Lamivudine is an effective first-line therapy for chronic hepatitis B virus (HBV)
infection, accomplishing the goals of viral suppression, normalization of alanine
aminotransferase (ALT) levels, histological improvement, and seroconversion. In the
lamivudine clinical trials, up to 32% of patients positive for hepatitis B e antigen
(HBeAg) lost HBeAg after 1 year of treatment, and approximately 18% achieved HBeAg
seroconversion. ALT levels greater than five times the upper limit of normal increased
the likelihood of HBeAg loss. The rates of seroconversion and resistance both increase
with the length of treatment. In HBeAg-negative patients, two thirds showed response
after 6 to 12 months of therapy, but this response diminished over time despite continued
treatment, largely due to the emergence of resistance. Resistance is present in nearly
70% of patients at 5 years. Resistance reverses prior biochemical, virological, and
histological gains and can lead to progressive liver failure. Careful patient selection
is important, therefore, to maximize the potential for a treatment response under
limited therapy.
KEYWORDS
Lamivudine - resistance - hepatitis B - clinical trials
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Teresa L WrightM.D.
4150 Clement St, 111B
San Francisco, CA 94121
eMail: twright@itsa.ucsf.edu