Lee Heon Ju, Eun Jong Ryul, Choi Jae Won, Kim Kyung Ok, Moon Hee Jung
Department of Internal Medicine, Yeungnam University College of Medicine, Daegu, Korea.
Korean J Hepatol. 2008 Mar;14(1):46-57. doi: 10.3350/kjhep.2008.14.1.46.
BACKGROUND/AIMS: This study compared the efficacy and safety of combined peginterferon alfa (PEG-IFN) and ribavirin with that of combined interferon alpha (IFN-alpha) and ribavirin, according to the treatment duration in Korean patients with chronic hepatitis C.
Medical records of 86 patients treated with PEG-IFN and ribavirin (mean age, 50.7 years; males/females, 57/29; genotypes 1/2, 59/27) and 134 patients treated with IFN-alpha and ribavirin (mean age, 50.9 years; males/females 74/60; genotypes 1/2, 79/55) were reviewed. Ribavirin was administered at doses of 600-1,200 mg and 600-800 mg in patients with genotypes 1 and 2, respectively.
Sustained virological responses (SVRs) were evident in 68.4% and 41.7% of genotype 1 patients treated for 48 weeks in the PEG-IFN and IFN-alpha groups, respectively (P=0.021), and in 94.1% and 64.9% of genotype 2 patients treated for 24 weeks (P=0.026). Some genotype 1 patients treated for 24 weeks in the PEG-IFN group, who all exhibited negative HCV PCR results at week 12, showed an SVR of 87.5% (7/8).
The rate of SVRs in Korean patients with chronic hepatitis C was higher for combined PEG-IFN and ribavirin than for combined IFN-alpha and ribavirin. Further study is needed to clarify the outcome of short-term therapy in patients with a rapid or early virological response.
背景/目的:本研究比较了聚乙二醇干扰素α(PEG-IFN)联合利巴韦林与干扰素α(IFN-α)联合利巴韦林治疗韩国慢性丙型肝炎患者的疗效和安全性,并根据治疗疗程进行分析。
回顾了86例接受PEG-IFN和利巴韦林治疗的患者(平均年龄50.7岁;男/女,57/29;基因1/2型,59/27)以及134例接受IFN-α和利巴韦林治疗的患者(平均年龄50.9岁;男/女,74/60;基因1/2型,79/55)的病历。基因1型和2型患者利巴韦林的给药剂量分别为600 - 1200 mg和600 - 800 mg。
在PEG-IFN组和IFN-α组中,接受48周治疗的基因1型患者的持续病毒学应答(SVR)率分别为68.4%和41.7%(P = 0.021);接受24周治疗的基因2型患者的SVR率分别为94.1%和64.9%(P = 0.026)。在PEG-IFN组中,部分接受24周治疗的基因1型患者在第12周时HCV PCR结果均为阴性,其SVR率为87.5%(7/8)。
韩国慢性丙型肝炎患者中,PEG-IFN联合利巴韦林治疗的SVR率高于IFN-α联合利巴韦林治疗。需要进一步研究以明确病毒学应答快速或早期患者短期治疗的结果。