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首页> 外文期刊>Hepatology research: the official journal of the Japan Society of Hepatology >A multicenter survey of re-treatment with pegylated interferon plus ribavirin combination therapy for patients with chronic hepatitis C in Japan
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A multicenter survey of re-treatment with pegylated interferon plus ribavirin combination therapy for patients with chronic hepatitis C in Japan

机译:聚乙二醇干扰素联合利巴韦林联合治疗对日本慢性丙型肝炎患者的多中心调查

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Aim: This study aimed to clarify the factors associated the efficacy of re-treatment with pegylated interferon (PEG IFN) plus ribavirin combination therapy for patients with chronic hepatitis C who had failed to respond to previous treatment. Methods: One hundred and forty-three patients who had previously shown relapse (n=79), non-response (n=34) or intolerance (n=30) to PEG IFN plus ribavirin were re-treated with PEG IFN plus ribavirin. Results: Twenty-five patients with intolerance to previous treatment completed re-treatment and the sustained virological response (SVR) rates were 55% and 80% for hepatitis C virus (HCV) genotype 1 and 2, respectively. On re-treatment of the 113 patients who completed the previous treatment, the SVR rates were 48% and 63% for genotype 1 and 2, respectively. Relapse after previous treatment and a low baseline HCV RNA level on re-treatment were associated with SVR in genotype 1 (P<0.001). Patients with the interleukin-28B major genotype responded significantly better and earlier to re-treatment, but the difference in the SVR rate did not reach a significant level between the major and minor genotypes (P=0.09). Extended treatment of 72weeks raised the SVR rate among the patients who attained complete early virological response but not rapid virological response with re-treatment (72weeks, 73%, 16/22, vs 48weeks, 38%, 5/13, P<0.05). Conclusion: Relapse after previous treatment and a low baseline HCV RNA level have predictive values for a favorable response of PEG IFN plus ribavirin re-treatment for HCV genotype 1 patients. Re-treatment for 72weeks may lead to clinical improvement for genotype 1 patients with complete early virological response and without rapid virological response on re-treatment.
机译:目的:本研究旨在阐明与聚乙二醇化干扰素(PEG IFN)联合利巴韦林联合治疗对慢性丙型肝炎患者无效的重新治疗的疗效相关因素。方法:对先前显示复发(n = 79),无反应(n = 34)或不耐受(n = 30)对PEG IFN加利巴韦林的患者(343例)进行PEG IFN加利巴韦林治疗。结果:25名对先前治疗不耐受的患者完成了再次治疗,并且丙型肝炎病毒(HCV)基因型1和2的持续病毒学应答(SVR)率分别为55%和80%。在对完成先前治疗的113位患者进行重新治疗后,基因型1和2的SVR率分别为48%和63%。先前治疗后的复发和再次治疗后基线HCV RNA水平低与基因型1的SVR相关(P <0.001)。白细胞介素28B主要基因型的患者对再治疗的反应明显更好,更早,但主要和次要基因型之间的SVR率差异未达到显着水平(P = 0.09)。接受完全治疗的患者在接受完全早期病毒学应答但没有快速病毒学应答的情况下,72周的延长治疗提高了SVR率(72周,73%,16/22,而48周,38%,5/13,P <0.05) 。结论:先前治疗后的复发和低水平的HCV RNA水平对于PEG IFN联合利巴韦林再治疗对HCV基因型1患者具有良好的预测价值。再治疗72周可能会导致基因型1患者的临床改善,这些患者具有完全的早期病毒学应答并且在再次治疗时没有快速的病毒学应答。

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