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聚乙二醇干扰素联合利巴韦林再治疗方案对日本慢性丙型肝炎患者的疗效。

Efficacy of re-treatment with pegylated interferon plus ribavirin combination therapy for patients with chronic hepatitis C in Japan.

机构信息

Department of Gastroenterology and Hepatology, Osaka University Graduate School of Medicine, Yamadaoka, Suita, Japan.

出版信息

J Gastroenterol. 2011 Aug;46(8):1031-7. doi: 10.1007/s00535-011-0409-7. Epub 2011 May 3.

Abstract

BACKGROUND

It is still not known which patients with chronic hepatitis C who failed to respond to previous pegylated interferon (Peg-IFN) plus ribavirin therapy can benefit from re-treatment.

METHODS

Seventy-four patients (HCV genotype 1, n = 56, genotype 2, n = 18) were re-treated with Peg-IFN plus ribavirin.

RESULTS

On re-treatment, the sustained virologic response (SVR) rate was 41% for genotype 1 and 56% for genotype 2. With genotype 1, the factors associated with an SVR were previous treatment response and the serum hepatitis C virus (HCV) RNA level at the start of re-treatment. Patients with a ≥ 2-log decrease in HCV RNA at week 12 (partial early virologic response, p-EVR) in previous treatment had significantly higher SVR rates than those without these decreases (p < 0.001); no patient without a p-EVR in the previous treatment attained an SVR with re-treatment (0/16). All patients with <5 log(10) IU/ml of HCV RNA at the start of re-treatment attained an SVR (6/6), while only 33% (15/45) of those patients with ≥ 5 log(10) IU/ml of HCV RNA attained an SVR (p < 0.01). Among the patients with relapse in the previous treatment, those who attained an SVR on re-treatment required a longer duration of re-treatment than the duration of the previous treatment (re-treatment, 63.8 ± 13.0 weeks vs. previous treatment, 53.9 ± 13.5 weeks, p = 0.01).

CONCLUSIONS

Re-treatment of genotype 1 patients should be limited to patients with a p-EVR in the previous treatment and a low HCV RNA level at the start of re-treatment. In re-treatment with Peg-IFN plus ribavirin, longer treatment duration can contribute to increasing the anti-viral effect.

摘要

背景

目前尚不清楚先前接受聚乙二醇干扰素(Peg-IFN)联合利巴韦林治疗无应答的慢性丙型肝炎患者中,哪些患者可以从中获益于再治疗。

方法

74 例患者(HCV 基因型 1,n=56;基因型 2,n=18)接受 Peg-IFN 联合利巴韦林再治疗。

结果

再治疗时,基因型 1 的持续病毒学应答(SVR)率为 41%,基因型 2 的 SVR 率为 56%。对于基因型 1,与 SVR 相关的因素包括先前的治疗反应和再治疗开始时血清丙型肝炎病毒(HCV)RNA 水平。先前治疗中第 12 周 HCV RNA 下降≥2log(部分早期病毒学应答,p-EVR)的患者 SVR 率显著高于未下降的患者(p<0.001);先前治疗中无 p-EVR 的患者无一例再治疗获得 SVR(0/16)。所有再治疗开始时 HCV RNA<5log(10)IU/ml 的患者均获得 SVR(6/6),而 HCV RNA≥5log(10)IU/ml 的患者中仅 33%(15/45)获得 SVR(p<0.01)。在先前治疗中复发的患者中,再治疗获得 SVR 的患者再治疗时间长于先前治疗时间(再治疗,63.8±13.0 周 vs. 先前治疗,53.9±13.5 周,p=0.01)。

结论

基因型 1 患者的再治疗应仅限于先前治疗中具有 p-EVR 和再治疗开始时 HCV RNA 水平较低的患者。在 Peg-IFN 联合利巴韦林再治疗中,延长治疗时间有助于增强抗病毒效果。

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