Korean J Hepatol.
1999 Mar;5(1):12-21.
Long-erm Follow-p of Patients Treated with Interferon Alfa for Chronic Hepatitis B
Abstract
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BACKGROUND/AIMS: Several randomized controlled studies have shown that responders
who had treated with interferon alpha for chronic hepatitis B had better rate of sustained
loss of HBeAg and HBV DNA than non-esponders. These studies also showed that non-esponders
had higher rates of liver related complication and mortality. But there is very little data
on how well sustained responders are and whether the responders eventually lose HBsAg in Korea.
The aims of this study were to better define the long term remission of chronic hepatitis
B induced by interferon alfa therapy and compare the clinical outcome among the interferon
responders and non-esponders in Korea.
METHODS
Sixty-ight patients with chronic hepatitis
B who were treated with interferon alfa between 1987 and 1998 were followed up for serologic
status (HBsAg, HBeAg, HBV DNA), biochemical tests and liver related complication or mortality.
RESULTS
Among 68 patients with chronic hepatitis B who were treated with interferon alfa,
28 (41%) responded to treatment with loss of HBeAg within 1 year of starting treatment.
Up to 129 months (mean 58 months) after therapy, responders had higher rate of cumulative
clearance of HBeAg at five years than non-esponders (100% vs 35.1%, p<0.05).
Responders had maintained the normal serum ALT than nonresponders at five years (94% vs 55.6%, p<0.05).
Loss of HBsAg was not different between responders and non-esponders (5% vs 4%, NS).
The rates of liver related complication and mortality did not differ between both groups.
Delayed clearance of HBeAg occured in twelve out of forty non-esponders (30%).
There were no differences in age, baseline ALT, histologic finding of liver biopsy,
HBV DNA at the end of first year after study with IFN therapy between the non-esponders
with and without delayed clearance of HBeAg.
CONCLUSION
Remission in chronic hepatitis B induced by alfa interferon maintained
in long duration. But clinical outcomes such as liver related complication, mortality
and the elimination of HBV infection have no differences between responders and non-esponders.
Further studies are needed for the role of interferon therapy in long-erm clinical outcome
for chronic hepatitis B.