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Clinical characteristics of patients who developed hepatocellular carcinoma after hepatitis C virus eradication with interferon therapy: current status in Japan.

Authors :
Sato A
Sata M
Ikeda K
Kumada T
Izumi N
Asahina Y
Osaki Y
Chayama K
Kaneko S
Sakai A
Onji M
Hiasa Y
Omura T
Ozeki I
Yokosuka O
Shiina S
Itsubo M
Nishiguchi S
Hirano K
Ide T
Sakisaka S
Yamasaki T
Hidaka I
Tanaka M
Kim SR
Ichida T
Source :
Internal medicine (Tokyo, Japan) [Intern Med] 2013; Vol. 52 (24), pp. 2701-6.
Publication Year :
2013

Abstract

Objective: We attempted to elucidate the clinical features of chronic hepatitis C patients who develop hepatocellular carcinoma (HCC) after achieving a sustained viral response (SVR) to interferon (IFN) therapy.<br />Methods: The clinical features of 130 patients at 19 hospitals who developed HCC after obtaining an SVR were retrospectively reviewed.<br />Results: Overall, 107 (82%) of the 130 patients were men, with 92 (71%) being ≥60 years of age and 76, 38 and 16 developing HCC within 5, 5-10 and 10-16.9 years after IFN therapy, respectively. Before receiving IFN therapy, 92 (71%) patients had cirrhosis and/or a low platelet count (<15×10(4) cells/μL). Lower albumin (<3.9 g/dL) and higher alpha fetoprotein (AFP) (≥10 ng/mL) levels were identified in a multivariate analysis to be independent variables of the development of HCC within five years after IFN therapy. Among 4,542 SVR patients, HCC occurred in 109 (2.4%) during a 5.5-year follow-up period, thus resulting in an occurrence rate of 4.6% for men and 0.6% for women.<br />Conclusion: SVR patients with lower albumin or higher AFP levels require careful assessments to prevent early HCC development after IFN therapy. HCC occurrence within >10 years of IFN therapy is not uncommon, and the risk factors remain uncertain, thus suggesting that all SVR patients should undergo long-term follow-up examinations for HCC development.

Details

Language :
English
ISSN :
1349-7235
Volume :
52
Issue :
24
Database :
MEDLINE
Journal :
Internal medicine (Tokyo, Japan)
Publication Type :
Academic Journal
Accession number :
24334571
Full Text :
https://doi.org/10.2169/internalmedicine.52.1180