HCC screening is recommended for people living with hepatitis B who are willing* and suitable** to receive HCC treatment in these groups:
- People with cirrhosis including those with HBsAg loss
- Asian-Pacific males > 40 years
- Asian-Pacific females > 50 years
- Sub-Saharan African people > 20 years
- Aboriginal people > 50 years
- Aboriginal people with high-risk features*** > 40 years
- Anyone aged > 40 years with a family history of HCC (first-degree relatives)
Consider offering HCC surveillance 10 years prior to earliest case in a family.
* ‘Willing’ means someone who is willing to receive a HCC diagnosis and if diagnosed, to undergo HCC treatment.
** ‘Suitable’ is defined as: someone who is well enough to receive HCC treatment (including patients with Child-Pugh stage A or B cirrhosis or patients with Child-Pugh stage C awaiting liver transplantation) and is without significant comorbidities and therefore has a non-HCC-related life expectancy of > 6 months.
**High-risk features include: a family history of HCC or a high-risk HBV genotype individually confirmed (eg C4) or epidemiologically likely.
The increased risk of hepatitis-B-related liver cancer among Aboriginal peoples highlights the enduring traumatic legacy of colonisation, recognising the historical disadvantage perpetuated by institutional racism and systemic failures that collectively contribute to health disparities between Aboriginal peoples and non-Indigenous Australians.