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A Long‐term Follow‐up Study on Risk Factors for Hepatocellular Carcinoma among Japanese Patients with Liver Cirrhosis

To identify virological parameters (serostatus of hepatitis B surface antigen [HBsAg] and antibodies to hepatitis C virus [anti‐HCV], HCV genotypes and HCV‐RNA titer) and other clinico‐biological and lifestyle variables that may influence or predict the development of hepatocellular carcinoma (HCC)...

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Autores principales: Tanaka, Keitaro, Sakai, Hironori, Hashizume, Makoto, Hirohata, Tomio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 1998
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5921737/
https://www.ncbi.nlm.nih.gov/pubmed/10081484
http://dx.doi.org/10.1111/j.1349-7006.1998.tb00520.x
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author Tanaka, Keitaro
Sakai, Hironori
Hashizume, Makoto
Hirohata, Tomio
author_facet Tanaka, Keitaro
Sakai, Hironori
Hashizume, Makoto
Hirohata, Tomio
author_sort Tanaka, Keitaro
collection PubMed
description To identify virological parameters (serostatus of hepatitis B surface antigen [HBsAg] and antibodies to hepatitis C virus [anti‐HCV], HCV genotypes and HCV‐RNA titer) and other clinico‐biological and lifestyle variables that may influence or predict the development of hepatocellular carcinoma (HCC) in cirrhosis, we followed 100 cirrhotic patients without HCC, who visited Kyushu University Hospital between 1985 and 1987, until the end of 1995 (follow‐up rate: 98%; average follow‐up period: 5.3 years). After elimination of 4 patients who developed HCC or were censored within the initial 6 months, 37 (39%) out of 96 patients developed HCC during follow‐up. As compared with HBsAg(+) patients, anti‐HCV(+) HBsAg(–) patients demonstrated significantly elevated HCC risk (adjusted hazard ratio [HR]=5.85, 95% confidence interval [CI] 1.65–20.67). Genotype 1 HCV infection was not associated with increased risk compared with genotype 2 (HR = 0.64, 95% CI 0.21–1.99). For genotype 1 HCV infection, patients with HCV‐RNA levels <1 Meq/ml tended to present lower risk than patients with ≥1 Meq/ml (P= 0.03). Male sex, advanced Child's class, lower serum albumin, and higher serum aminotransferase and α‐fetoprotein were also found to be strong predictors. Overall, drinking and smoking habits were not associated with significantly elevated risk. Among virological parameters, anti‐HCV positivity and, possibly high HCV‐RNA titer, were predictive of HCC occurrence in cirrhosis in our clinical setting.
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spelling pubmed-59217372018-05-11 A Long‐term Follow‐up Study on Risk Factors for Hepatocellular Carcinoma among Japanese Patients with Liver Cirrhosis Tanaka, Keitaro Sakai, Hironori Hashizume, Makoto Hirohata, Tomio Jpn J Cancer Res Article To identify virological parameters (serostatus of hepatitis B surface antigen [HBsAg] and antibodies to hepatitis C virus [anti‐HCV], HCV genotypes and HCV‐RNA titer) and other clinico‐biological and lifestyle variables that may influence or predict the development of hepatocellular carcinoma (HCC) in cirrhosis, we followed 100 cirrhotic patients without HCC, who visited Kyushu University Hospital between 1985 and 1987, until the end of 1995 (follow‐up rate: 98%; average follow‐up period: 5.3 years). After elimination of 4 patients who developed HCC or were censored within the initial 6 months, 37 (39%) out of 96 patients developed HCC during follow‐up. As compared with HBsAg(+) patients, anti‐HCV(+) HBsAg(–) patients demonstrated significantly elevated HCC risk (adjusted hazard ratio [HR]=5.85, 95% confidence interval [CI] 1.65–20.67). Genotype 1 HCV infection was not associated with increased risk compared with genotype 2 (HR = 0.64, 95% CI 0.21–1.99). For genotype 1 HCV infection, patients with HCV‐RNA levels <1 Meq/ml tended to present lower risk than patients with ≥1 Meq/ml (P= 0.03). Male sex, advanced Child's class, lower serum albumin, and higher serum aminotransferase and α‐fetoprotein were also found to be strong predictors. Overall, drinking and smoking habits were not associated with significantly elevated risk. Among virological parameters, anti‐HCV positivity and, possibly high HCV‐RNA titer, were predictive of HCC occurrence in cirrhosis in our clinical setting. Blackwell Publishing Ltd 1998-12 /pmc/articles/PMC5921737/ /pubmed/10081484 http://dx.doi.org/10.1111/j.1349-7006.1998.tb00520.x Text en
spellingShingle Article
Tanaka, Keitaro
Sakai, Hironori
Hashizume, Makoto
Hirohata, Tomio
A Long‐term Follow‐up Study on Risk Factors for Hepatocellular Carcinoma among Japanese Patients with Liver Cirrhosis
title A Long‐term Follow‐up Study on Risk Factors for Hepatocellular Carcinoma among Japanese Patients with Liver Cirrhosis
title_full A Long‐term Follow‐up Study on Risk Factors for Hepatocellular Carcinoma among Japanese Patients with Liver Cirrhosis
title_fullStr A Long‐term Follow‐up Study on Risk Factors for Hepatocellular Carcinoma among Japanese Patients with Liver Cirrhosis
title_full_unstemmed A Long‐term Follow‐up Study on Risk Factors for Hepatocellular Carcinoma among Japanese Patients with Liver Cirrhosis
title_short A Long‐term Follow‐up Study on Risk Factors for Hepatocellular Carcinoma among Japanese Patients with Liver Cirrhosis
title_sort long‐term follow‐up study on risk factors for hepatocellular carcinoma among japanese patients with liver cirrhosis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5921737/
https://www.ncbi.nlm.nih.gov/pubmed/10081484
http://dx.doi.org/10.1111/j.1349-7006.1998.tb00520.x
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