Predictive Factors and Clinical Outcome of Viral Breakthrough during Lamivudine Treatment for Chronic Hepatitis B Infection |
Park Neunghwa , Sin Jeongu , Park Jongho , Bang Seongjo , Kim Daehyeon , Ju Gwanglo , Kim Doha |
Department of Internal Medicine, Ulsan University College of Medicine, Ulsan University Hospital, Ulsan, Korea |
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ABSTRACT |
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Background/Aims Long-term treatment with lamivudine causes breakthrough, but the clinical course
after lamivudine breakthrough is not well known. The aims of this study were to evaluate the clinical course
in lamivudine after breakthrough, and to identify predictive factors of breakthrough. Methods: 124 patients
with chronic hepatitis B infection, who represented viral breakthrough during lamivudine therapy, were
included. The mean duration of lamivudine therapy and additional lamivudine therapy after breakthrough was
30.5 months and 12.5 months, respectively. Results: The cumulative breakthrough rates at 12, 18, 24 and 36
months were 8, 24, 36 and 52%, respectively. After viral breakthrough, only 4 patients maintained normal ALT
levels. 120 patients showed ALT elevation. The number of patients with ALT levels greater than 5 times, and
greater than 10 times, the upper normal limit were 67 (56%) and 29 (24%), respectively. While still on
lamivudine therapy after breakthrough, 98 patients presented ALT elevation. Only 22 had normalized ALT
levels. Hepatic decompensation developed in 2 patients. HBeAg seroconversion after breakthrough occurred
in 10 patients. The changing pattern of quantitative HBeAg levels during lamivudine therapy was the only
predictive factor associated with viral breakthrough. The mean time of turning points in decrescendo-crescendo
patterns of HBeAg levels during lamivudine therapy was earlier than viral breakthrough (9 months vs. 17
months). Conclusions: These results suggested that deterioration of hepatic function can usually be observed
after breakthrough. The serial monitoring of serum quantitative HBeAg levels may allow an early recognition
of viral breakthrough.(Korean J Hepatol 2003;9:293-303) |
KeyWords:
Hepatitis/Viral/Chronic viral hepatitis B, Lamivudine, Viral breakthrough, HBeAg quantitation |
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