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Risk of development of hepatocellular carcinoma in patients with NASH-related cirrhosis
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Background and aims:
The risk of development of hepatocellular carcinoma (HCC) in hepatitis B virus (HBV) and hepatitis C virus (HCV) infection is well established and is being recognized increasingly in non-alcoholic steatohepatitis (NASH)-related cirrhosis. This study aimed to assess the risk of development of HCC in patients with NASH-related cirrhosis.
Methods:
From January 2010 to October 2011, we prospectively enrolled 585 patients with liver cirrhosis (men:women ratio 4.4:1, mean age 50.1±6.1 years, aetiology HBV 19%, HCV 14.2%, NASH-related 7%, cryptogenic cirrhosis 17.8%, already diagnosed cirrhosis 48.2%, and the remaining were newly diagnosed cases). The cumulative follow-up was for 5.9±0.5, 6.1+0.8 and 6.8+1.2 years for HBV, HCV and NASH-related cirrhosis, respectively. Patients with advanced cirrhosis, Child class C and associated comorbid conditions where survival was <1 year were excluded from the study. The remaining patients were followed up 6-monthly with ultrasound examination and alpha-fetoprotein (AFP) test. Patients suspected of HCC underwent triple-phase computed tomography (CT) scan and liver biopsy was done to confirm the diagnosis.
Results:
A total of 54 patients developed HCC, of which 26 had HBV, 14 had HCV, 9 hadcryptogenic and 6 had- NASH-related cirrhosis. The annual rate of development of HCC was 1.5%, 3.6%, 0.6% and 0.46 in HBV, HCV, cryptogenic and NASH-related cirrhosis, respectively.
Conclusions:
The incidence of HCC was highest in HCV and lowest in NASH-related cirrhosis. These figures suggest an intermediate risk of development of HCC when compared to western countries and Japan.
Ovid Technologies (Wolters Kluwer Health)
Title: Risk of development of hepatocellular carcinoma in patients with NASH-related cirrhosis
Description:
Background and aims:
The risk of development of hepatocellular carcinoma (HCC) in hepatitis B virus (HBV) and hepatitis C virus (HCV) infection is well established and is being recognized increasingly in non-alcoholic steatohepatitis (NASH)-related cirrhosis.
This study aimed to assess the risk of development of HCC in patients with NASH-related cirrhosis.
Methods:
From January 2010 to October 2011, we prospectively enrolled 585 patients with liver cirrhosis (men:women ratio 4.
4:1, mean age 50.
1±6.
1 years, aetiology HBV 19%, HCV 14.
2%, NASH-related 7%, cryptogenic cirrhosis 17.
8%, already diagnosed cirrhosis 48.
2%, and the remaining were newly diagnosed cases).
The cumulative follow-up was for 5.
9±0.
5, 6.
1+0.
8 and 6.
8+1.
2 years for HBV, HCV and NASH-related cirrhosis, respectively.
Patients with advanced cirrhosis, Child class C and associated comorbid conditions where survival was <1 year were excluded from the study.
The remaining patients were followed up 6-monthly with ultrasound examination and alpha-fetoprotein (AFP) test.
Patients suspected of HCC underwent triple-phase computed tomography (CT) scan and liver biopsy was done to confirm the diagnosis.
Results:
A total of 54 patients developed HCC, of which 26 had HBV, 14 had HCV, 9 hadcryptogenic and 6 had- NASH-related cirrhosis.
The annual rate of development of HCC was 1.
5%, 3.
6%, 0.
6% and 0.
46 in HBV, HCV, cryptogenic and NASH-related cirrhosis, respectively.
Conclusions:
The incidence of HCC was highest in HCV and lowest in NASH-related cirrhosis.
These figures suggest an intermediate risk of development of HCC when compared to western countries and Japan.
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