Volume 49, Issue 12 pp. 1441-1450
Original Article

Long-term outcome of hepatocellular carcinoma occurrence, esophageal varices exacerbation, and mortality in hepatitis C virus-related liver cirrhosis after interferon-based therapy

Nobuhiko Ogasawara

Corresponding Author

Nobuhiko Ogasawara

Department of Hepatology and Okinaka Memorial Institute for Medical Research, Toranomon Hospital, Tokyo, Japan

Correspondence: Dr Nobuhiko Ogasawara, Department of Hepatology, Toranomon Hospital, 2-2-2 Toranomon, Minato-ku, Tokyo 105-0001, Japan. Email: [email protected]Search for more papers by this author
Satoshi Saitoh

Satoshi Saitoh

Department of Hepatology and Okinaka Memorial Institute for Medical Research, Toranomon Hospital, Tokyo, Japan

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Norio Akuta

Norio Akuta

Department of Hepatology and Okinaka Memorial Institute for Medical Research, Toranomon Hospital, Tokyo, Japan

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Shunichiro Fujiyama

Shunichiro Fujiyama

Department of Hepatology and Okinaka Memorial Institute for Medical Research, Toranomon Hospital, Tokyo, Japan

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Yusuke Kawamura

Yusuke Kawamura

Department of Hepatology and Okinaka Memorial Institute for Medical Research, Toranomon Hospital, Tokyo, Japan

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Hitomi Sezaki

Hitomi Sezaki

Department of Hepatology and Okinaka Memorial Institute for Medical Research, Toranomon Hospital, Tokyo, Japan

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Tetsuya Hosaka

Tetsuya Hosaka

Department of Hepatology and Okinaka Memorial Institute for Medical Research, Toranomon Hospital, Tokyo, Japan

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Masahiro Kobayashi

Masahiro Kobayashi

Department of Hepatology and Okinaka Memorial Institute for Medical Research, Toranomon Hospital, Tokyo, Japan

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Fumitaka Suzuki

Fumitaka Suzuki

Department of Hepatology and Okinaka Memorial Institute for Medical Research, Toranomon Hospital, Tokyo, Japan

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Yoshiyuki Suzuki

Yoshiyuki Suzuki

Department of Hepatology and Okinaka Memorial Institute for Medical Research, Toranomon Hospital, Tokyo, Japan

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Yasuji Arase

Yasuji Arase

Department of Hepatology and Okinaka Memorial Institute for Medical Research, Toranomon Hospital, Tokyo, Japan

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Kenji Ikeda

Kenji Ikeda

Department of Hepatology and Okinaka Memorial Institute for Medical Research, Toranomon Hospital, Tokyo, Japan

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Hiromitsu Kumada

Hiromitsu Kumada

Department of Hepatology and Okinaka Memorial Institute for Medical Research, Toranomon Hospital, Tokyo, Japan

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First published: 01 August 2019
Citations: 11
Conflict of interest: H Kumada has received honoraria from MSD, Bristol-Myers Squibb, Gilead Sciences, AbbVie Inc, and Dainippon Sumitomo Pharma. N Akuta has received an honorarium from Bristol-Myers Squibb and AbbVie. Y Suzuki has received an honorarium from Bristol-Myers Squibb and AbbVie. M Kobayashi has received an honorarium from Eisai. F Suzuki has received an honorarium from Bristol-Myers Squibb and AbbVie. K Ikeda has received honoraria from Dainippon Sumitomo Pharma and Eisai. All other authors declare that they have no conflicts of interest.

Abstract

Aim

The long-term effects of sustained virologic response (SVR) to antiviral therapy on the risk of liver complications, such as exacerbation of esophageal varices (EV), hepatocellular carcinoma (HCC), malignant lymphoma, and liver-related and overall death in hepatitis C virus (HCV)-infected patients with liver cirrhosis are not fully known.

Methods

These risks were evaluated during long-term follow up of 457 patients with HCV-related Child–Pugh Class A liver cirrhosis without history of HCC.

Results

The respective cumulative 5- and 10-year rates of EV exacerbation were 2.0% and 3.1%. Multivariate analysis identified the presence of EVs, thrombocytopenia at baseline. and alcohol intake as significant independent predictors of EV exacerbation before and after SVR. The cumulative 5- and 10-year rates of HCC were 6.8% and 10.2%, respectively. Male sex and the presence of EV were significant independent determinants of HCC before and after SVR. Although the cumulative 5-year HCC recurrence rate was 49.4%, the overall survival rate since HCC was 73.6% at 5 years. The overall survival rates since SVR were 98.7% and 93.6% at 5 and 10 years, respectively. Progression of HCC was the most frequent all-cause mortality, but none of the patients died of liver decompensation. Male sex and Fibrosis-4 index of ≥3.0 after SVR were significant and independent predictors of mortality.

Conclusion

Patients with HCV remain at risk of HCC for >10 years after achieving SVR, and HCC is the most common cause of mortality. We recommend long-term surveillance of cirrhotic patients with HCV, even after achieving SVR.

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