Overcoming disparities in hepatocellular carcinoma outcomes in First Nations Australians: a strategic plan for action

Jessica Howell, Troy Combo, Paula Binks, Kylie Bragg, Sarah Bukulatjpi, Kirsty Campbell, Paul J. Clark, Melissa Carroll, Jane Davies, Teresa de Santis, Kate R. Muller, Bella Nguyen, John K. Olynyk, Nicholas Shackel, Patricia C. Valery, Alan J. Wigg, Jacob George, Stuart K. Roberts

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Abstract

Every year, about 1800 Australians die of hepatocellular carcinoma (HCC), the most common type of primary liver cancer.

Aboriginal and Torres Strait Islander peoples of Australia (hereon respectfully referred to as First Nations Australians) are 2.5 times more likely to develop HCC and 1.4 times more likely to die from HCC than non-Indigenous Australians.

First Nations Australians with HCC have a 9% five-year survival rate compared with 23% for non-Indigenous Australians,2 and are half as likely to be diagnosed with early-stage HCC and receive curative therapy.2 This is driven by First Nations Australians being adversely affected by social, cultural and commercial determinants of health stemming from colonisation, racism and remoteness.
Original languageEnglish
Pages (from-to)230-235
Number of pages6
JournalMedical Journal of Australia
Volume221
Issue number5
Early online date6 Aug 2024
DOIs
Publication statusPublished - 2 Sept 2024

Keywords

  • hepatocellular carcinoma
  • First Nations Australians
  • liver cancer
  • Determinants of health and social inequalities.
  • Chronic liver disease

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