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Updated: May 15, 2026

Real-Time Polymerase Chain Reaction-Based Detection and Quantification of Hepatitis B Virus DNA
Published on: December 15, 2023
Epidemiology of hepatitis B-associated hepatocellular carcinoma in Victoria
M Sinclair1, S Roberts, W Kemp
1Department of Gastroenterology and Hepatology, Royal Melbourne Hospital, Heidelberg, Victoria, Australia.
Insights
Most patients with hepatitis B (HBV)-associated liver cancer (HCC) in Melbourne have cirrhosis. Characteristics of HCC were similar in cirrhotic and non-cirrhotic patients, highlighting screening needs.
Area of Science:
- Hepatology
- Oncology
- Viral Hepatitis Research
Background:
- Chronic hepatitis B virus (HBV) infection is a primary risk factor for hepatocellular carcinoma (HCC).
- Limited data exists on the prevalence and traits of cirrhosis in HBV-associated HCC cases.
Purpose of the Study:
- To compare demographic, viral, and tumor characteristics of HBV-associated HCC.
- To evaluate differences between patients with and without cirrhosis in an Australian cohort.
Main Methods:
- Review of 197 HBV-associated HCC cases from Melbourne teaching hospitals.
- Assessment of patient demographics, HBV viral markers, cirrhosis status, alpha-fetoprotein levels, and tumor size.
- Recording of diagnosis mode (surveillance vs. symptoms) and treatment type.
Main Results:
- The majority of HBV-HCC patients (87%) had cirrhosis.
- Patients with cirrhosis were older (median 60 vs. 52 years).
- Asian patients had a higher likelihood of HCC without cirrhosis compared to Europeans (17% vs. 6%).
- Tumor size >5 cm and diagnosis via symptoms were common (34% and 47% respectively).
Conclusions:
- Cirrhosis is prevalent in Melbourne's HBV-associated HCC population.
- HCC characteristics were largely similar between cirrhotic and non-cirrhotic patients.
- Delayed diagnosis through symptoms and large tumor size underscore the importance of vigilant screening for HBV-HCC.
Background:
Chronic hepatitis B (HBV) and cirrhosis are major risk factors for hepatocellular carcinoma (HCC). The proportion and characteristics of cases with cirrhosis are not well documented.
Aim:
Our aim was to compare demographic, viral and tumour characteristics of HBV-associated HCC in an Australian cohort, in patients with and without cirrhosis.
Methods:
Existing HCC databases at six Melbourne teaching hospitals were reviewed for cases associated with HBV. Patient demographics, HBV viral characteristics, presence of cirrhosis, serum alpha-fetoprotein and tumour size were assessed. Mode of diagnosis was recorded through surveillance or symptoms, and treatment was either palliative, percutaneous or surgical.
Results:
We identified 197 cases of HBV-related HCC. The mean age was 57.9 ± 12.9 years; 83% were male, and 55.3% and 35.3% were of Asian and European descent respectively. Of 168 patient with available data, 146 (87%) had cirrhosis versus 22 (13%) without. Patients with cirrhosis tended to be older (median 60 vs 52 years, P = 0.078). Asian patients were more likely to have HCC without cirrhosis than Europeans (17% vs 6%, P = 0.04). There were no other differences identified between cirrhotic and non-cirrhotic patients. Thirty-four per cent of patients had tumours greater than 5 cm at diagnosis, and 47% were diagnosed after presenting with symptoms. Twelve patients with HBV-HCC were outside current screening guidelines.
Conclusion:
Most patients in Melbourne with HBV-associated HCC have cirrhosis. HCC characteristics in non-cirrhotic and cirrhotic patients were similar. The large number of patients detected through symptoms and with large tumours reinforces the need for vigilance in screening.
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