Journal
LIVER INTERNATIONAL
Volume 29, Issue 5, Pages 767-773Publisher
WILEY
DOI: 10.1111/j.1478-3231.2008.01908.x
Keywords
hepatitis B virus; hepatitis C virus; hepatocellular carcinoma; liver cirrhosis
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Funding
- National Science Council, Taiwan [95-2314-B-010-014, V95C1-009]
- Taipei Veterans General Hospital, Taipei, Taiwan
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Patients with hepatocellular carcinoma (HCC) caused by dual hepatitis B and C virus (HBV, HCV) infection may constitute a distinct disease group that is different from patients with single virus infection. This study compared the clinical characteristics and outcomes of patients with HBV, HCV and dual virus infection. A prospective database of 1215 HCC patients with chronic hepatitis B, C or dual virus infection was investigated. Patients with HCV infection (n=388) were significantly older (mean age, 69 years) than patients with dual virus (n=75, 65 years) and HBV (n=752; 60 years) infection (P < 0.0001). The male-to-female ratios for the HBV, dual virus and HCV groups were 5.2, 3.4 and 1.3 respectively (P < 0.0001). Patients in the HBV group more often had higher total tumour volume (mean, 409 cm(3)) than those in the dual virus group (244 cm(3)) and HCV (168 cm(3)) group (P < 0.0001). No significant differences of the severity of liver cirrhosis, performance status, cancer staging and tumour cell differentiation were noted among the three groups. Patients in the HCV group had a significantly poor survival in comparison with the HBV group only in the subset of patients with small tumour volume (< 50 cm(3)) in the Cox proportional hazards model (relative risk, 1.44; P=0.041). Dual HBV and HCV virus infection does not accelerate the speed of HCC formation in patients with chronic hepatitis B, and appears to have a modified course of carcinogenesis pathway that is diverted away from the biological behaviour of HBV and HCV infection.
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