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慢性基因型 1 HCV 肝炎患者抗病毒治疗的结果。507 例患者的回顾性研究。

Outcome of antiviral treatment in patients with chronic genotype 1 HCV hepatitis. A retrospective study in 507 patients.

机构信息

Department of Gastroenterology and Hepatology, University of Medicine and Pharmacy, Timişoara, Romania.

出版信息

J Gastrointestin Liver Dis. 2010 Sep;19(3):261-4.

Abstract

BACKGROUND AND AIM

The current standard of care in chronic HCV genotype 1 hepatitis is the combination of pegylated interferon (PegIFN) with ribavirin for 48 weeks. The aim of our paper was to verify if there are significant differences regarding the sustained virologic response (SVR) in patients treated with PegIFN alfa-2a vs. those treated PegIFN alpha-2b, both in combination with ribavirin.

METHOD

We performed a retrospective study on 507 patients with chronic viral C hepatitis treated with PegIFN alpha-2a 180 microg/kg/week or PegIFN alpha-2b 1.5 microg/kg/week plus ribavirin in the recommended doses according to weight, following the current treatment guidelines. We evaluated the SVR defined as PCR RNA-HCV undetectable 24 weeks after the end of treatment.

RESULTS

There were no differences regarding the baseline characteristics among the subgroups of patients treated with PegIFN alpha-2a or PegIFN alpha-2b concerning the pretreatment viral load (p=0.2445), the severity of fibrosis (p=0.2403), the mean age of the patients (p=0.9597) and the women/men ratio (p=0.2087). The SVR rates in patients treated with PegIFN alpha-2a were similar to those in patients treated with PegIFN alpha-2b: 208/338 (61.5%) vs. 94/169 (55.6%) (p=0.2129).

CONCLUSION

Sustained virologic response rates were similar in HCV genotype 1 patients treated with PegIFN alpha-2a and with Peg-IFN alpha-2b.

摘要

背景与目的

慢性丙型肝炎基因型 1 患者的现行标准治疗方案是聚乙二醇干扰素(PegIFN)联合利巴韦林治疗 48 周。我们的目的是验证聚乙二醇干扰素 alfa-2a 与聚乙二醇干扰素 alfa-2b 联合利巴韦林治疗的患者在持续病毒学应答(SVR)方面是否存在显著差异。

方法

我们对 507 例慢性丙型肝炎病毒感染患者进行了回顾性研究,这些患者按照现行治疗指南,分别接受聚乙二醇干扰素 alfa-2a 180μg/kg/周或聚乙二醇干扰素 alfa-2b 1.5μg/kg/周联合利巴韦林治疗,利巴韦林的剂量根据体重确定。我们评估了 SVR,定义为治疗结束后 24 周时 PCR RNA-HCV 不可检测。

结果

接受聚乙二醇干扰素 alfa-2a 或聚乙二醇干扰素 alfa-2b 治疗的患者亚组之间,在基线特征方面无差异,包括治疗前病毒载量(p=0.2445)、纤维化严重程度(p=0.2403)、患者平均年龄(p=0.9597)和男女比例(p=0.2087)。接受聚乙二醇干扰素 alfa-2a 治疗的患者 SVR 率与接受聚乙二醇干扰素 alfa-2b 治疗的患者相似:208/338(61.5%)vs. 94/169(55.6%)(p=0.2129)。

结论

聚乙二醇干扰素 alfa-2a 和聚乙二醇干扰素 alfa-2b 治疗丙型肝炎基因型 1 患者的 SVR 率相似。

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