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Direct acting antivirals treatment for hepatitis C virus infection does not increase the incidence of de novo hepatocellular carcinoma occurrence: Results from an Italian real-life cohort (LINA cohort)
The effectiveness of direct-acting antivirals (DAAs) against hepatitis C virus (HCV) infection is ascertained. However, some authors raised the issue of an increased incidence of de novo hepatocellular carcinoma (HCC) in patients treated with DAAs. Aim of the study was to evaluate the rate of HCC oc...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7015572/ https://www.ncbi.nlm.nih.gov/pubmed/32028404 http://dx.doi.org/10.1097/MD.0000000000018948 |
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author | Buonomo, Antonio Riccardo Scotto, Riccardo Coppola, Carmine Pinchera, Biagio Viceconte, Giulio Rapillo, Costanza Maria Staiano, Laura Saturnino, Mariarosaria Scarano, Ferdinando Portunato, Federica Pisaturo, Mariantonietta De Pascalis, Stefania Martini, Salvatore Tosone, Grazia Nappa, Salvatore Coppola, Nicola Gentile, Ivan |
author_facet | Buonomo, Antonio Riccardo Scotto, Riccardo Coppola, Carmine Pinchera, Biagio Viceconte, Giulio Rapillo, Costanza Maria Staiano, Laura Saturnino, Mariarosaria Scarano, Ferdinando Portunato, Federica Pisaturo, Mariantonietta De Pascalis, Stefania Martini, Salvatore Tosone, Grazia Nappa, Salvatore Coppola, Nicola Gentile, Ivan |
author_sort | Buonomo, Antonio Riccardo |
collection | PubMed |
description | The effectiveness of direct-acting antivirals (DAAs) against hepatitis C virus (HCV) infection is ascertained. However, some authors raised the issue of an increased incidence of de novo hepatocellular carcinoma (HCC) in patients treated with DAAs. Aim of the study was to evaluate the rate of HCC occurrence in a real-life cohort of patients who received anti-HCV treatment with DAAs. A prospective multicentre study was conducted. All adult patients with HCV infection who received treatment between March 2015 and December 2017 in 4 hospital of Campania region (South Italy) with at least 6 months of follow-up were enrolled. A total of 323 patients were included in the study. Most patients had HCV genotype 1b (61.8%). The overall SVR12 rate was 95.5%. Median time of observation was 10 months. The incidence rate of HCC was 0.2 per 100 person-months (crude incidence rate 3.4%, 95 confidence interval: 1.5%–5.3%). The median time for HCC occurrence was 11 months. HCC occurrence rate was significantly higher among patients who did not achieve SVR12 compared with patients who did (28.6% vs 2.8%, P < 0.05). No patient with F0-F3 fibrosis developed HCC. Among patients with cirrhosis, at the multivariate time-to-event analysis, no covariates were independently associated with the risk of HCC occurrence. Treatment with DAAs did not increase the risk of HCC occurrence. Patients who achieved SVR12 had a lower rate of HCC occurrence. Further studies are needed to estimate the incidence and the risk for HCC in the long-term follow-up among patients undergoing treatment with DAAs. |
format | Online Article Text |
id | pubmed-7015572 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-70155722020-02-26 Direct acting antivirals treatment for hepatitis C virus infection does not increase the incidence of de novo hepatocellular carcinoma occurrence: Results from an Italian real-life cohort (LINA cohort) Buonomo, Antonio Riccardo Scotto, Riccardo Coppola, Carmine Pinchera, Biagio Viceconte, Giulio Rapillo, Costanza Maria Staiano, Laura Saturnino, Mariarosaria Scarano, Ferdinando Portunato, Federica Pisaturo, Mariantonietta De Pascalis, Stefania Martini, Salvatore Tosone, Grazia Nappa, Salvatore Coppola, Nicola Gentile, Ivan Medicine (Baltimore) 4500 The effectiveness of direct-acting antivirals (DAAs) against hepatitis C virus (HCV) infection is ascertained. However, some authors raised the issue of an increased incidence of de novo hepatocellular carcinoma (HCC) in patients treated with DAAs. Aim of the study was to evaluate the rate of HCC occurrence in a real-life cohort of patients who received anti-HCV treatment with DAAs. A prospective multicentre study was conducted. All adult patients with HCV infection who received treatment between March 2015 and December 2017 in 4 hospital of Campania region (South Italy) with at least 6 months of follow-up were enrolled. A total of 323 patients were included in the study. Most patients had HCV genotype 1b (61.8%). The overall SVR12 rate was 95.5%. Median time of observation was 10 months. The incidence rate of HCC was 0.2 per 100 person-months (crude incidence rate 3.4%, 95 confidence interval: 1.5%–5.3%). The median time for HCC occurrence was 11 months. HCC occurrence rate was significantly higher among patients who did not achieve SVR12 compared with patients who did (28.6% vs 2.8%, P < 0.05). No patient with F0-F3 fibrosis developed HCC. Among patients with cirrhosis, at the multivariate time-to-event analysis, no covariates were independently associated with the risk of HCC occurrence. Treatment with DAAs did not increase the risk of HCC occurrence. Patients who achieved SVR12 had a lower rate of HCC occurrence. Further studies are needed to estimate the incidence and the risk for HCC in the long-term follow-up among patients undergoing treatment with DAAs. Wolters Kluwer Health 2020-02-07 /pmc/articles/PMC7015572/ /pubmed/32028404 http://dx.doi.org/10.1097/MD.0000000000018948 Text en Copyright © 2020 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nc/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial License 4.0 (CCBY-NC), where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc/4.0 |
spellingShingle | 4500 Buonomo, Antonio Riccardo Scotto, Riccardo Coppola, Carmine Pinchera, Biagio Viceconte, Giulio Rapillo, Costanza Maria Staiano, Laura Saturnino, Mariarosaria Scarano, Ferdinando Portunato, Federica Pisaturo, Mariantonietta De Pascalis, Stefania Martini, Salvatore Tosone, Grazia Nappa, Salvatore Coppola, Nicola Gentile, Ivan Direct acting antivirals treatment for hepatitis C virus infection does not increase the incidence of de novo hepatocellular carcinoma occurrence: Results from an Italian real-life cohort (LINA cohort) |
title | Direct acting antivirals treatment for hepatitis C virus infection does not increase the incidence of de novo hepatocellular carcinoma occurrence: Results from an Italian real-life cohort (LINA cohort) |
title_full | Direct acting antivirals treatment for hepatitis C virus infection does not increase the incidence of de novo hepatocellular carcinoma occurrence: Results from an Italian real-life cohort (LINA cohort) |
title_fullStr | Direct acting antivirals treatment for hepatitis C virus infection does not increase the incidence of de novo hepatocellular carcinoma occurrence: Results from an Italian real-life cohort (LINA cohort) |
title_full_unstemmed | Direct acting antivirals treatment for hepatitis C virus infection does not increase the incidence of de novo hepatocellular carcinoma occurrence: Results from an Italian real-life cohort (LINA cohort) |
title_short | Direct acting antivirals treatment for hepatitis C virus infection does not increase the incidence of de novo hepatocellular carcinoma occurrence: Results from an Italian real-life cohort (LINA cohort) |
title_sort | direct acting antivirals treatment for hepatitis c virus infection does not increase the incidence of de novo hepatocellular carcinoma occurrence: results from an italian real-life cohort (lina cohort) |
topic | 4500 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7015572/ https://www.ncbi.nlm.nih.gov/pubmed/32028404 http://dx.doi.org/10.1097/MD.0000000000018948 |
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