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对于丙型肝炎病毒6型慢性感染者,聚乙二醇干扰素联合利巴韦林治疗48周相比24周,持续病毒学应答率更高。

Higher rate of sustained virologic response in chronic hepatitis C genotype 6 treated with 48 weeks versus 24 weeks of peginterferon plus ribavirin.

作者信息

Nguyen Mindie H, Trinh Huy N, Garcia Ruel, Nguyen Gloria, Lam Khoa D, Keeffe Emmet B

机构信息

Division of Gastroenterology and Hepatology, Stanford University Medical Center, Palo Alto, California, USA.

出版信息

Am J Gastroenterol. 2008 May;103(5):1131-5. doi: 10.1111/j.1572-0241.2008.01793.x.

DOI:10.1111/j.1572-0241.2008.01793.x
PMID:18477343
Abstract

OBJECTIVES

Infection with hepatitis C virus (HCV) genotype 6 is common in patients from parts of China and Southeast Asia. No study to date has examined the treatment response to peginterferon and ribavirin (PEG IFN + RBV) in these patients, or the effects of treatment duration on sustained virologic response (SVR) rates.

METHODS

We performed a retrospective study of 190 consecutive Asian-American patients who were diagnosed with HCV genotype 6 at a gastroenterology clinic in northern California between 2001 and 2004, 66 of whom were treatment-naïve and subsequently completed 24 wk of IFN + RBV or PEG IFN + RBV or 48 wk of PEG IFN + RBV therapy. The primary outcome was SVR.

RESULTS

There was no statistical difference in SVR of 31 patients treated with 24 wk of IFN + RBV and in 23 patients treated with 24 wk of PEG IFN + RBV (51.6%vs 39%, P= 0.363). The SVR in 12 patients treated with 48 wk of PEG IFN + RBV was significantly higher than that in those treated for only 24 wk (75%vs 39%, P= 0.044).

CONCLUSIONS

Treatment-eligible patients with HCV genotype 6 should be treated with a full course of 48 wk as tolerated. Larger prospective studies of patients with HCV genotype 6 are needed to confirm the optimal treatment duration with PEG IFN + RBV.

摘要

目的

丙型肝炎病毒(HCV)6型感染在中国部分地区和东南亚患者中很常见。迄今为止,尚无研究考察这些患者接受聚乙二醇干扰素和利巴韦林(PEG IFN + RBV)治疗的反应,或治疗疗程对持续病毒学应答(SVR)率的影响。

方法

我们对2001年至2004年期间在加利福尼亚州北部一家胃肠病诊所被诊断为HCV 6型的190例连续的亚裔美国患者进行了一项回顾性研究,其中66例既往未接受过治疗,随后完成了24周的IFN + RBV或PEG IFN + RBV治疗或48周的PEG IFN + RBV治疗。主要结局为SVR。

结果

接受24周IFN + RBV治疗的31例患者与接受24周PEG IFN + RBV治疗的23例患者的SVR无统计学差异(51.6%对39%,P = 0.363)。接受48周PEG IFN + RBV治疗的12例患者的SVR显著高于仅接受24周治疗的患者(75%对39%,P = 0.044)。

结论

符合治疗条件的HCV 6型患者应在耐受的情况下接受48周的全程治疗。需要对HCV 6型患者进行更大规模的前瞻性研究,以确认PEG IFN + RBV的最佳治疗疗程。

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