Cancer Causes & Control

, Volume 14, Issue 10, pp 995-1000

First online:

Spontaneous clearance of high-titer serum HBV DNA and risk of hepatocellular carcinoma in a Chinese population

  • Rebecca A. HarrisAffiliated withDivision of Population Science, Fox Chase Cancer Center
  • , Gang ChenAffiliated withDivision of Population Science, Fox Chase Cancer Center
  • , Wen Yao LinAffiliated withHaimen City Centers for Disease Control
  • , Fu Min ShenAffiliated withFudan University School of Public Health
  • , W. Thomas LondonAffiliated withDivision of Population Science, Fox Chase Cancer Center
  • , Alison A. EvansAffiliated withDivision of Population Science, Fox Chase Cancer Center Email author 

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Chronic hepatitis B virus (HBV) carriers with high-titer viremia (>105 virions/ml) are at increased risk for hepatocellular carcinoma (HCC). The aim of this study was to determine the relationship between clearance of high-titer viremia and subsequent risk of HCC. The study population was a prospective cohort of 114 adults from Haimen City, China, all HBV DNA(+) at study entry and followed for 797.8 person-years in total. During follow-up, 54 (47.4%) subjects spontaneously cleared high-titer viremia at least once. Of these, 27 were considered to have undergone stable seroconversion, 16 were considered unstable (12 reversions to HBV DNA positivity and 4 multiple clearances), and 11 did not have sufficient follow-up to determine stability. Of the 114 persons, 26 (22.8%) died during follow-up, 21 (18.4%) from HCC. Using Cox proportional hazards models, the RR of HCC death associated with seroconversion was 2.8 (95% CI = 1.1–7.4), controlling for age, sex, family HCC history, history of acute hepatitis, alcohol use and cigarette smoking. In conclusion, fluctuations of high-titer viremia may indicate increased hepatocellular damage and at least short-term increases in HCC risk. Long-term longitudinal studies are needed to clarify this relationship and its potential usefulness as a prognostic marker in chronic HBV infection.

Cox proportional hazards regression HBV DNA hepatitis B virus hepatocellular carcinoma risk factors viral load