Hepatocellular Carcinoma

AASLD Hepatocellular Carcinoma

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Key Points ÎThe incidence of hepatocellular carcinoma (HCC) is rising in many countries. ÎCare of the patient with HCC involves physicians from different disciplines including hepatologists, surgeons, liver transplant teams, oncologists, interventional radiologists, and to some extent radiation oncologists. ÎAssessing the degree of liver function impairment prior to, during and after therapy is important since HCC usually appears in the setting of underlying liver disease. Surveillance and Assessment Table 1. Groups for Whom HCC Surveillance in Recommended or in Whom the Risk of HCC is Increased, but in Whom Efficacy of Surveillance Has Not Been Demonstrated Population Group Surveillance recommended Cirrhotic hepatitis B carriers Hepatitis C cirrhosis Stage 4 primary biliary cirrhosis Genetic hemachromatosis and cirrhosis Alpha 1-antitrypsin deficiency and cirrhosis Other cirrhosis Asian male hepatitis B carriers > age 40 Asian female hepatitis B carriers > age 50 Hepatitis B carrier with family history of HCC African/North American Blacks with hepatitis B Surveillance benefit uncertain Hepatitis C and stage 3 fibrosis Non-cirrhotic NAFLD Hepatitis B carriers < 40 (males) or < 50 (females) Threshold Incidence for Efficacy of Surveillance (> 0.25 LYG) (%/year) 0.2-1.5 1.5 1.5 1.5 1.5 1.5 0.2 0.2 0.2 0.2 1.5 1.5 0.2 Incidence of HCC 3-8%/year 3-5%/year 3-5%/year Unknown, but probably > 1.5%/year Unknown, but probably > 1.5%/year Unknown 0.4-0.6%/year 0.3-0.6%/year Incidence higher than without family history HCC occurs at a younger age < 1.5%/year < 1.5%/year < 0.2%/year

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