Hepatocellular carcinoma is associated with an increased risk of hepatitis B virus recurrence after liver transplantation

Gastroenterology. 2008 Jun;134(7):1890-9; quiz 2155. doi: 10.1053/j.gastro.2008.02.064. Epub 2008 Mar 4.

Abstract

Background & aims: Hepatitis B virus (HBV) recurrence after orthotopic liver transplantation (OLT) is significantly reduced by prophylaxis with hyperimmune antibody to hepatitis B surface antigen (anti-HBs) globulins (HBIG) and antiviral drugs. The role of hepatocellular carcinoma (HCC) in HBV recurrence remains unclear. We investigated the association between HCC pre-OLT and HBV recurrence post-OLT.

Methods: We studied 99 hepatitis B surface antigen-positive patients who underwent OLT for cirrhosis. The median follow-up period was 43 months. All patients received HBIG, and 51 also received lamivudine and/or adefovir. Of these 99 patients, 31 had HCC before OLT. Total HBV DNA and covalently closed circular (ccc)-DNA were measured in tumor and nontumor tissues from the explanted livers of 16 of these 31 HCC patients and, also, in a context of tumor recurrence, in 3 patients who developed HBV/HCC recurrence.

Results: Fourteen patients (14.1%) developed HBV recurrence within a median period of 15 months post-OLT. HCC at OLT, a pre-OLT HBV DNA viral load > or = 100,000 copies/mL, and HBIG monoprophylaxis were independently associated with HBV recurrence post-OLT. Eleven out of the 31 patients with HCC at OLT presented with HBV recurrence and 3 out of the 68 patients without HCC had HBV recurrence (P < .0001). HBV recurrence was more frequent in patients who developed HCC recurrence (7/8 patients, 87.5%) than in those who did not (4/23 patients, 17.4%) (P < .0001). In the 16 explanted livers, cccDNA was detectable in HCC cells in 11 and in nontumor cells in 12. cccDNA was detected in a context of HCC recurrence in 2 of the 3 patients tested who developed HBV/HCC recurrence.

Conclusions: The associations of HCC pre-OLT, and HCC recurrence with HBV recurrence post-OLT, and the detection of HBV DNA and cccDNA in HCC suggest that HBV replication in tumor cells may contribute to HBV recurrence post-OLT.

Publication types

  • Clinical Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenine / analogs & derivatives
  • Adenine / therapeutic use
  • Adolescent
  • Adult
  • Aged
  • Antiviral Agents / therapeutic use
  • Carcinoma, Hepatocellular / drug therapy
  • Carcinoma, Hepatocellular / surgery
  • Carcinoma, Hepatocellular / virology*
  • DNA, Circular / analysis
  • DNA, Viral / analysis
  • Female
  • Follow-Up Studies
  • Hepatitis B / complications
  • Hepatitis B / diagnosis
  • Hepatitis B / drug therapy
  • Hepatitis B / etiology*
  • Hepatitis B / surgery
  • Hepatitis B Surface Antigens / analysis
  • Hepatitis B virus* / genetics
  • Hepatitis B virus* / growth & development
  • Hepatitis B virus* / immunology
  • Humans
  • Immunoglobulins / therapeutic use
  • Immunohistochemistry
  • Lamivudine / therapeutic use
  • Liver Cirrhosis / drug therapy
  • Liver Cirrhosis / surgery
  • Liver Cirrhosis / virology*
  • Liver Neoplasms / drug therapy
  • Liver Neoplasms / surgery
  • Liver Neoplasms / virology*
  • Liver Transplantation*
  • Male
  • Middle Aged
  • Organophosphonates / therapeutic use
  • Polymerase Chain Reaction
  • Risk Assessment
  • Risk Factors
  • Secondary Prevention
  • Sequence Analysis, DNA
  • Time Factors
  • Treatment Outcome
  • Viral Load
  • Virus Replication

Substances

  • Antiviral Agents
  • DNA, Circular
  • DNA, Viral
  • Hepatitis B Surface Antigens
  • Immunoglobulins
  • Organophosphonates
  • Lamivudine
  • adefovir
  • Adenine
  • hepatitis B hyperimmune globulin