首页> 外文期刊>Терапевтичесκий архив >Possibilities of using cepeginterferon alpha-2b in double (cepeginterferon alfa-2b and ribavirin) and triple (simeprevir, cepeginterferon alpha-2b, and ribavirin) antiviral therapy regimens for chronic hepatitis C. A review of clinical trials and experience of everyday clinical practice
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Possibilities of using cepeginterferon alpha-2b in double (cepeginterferon alfa-2b and ribavirin) and triple (simeprevir, cepeginterferon alpha-2b, and ribavirin) antiviral therapy regimens for chronic hepatitis C. A review of clinical trials and experience of everyday clinical practice

机译:在慢性丙型肝炎的双重(cepeginterferon alfa-2b和利巴韦林)和三次(simeprevir,cepeginterferonα-2b和利巴韦林)抗病毒治疗方案中使用cepeginterferon alpha-2b的可能性。临床试验的回顾和日常临床实践的经验

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Since the incidence of chronic hepatitis C (CHC) increases steadily, the priority of national health care is to provide antiviral therapy (AVT) for the maximum number of patients infected with hepatitis C virus (HCV). The regimens including pegylated interferons (PEG-IFN) are still in demand in the Russian Federation. A number of clinical trials have been conducted to evaluate the efficacy and safety of cepeginterferon alpha-2b (cePEG-IFN alpha-2b), an original PEG-IFN-α developed in the Russian Federation. Their results have shown that cePEG-IFN alpha-2b in the two-component AVT regimen has at least no less clinical efficacy than PEG-IFN alpha-2b and PEG-INF alpha-2a in HCV monoinfected and HCV/HIV co-infected patients. The pooled analysis of data has indicated that the use of cePEG-IFN alpha-b in combination with ribavirin allows an average of 80% of the patients with HCV genotypes 2 and 3 and 62% of those with HCV genotype 1 to achieve a sustained virological response (SVR). In clinical practice when the two-component AVT regimen (cePEG-IFN alpha-b and ribavirin) was used in patients with early-stage CHC and mild fibrosis, SVR was recorded in 90.7% of the patients with HCV genotype 2/3 and in 75% of those with HCV genotype 1. The experience in using cePEG-IFN alpha-2b as a component of the three-component AVT regimen (simeprevir, cePEG IFN alfa-2b, and ribavirin) has been published. The observational program manly covered young patients with mild or moderate fibrosis. SVR was observed in 94% of the patients. Another paper describes the experience with the triple AVT therapy (simeprevir, cePEG-IFN alfa-2b, and ribavirin) in 22 patients, the majority of whom had advanced fibrosis. SVR was recorded in 71.4% of those who hadcompleted treatment. Thus, an individual approach and assessment of predictive response factors to two- or three-component AVT regimens including cePEG-IFN alpha 2b can achieve successful treatment outcomes in most patients with CHC, which is, in some cases, more economically sound than interferon-free regimens used as first-line therapy.
机译:由于慢性丙型肝炎(CHC)的发病率稳步上升,因此国家卫生保健的重点是为感染丙型肝炎病毒(HCV)的最大患者提供抗病毒治疗(AVT)。俄罗斯联邦仍需要包括聚乙二醇化干扰素(PEG-IFN)在内的治疗方案。已经进行了许多临床试验,以评估cepeginterferon alpha-2b(cePEG-IFN alpha-2b)(俄罗斯联邦研制的原始PEG-IFN-α)的疗效和安全性。他们的研究结果表明,二组分AVT方案中的cePEG-IFN alpha-2b在HCV单感染和HCV / HIV合并感染患者中的临床疗效至少不低于PEG-IFN alpha-2b和PEG-INF alpha-2a。 。数据汇总分析表明,将cePEG-IFNα-b与利巴韦林联合使用可使HCV基因型2和3的患者平均占80%,而HCV基因型1的患者中平均占62%响应(SVR)。在临床实践中,在早期CHC合并轻度纤维化的患者中使用两成分AVT方案(cePEG-IFNα-b和利巴韦林)时,在90.7%的HCV基因型2/3和90%的患者中记录了SVR。 HCV基因型1的患者中有75%。已经公开了将cePEG-IFNα-2b用作三组分AVT方案(simeprevir,cePEG IFN alfa-2b和利巴韦林)的经验。观察计划主要覆盖了轻度或中度纤维化的年轻患者。 94%的患者观察到SVR。另一篇论文介绍了三例AVT治疗(simeprevir,cePEG-IFN alfa-2b和利巴韦林)的经验,其中22例患者大多数患有晚期纤维化。在完成治疗的患者中,有71.4%记录了SVR。因此,对于大多数CHC患者,单独的方法和对包括cePEG-IFNα2b在内的两组分或三组分AVT方案的预测反应因子的评估可以实现成功的治疗结果,在某些情况下,这种方法比干扰素治疗更经济免费方案用作一线治疗。

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