The benefit of
lamivudine (
LAM) in hepatitis B virus (HBV)
infection is compromised by the progressively increasing emergence of
drug-resistant mutant strains. Although the addition of
adefovir dipivoxil (ADV) usually induces complete suppression of viral replication, primary non-response to ADV in
LAM resistant patients has been reported in a variable percentage of cases. Here we report a case of a patient with HBV
infection and
hepatocellular carcinoma who started
LAM therapy and subsequently developed virological breakthrough. The patient was given ADV, but HBV-
DNA negativisation was not reached. However, HBV clearance was obtained when the patient was switched from ADV to
tenofovir. Virological evaluations showed two well-known
LAM-related mutations (rtL180M and rtM204I) in addition to
reverse-transcriptase rtQ215H. This is the first case suggesting that this mutation may have an impact on viral replication. Finally, we also report that rtQ215H is responsive to
tenofovir.