Hepatitis D virus (HDV) has been officially classified as a carcinogenic virus by the International Agency for Research on Cancer (IARC), part of the World Health Organization (WHO), putting it in the same category as hepatitis B and C viruses regarding cancer risk.
Key points regarding Hepatitis D and cancer risk are:
HDV can only infect people already infected with hepatitis B virus (HBV).
Co-infection with HDV and HBV significantly increases the risk of developing liver cancer (hepatocellular carcinoma) by 2 to 6 times compared to hepatitis B infection alone.
Around 75% of people chronically infected with HDV develop liver cirrhosis within 15 years, a precursor condition that can lead to liver cancer.
The combined infection causes more aggressive liver disease progression, with more rapid progression to cirrhosis, liver failure, and cancer, making hepatitis D the most severe form of viral hepatitis.
Transmission occurs through blood and bodily fluids similar to HBV, and prevention is mainly through hepatitis B vaccination, which indirectly protects against hepatitis D.
Despite hepatitis D being less common than hepatitis B alone, its high carcinogenic potential means it has a disproportionately severe impact on liver cancer burden globally.
Treatments for hepatitis D
Bulevirtide is the only currently approved and widely used therapy with proven effectiveness and a good safety profile for chronic hepatitis D.
It achieves viral suppression in most patients and improves liver inflammation.
Other promising treatments are in advanced clinical trials and may soon provide additional options.
These advances make hepatitis D a potentially manageable disease going forward, especially when combined with hepatitis B vaccination for prevention.