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Multicenter comparison of PEG-IFN alpha 2a or alpha 2b plus ribavirin for treatment-naive HCV patient in Korean population

Authors
Jin, Young-JooLee, Jin-WooLee, Jung IlPark, Sang HoonPark, Choong KeeKim, Young SeokJeong, Sook-HyangKim, Yun SooKim, Ju HyunHwang, Seong GyuRim, Kyu SungYim, Hyung JoonCheong, Jae YounCho, Sung WonLee, June SungPark, Young MinJang, Jeong WonLee, Chun KyonSohn, Joo HyunYang, Jin MoHan, Seungbong
Issue Date
Apr-2013
Publisher
BIOMED CENTRAL LTD
Keywords
Chronic hepatitis C; Pegylated interferon alfa-2a; Pegylated interferon alfa-2b; Ribavirin; Sustained virological response
Citation
BMC GASTROENTEROLOGY, v.13
Journal Title
BMC GASTROENTEROLOGY
Volume
13
URI
https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/14671
DOI
10.1186/1471-230X-13-74
ISSN
1471-230X
Abstract
Background: Two recent Italian studies suggested that Pegylated-interferon (PEG-IFN) alfa-2a achieves a higher sustained virological response (SVR) rate than PEG-IFN alfa-2b. We intended to compare the efficacy and safety of PEG-IFN alfa-2a with those of PEG-IFN alfa-2b in Korean patients with chronic hepatitis C virus (HCV). Methods: This retrospective, multi-center trial was conducted on 661 treatment-naive chronic HCV patients. Patients received PEG-IFN alfa-2a (180 mu g/week; n=402) or PEG-IFN alfa-2b (1.5 mu g/kg/week; n=259) with ribavirin (800-1200 mg/day) for 24 or 48 weeks according to HCV genotypes. Results: Early virologic response and sustained virologic response (SVR) rates were not significantly different between two PEG-IFN groups both in patients with HCV genotype 1 (all P-values>0.05) and 2/3 (all P-values>0.05). SVR rates were not different between two groups in each categorized baseline characteristics: age (years) (<= 50 and >50), HCV viral load (IU/mL) (<= 7x10(5) and >7x10(5)), and hepatic fibrosis (F0-2 and F3-4) (all P-values >0.05). In additional analysis for 480 patients who sufficiently complied with treatment doses and duration (80/80/80 rule) and propensity-score matched analysis, SVR rates were not different between two groups both in patients with HCV genotype 1 and 2/3 (all P-values >0.05). Adverse event rates were similar between two groups. Conclusions: Unlike the Western data, efficacy and safety of PEG-IFN alfa-2a were similar to those of PEG-IFN alfa-2b in chronically HCV-infected Korean patients regardless of age, HCV viral load, and hepatic fibrosis.
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