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Peginterferon α-2b and ribavirin therapy in chronic hepatitis C genotype 4: impact of treatment duration and viral kinetics on sustained virological response

机译:聚乙二醇干扰素α-2b和利巴韦林治疗慢性丙型肝炎基因型4:治疗持续时间和病毒动力学对持续病毒学应答的影响

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摘要

>Background: The response rates and duration of peginterferon alpha (PEG-IFN-α) and ribavirin combination therapy in chronic hepatitis C genotype 4, the prevalent genotype in the Middle East and Africa, are poorly documented.>Aims: To compare the efficacy and safety of 24, 36, or 48 weeks of PEG-IFN-α-2b and ribavirin therapy in chronic hepatitis C genotype 4.>Methods: In this prospective, randomised, double blind study, 287 patients with chronic hepatitis C genotype 4 were randomly assigned to PEG-IFN-α-2b (1.5 μg/kg) once weekly plus daily ribavirin (1000–1200 mg) for 24 weeks (group A, n = 95), 36 weeks (group B, n = 96), or 48 weeks (group C, n = 96) and followed for 48 weeks after completion of treatment. Early viral kinetics and histopathological evaluation of pre- and post treatment liver biopsies were performed. The primary end point was viral clearance 48 weeks after completion of treatment.>Results: Sustained virological response was achieved in 29%, 66%, and 69% of patients treated with PEG-IFN-α-2b and ribavirin for 24, 36, and 48 weeks, respectively, by intention to treat analysis. No statistically significant difference in sustained virological response rates was detected between 36 and 48 weeks of therapy (p = 0.3). Subjects with sustained virological response showed greater antiviral efficacy (ɛ) and rapid viral load decline from baseline to treatment week 4 compared with non-responders and improvement in liver histology. The incidence of adverse events was higher in the group treated for 48 weeks.>Conclusion: PEG-IFN-α-2b and ribavirin for 36 or 48 weeks was more effective in the treatment of chronic hepatitis C genotype 4 than treatment for 24 weeks. Thirty six week therapy was well tolerated and produced sustained virological and histological response rates similar to the 48 week regimen.
机译:>背景:关于聚乙二醇干扰素α(PEG-IFN-α)和利巴韦林联合疗法在慢性丙型肝炎基因型4(中东和非洲流行的基因型)中的应答率和持续时间的文献报道很少。 strong>目的:比较PEG-IFN-α-2b和利巴韦林治疗24、36或48周对慢性丙型肝炎基因型4的疗效和安全性。>方法:这项前瞻性,随机,双盲研究将287例慢性丙型肝炎基因型4患者随机分配至每周一次,每天一次接受PEG-IFN-α-2b(1.5μg/ kg)加利巴韦林(1000–1200 mg),持续24周(组) A,n = 95,36周(B组,n = 96)或48周(C组,n = 96),并在治疗完成后随访48周。进行了治疗前和治疗后肝活检的早期病毒动力学和组织病理学评估。主要终点是治疗完成后48周的病毒清除率。>结果:在接受PEG-IFN-α-2b和PEG-IFN-α-2b治疗的患者中,分别有29%,66%和69%的患者获得了持续的病毒学应答利巴韦林分别打算治疗24、36和48周。在治疗的36至48周之间,未检测到持续病毒学应答率的统计学差异(p(=(0.3)。与无反应者相比,具有持续病毒学反应的受试者从基线到治疗第4周显示出更高的抗病毒功效(ɛ)和快速病毒载量下降,肝脏组织学得到改善。 48周治疗组不良事件发生率较高。>结论:PEG-IFN-α-2b和利巴韦林治疗36或48周对慢性丙型肝炎基因型4更有效。比治疗24周。 36周的治疗耐受性良好,并产生与48周方案相似的持续病毒学和组织学应答率。

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