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The Efficacy and Safety of Peginterferon-alpha-2a in Korean Patients with Chronic Hepatitis B: A Multicenter Study Conducted in a Real Clinical Setting

Authors
Kwon, Jung HyunKim, Young SeokKim, Sang GyuneJang, Jeong WonKim, Tae HunJung, Young KulKwon, Oh Sang
Issue Date
Mar-2013
Publisher
EDITORIAL OFFICE GUT & LIVER
Keywords
Peginterferon; Chronic hepatitis B; Asian continental ancestry group
Citation
GUT AND LIVER, v.7, no.2, pp.197 - 205
Journal Title
GUT AND LIVER
Volume
7
Number
2
Start Page
197
End Page
205
URI
https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/14684
DOI
10.5009/gnl.2013.7.2.197
ISSN
1976-2283
Abstract
Background/Aims: Genotype C is the principal type of hepatitis B virus (HBV) in Koreans and is associated with poor prognosis for peginterferon alpha-2a therapy. The efficacy of and compliance to peginterferon a-2a therapy were investigated in Koreans with hepatitis B in a real clinical setting. Methods: Hepatitis B patients treated with peginterferon alpha-2a from 2008 to 2011 at four university hospitals were consecutively enrolled. Results: Eighty-eight patients were enrolled; 67 were hepatitis B e antigen (HBeAg)-positive. The mean treatment period was 36.1 +/- 15.2 weeks. In 26.1% of patients, treatment was discontinued due to insufficient antiviral effects and adverse events. At 24 weeks after treatment, 10/42 (23.8%) HBeAg-positive patients achieved both III3V DNA suppression to <2,000 IU/mL and HBeAg loss/seroconversion. For HBeAg-negative patients, 10/13 (76.9%) achieved HBV DNA suppression to <2,000 IU/niL at 24 weeks after treatment. During the follow-up period, 15 (30.6%) of the 49 patients who achieved HBV DNA suppression to 2,000 IU/mL developed a breakthrough HBV DNA level of >2x10(6) IU/mL. Conclusions: Peginterferon alpha-2a therapy in Koreans with hepatitis B in a real clinical setting resulted in a lower virologic response, as compared to Western individuals, but a favorable durability. There is a need to reduce the high rate of premature discontinuation compared to the controlled studies. (Gut Liver 2013;7:197-205)
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