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A Novel Standard for Hepatocellular Carcinoma Screening Intensity After Hepatitis C Elimination

PURPOSE: To investigate long-term incidence of hepatocellular carcinoma (HCC) and the factors associated with HCC occurrence after achieving sustained virological response (SVR) by direct-acting antiviral agent (DAA) treatment for hepatitis C virus (HCV). METHODS: A total of 476 patients (male 227,...

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Autores principales: Miyasaka, Akio, Yoshida, Yuichi, Suzuki, Akiko, Sawara, Kei, Takikawa, Yasuhiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8636695/
https://www.ncbi.nlm.nih.gov/pubmed/34866934
http://dx.doi.org/10.2147/IJGM.S344492
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author Miyasaka, Akio
Yoshida, Yuichi
Suzuki, Akiko
Sawara, Kei
Takikawa, Yasuhiro
author_facet Miyasaka, Akio
Yoshida, Yuichi
Suzuki, Akiko
Sawara, Kei
Takikawa, Yasuhiro
author_sort Miyasaka, Akio
collection PubMed
description PURPOSE: To investigate long-term incidence of hepatocellular carcinoma (HCC) and the factors associated with HCC occurrence after achieving sustained virological response (SVR) by direct-acting antiviral agent (DAA) treatment for hepatitis C virus (HCV). METHODS: A total of 476 patients (male 227, female 249; median age 68) with chronic HCV infection who were treated with DAAs and achieved SVR were analyzed. The incidence of HCC and factors related to the development of HCC after HCV elimination were evaluated. RESULTS: The median observation period was 46.4 months. During this period, 40 patients developed HCC. The incidence rates of HCC were 3.7%, 6.0%, 7.1%, 9.3%, and 10.6% at 1, 2, 3, 4, and 5 years post-SVR12, respectively. Multivariate analysis with pre-treatment factors revealed that platelet count, α-fetoprotein, fibrosis-4 (Fib-4) index, and previous HCC history were independent factors that contributed to development of HCC post-SVR following DAA treatment. Of these factors, previous HCC history was the most significant, followed by Fib-4 index. Using these two factors, a novel scoring system was established. The presence of previous HCC history was scored as 2, and then, the absence of previous HCC history was stratified by Fib-4 index (≥3.07, 1; <3.07, 0). The HCC occurrence rate at 5 years was 0.4% in the 0-point group, 6.8% in the 1-point group, and 55.6% in the 2-point group, respectively. CONCLUSION: Fib-4 index and previous HCC history were independent predictors for development of HCC after DAA treatment. Patients with these risk factors require careful observation.
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spelling pubmed-86366952021-12-02 A Novel Standard for Hepatocellular Carcinoma Screening Intensity After Hepatitis C Elimination Miyasaka, Akio Yoshida, Yuichi Suzuki, Akiko Sawara, Kei Takikawa, Yasuhiro Int J Gen Med Original Research PURPOSE: To investigate long-term incidence of hepatocellular carcinoma (HCC) and the factors associated with HCC occurrence after achieving sustained virological response (SVR) by direct-acting antiviral agent (DAA) treatment for hepatitis C virus (HCV). METHODS: A total of 476 patients (male 227, female 249; median age 68) with chronic HCV infection who were treated with DAAs and achieved SVR were analyzed. The incidence of HCC and factors related to the development of HCC after HCV elimination were evaluated. RESULTS: The median observation period was 46.4 months. During this period, 40 patients developed HCC. The incidence rates of HCC were 3.7%, 6.0%, 7.1%, 9.3%, and 10.6% at 1, 2, 3, 4, and 5 years post-SVR12, respectively. Multivariate analysis with pre-treatment factors revealed that platelet count, α-fetoprotein, fibrosis-4 (Fib-4) index, and previous HCC history were independent factors that contributed to development of HCC post-SVR following DAA treatment. Of these factors, previous HCC history was the most significant, followed by Fib-4 index. Using these two factors, a novel scoring system was established. The presence of previous HCC history was scored as 2, and then, the absence of previous HCC history was stratified by Fib-4 index (≥3.07, 1; <3.07, 0). The HCC occurrence rate at 5 years was 0.4% in the 0-point group, 6.8% in the 1-point group, and 55.6% in the 2-point group, respectively. CONCLUSION: Fib-4 index and previous HCC history were independent predictors for development of HCC after DAA treatment. Patients with these risk factors require careful observation. Dove 2021-11-27 /pmc/articles/PMC8636695/ /pubmed/34866934 http://dx.doi.org/10.2147/IJGM.S344492 Text en © 2021 Miyasaka et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Miyasaka, Akio
Yoshida, Yuichi
Suzuki, Akiko
Sawara, Kei
Takikawa, Yasuhiro
A Novel Standard for Hepatocellular Carcinoma Screening Intensity After Hepatitis C Elimination
title A Novel Standard for Hepatocellular Carcinoma Screening Intensity After Hepatitis C Elimination
title_full A Novel Standard for Hepatocellular Carcinoma Screening Intensity After Hepatitis C Elimination
title_fullStr A Novel Standard for Hepatocellular Carcinoma Screening Intensity After Hepatitis C Elimination
title_full_unstemmed A Novel Standard for Hepatocellular Carcinoma Screening Intensity After Hepatitis C Elimination
title_short A Novel Standard for Hepatocellular Carcinoma Screening Intensity After Hepatitis C Elimination
title_sort novel standard for hepatocellular carcinoma screening intensity after hepatitis c elimination
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8636695/
https://www.ncbi.nlm.nih.gov/pubmed/34866934
http://dx.doi.org/10.2147/IJGM.S344492
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