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聚乙二醇干扰素α-2b联合利巴韦林治疗24周对基因1型感染且治疗前病毒血症水平较低的慢性丙型肝炎患者的疗效。

Efficacy of 24 weeks treatment with peginterferon alfa-2b plus ribavirin in patients with chronic hepatitis C infected with genotype 1 and low pretreatment viremia.

作者信息

Zeuzem Stefan, Buti Maria, Ferenci Peter, Sperl Jan, Horsmans Yves, Cianciara Janusz, Ibranyi Endre, Weiland Ola, Noviello Stephanie, Brass Clifford, Albrecht Janice

机构信息

Clinic of Internal Medicine II, Department of Medicine, Saarland University Hospital, Kirrbergerstrasse, 66421 Homburg/Saar, Germany.

出版信息

J Hepatol. 2006 Jan;44(1):97-103. doi: 10.1016/j.jhep.2005.10.003. Epub 2005 Nov 7.

Abstract

BACKGROUND/AIMS: Previous studies using standard interferon and ribavirin combination therapy suggested that patients infected with HCV-1 and a low pretreatment HCV-RNA level can be treated for 24 weeks without compromising sustained virologic response rates. The aim of the present study was to investigate this schedule in the era of pegylated interferon-alpha plus ribavirin.

METHODS

Patients chronically infected with HCV-1 (n=235) and a screening viremia < or =600,000 IU/mL (real-time PCR) were treated with peginterferon alfa-2b 1.5 microg/kg subcutaneously once weekly plus ribavirin 800-1400 mg/day based on body weight for 24 weeks.

RESULTS

End-of-treatment and sustained virologic response rates were 80 and 50%, respectively. The 48-week historical control (Manns et al., Lancet 2001;358:958-65) had similar end-of-treatment (74%) but higher sustained virologic response rates (71%). This difference was due to a high virologic relapse rate after 24 weeks of therapy (37%) compared with the historical control (4%). A subset of patients who had undetectable serum HCV-RNA at treatment week 4, however, achieved similar sustained virologic response rate (89%) as in the control group (85%).

CONCLUSIONS

HCV-1 infected patients with a low baseline HCV-RNA concentration who become HCV-RNA negative at week 4 may be treated for 24 weeks without compromising sustained virologic response rates.

摘要

背景/目的:既往使用标准干扰素和利巴韦林联合治疗的研究表明,感染丙型肝炎病毒1型(HCV-1)且治疗前HCV-RNA水平较低的患者可接受24周治疗,而不影响持续病毒学应答率。本研究的目的是在聚乙二醇化干扰素-α加利巴韦林时代研究这一治疗方案。

方法

对235例慢性感染HCV-1且筛查病毒血症≤600,000 IU/mL(实时PCR法)的患者,皮下注射聚乙二醇化干扰素α-2b 1.5 μg/kg,每周1次,同时根据体重给予利巴韦林800 - 1400 mg/天,治疗24周。

结果

治疗结束时应答率和持续病毒学应答率分别为80%和50%。48周的历史对照(Manns等人,《柳叶刀》2001年;358:958 - 65)治疗结束时应答率相似(74%),但持续病毒学应答率更高(71%)。这种差异是由于治疗24周后病毒学复发率较高(37%),而历史对照为4%。然而,在治疗第4周血清HCV-RNA检测不到的一部分患者,其持续病毒学应答率与对照组相似(89%对85%)。

结论

HCV-1感染且基线HCV-RNA浓度较低、在第4周时HCV-RNA转阴的患者,可接受24周治疗而不影响持续病毒学应答率。

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