; Humans; Incidence; Italy; Liver Neoplasms; Male; Markov Chains; Middle Aged; Risk Factors; Sustained Virologic Response; Time Factors; Hepatology; Gastroenterology
Elenco autori:
Cucchetti, Alessandro; D’Amico, Gennaro; Trevisani, Franco; Morelli, Maria Cristina; Vitale, Alessandro; Pinna, Antonio Daniele; Cescon, Matteo; Cillo, Umberto; Burra, Patrizia; Russo, Francesco P.; Mescoli, Claudia; Rendina, Maria; Lupo, Luigi G.; Losito, Francesco; Fucilli, Fabio; Brancaccio, Giusep-Pina; Persico, Marcello; Viganò, Luca; Iavarone, Massimo; D’Ambrosio, Roberta; Sangiovanni, Angelo; Renzulli, Matteo; Galati, Giovanni; Ponziani, Francesca Romana; Pompili, Maurizio; Miele, Luca; Grieco, Antonio; Rapaccini, Gianlodovico; Gasbarrini, Antonio; Sandri, Giovanni Battisa Levi; Lai, Quirino; Melandro, Fabio; Rossi, Massimo; Lenci, Ilaria; Manzia, Tommaso Maria; Tortora, Raffaella; Di Costanzo, Giovan Giuseppe; Sacco, Rodolfo; Simonetti, Natalia; Morisco, Filomena; Guarino, Maria; Cabibbo, Giuseppe; Bhoori, Carlo Sposito Sherrie; Di Sandro, Stefano; Foschi, Francesco Giuseppe; Gardini, Andrea Casadei; Nicolini, Daniele; Mazzocato, Susanna; Alba, Kostandini; Violi, Paola; Baccarani, Umberto; Pravisani, Riccardo
Autori di Ateneo:
BRANCACCIO GIUSEPPINA
Link alla scheda completa:
https://iris.unilink.it/handle/20.500.14085/34084
Pubblicato in:
DIGESTIVE AND LIVER DISEASE
Journal
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http://www.elsevier.com/wps/find/journalbibliographicinfo.cws_home/623449/description#bibliographicinfo
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