Sustained Negativity for HCV-RNA over 24 or More Months by Long-Term Interferon Therapy Correlates with Eradication of HCV in Patients with Hepatitis C Virus Genotype 1b and High Viral Load

Sustained Negativity for HCV-RNA over 24 or More Months by Long-Term Interferon Therapy Correlates with Eradication of HCV in Patients with Hepatitis C Virus Genotype 1b and High Viral Load
复制标题

通过长期干扰素治疗,HCV-RNA 持续阴性超过 24 个月或更长,与丙型肝炎病毒基因型 1b 和高病毒载量患者的 HCV 根除相关

DOI:
--
复制
发表时间:
2004
期刊:
影响因子:
4.6
通讯作者:
H. Kumada
H. Kumada
中科院分区:
医学4区
文献类型:
--
作者:
Y. Arase;F. Suzuki;A. Tsubota;Yoshiyuki Suzuki;S. Saitoh;M. Kobayashi;N. Akuta;T. Someya;T. Hosaka;M. Kobayashi;H. Sezaki;K. Ikeda;H. Kumada

文献摘要

参考文献

被引文献

相似文献

目的:我们评估长期干扰素(IFN)治疗HCV- rna持续阴性超过24个月或更长时间是否与丙型肝炎病毒基因型1b和高病毒载量患者的HCV根除相关。方法:hcv - 1b基因型、病毒载量超过1 Meq/ml的患者每日给予6 MU天然IFN-α,持续2-8周,随后每周3次,持续16-22周,在IFN给药期间HCV-RNA阴性的患者403例。403例患者中有41例在初始IFN治疗后接受6 MU天然IFN-α治疗,每周3次,持续时间超过18个月(长期IFN组)。302例患者在6个月疗程结束后6个月内未接受任何IFN治疗(6个月IFN组)。持续病毒学反应(SVR)被定义为在IFN治疗完成后3个月和6个月的HCV-RNA阴性。结果:长期ifn组SVR为73.2%(30/41),6个月ifn组SVR为18.2%(55/302)。多因素分析显示,长期IFN治疗是SVR最显著的影响因素(p < 0.0001)。结论:基因型1b高病毒载量患者长期IFN治疗HCV-RNA持续阴性24个月及以上与SVR相关。
Objective: We assessed whether sustained negativity for HCV-RNA over 24 or more months by long-term interferon (IFN) therapy correlates with eradication of HCV in patients with hepatitis C virus genotype 1b and high viral load or not. Methods: The number of patients with HCV-genotype 1b and high viral load exceeding 1 Meq/ml who received 6 MU of natural IFN-α daily for 2–8 weeks, followed by three times/week for 16–22 weeks and negativity for HCV-RNA during IFN administration was 403. Forty-one of 403 patients received 6 MU of natural IFN-α three times/week for more than 18 months after the initial IFN therapy (long-term-IFN-group). Three hundred and two patients did not receive any IFN treatment for 6 months after the termination of the 6-month course (6-month-IFN-group). Sustained virological response (SVR) was defined as negative HCV-RNA at both 3 and 6 months after the completion of IFN therapy. Results: SVR was noted in 73.2% (30/41) of long-term-IFN-group and 18.2% (55/302) of 6-month-IFN-group. Multivariate analysis showed that long-term IFN therapy was the most significant contributor to SVR (p < 0.0001). Conclusion: Sustained negativity of HCV-RNA for 24 or more months by long-term IFN therapy correlated with SVR in patients with genotype 1b and high viral load.
DOI: 10.1056/nejm199811193392101
发表时间: 1998-11-19
影响因子: 158.5
作者:
McHutchison, JG;Gordon, SC;Albrecht, JK
通讯作者: Albrecht, JK