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Boceprevir in the treatment of hepatitis C infection: rationale and clinical data

机译:Boceprevir治疗丙型肝炎感染:基本原理和临床数据

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An estimated 1.8% of the population in the USA is infected with the hepatitis C virus (HCV). The standard of care treatment for HCV consists of peglFN and ribavirin. Genotype is considered a strong predictor determining response rates to treatment. Patients infected with genotype 1 are more resistant to treatment with an estimated response rate of approximately 40-50%. The recent discovery of polymorphisms in the IL28-B gene has given new insight into response rates and is now being considered the strongest pretreatment predictor of response. Recent insights into the HCV lifecycle and structure have led to the development of drugs that inhibit the NS3 protease in the HCV virus molecule, thereby preventing viral replication and increased degradation, and thus increasing chances of achieving a sustained viral response to therapy. Two drugs - boceprevir and telaprevir- have recently been approved by the US FDA and have been shown to have increased efficacy for genotype 1 patients, increasing the sustained virologic response rates to 75%. These drugs will be the biggest advance in the field since the introduction of peglFN and ribavirin.
机译:在美国,估计有1.8%的人口感染了丙型肝炎病毒(HCV)。 HCV的护理治疗标准包括peglFN和利巴韦林。基因型被认为是确定治疗反应率的有力预测指标。被基因型1感染的患者对治疗的抵抗力更高,估计的缓解率约为40-50%。 IL28-B基因多态性的最新发现为应答率提供了新的见识,现在被认为是最强的应答预处理指标。对HCV生命周期和结构的最新见解导致了抑制HCV病毒分子中NS3蛋白酶的药物的开发,从而阻止了病毒复制和增加的降解,从而增加了获得对治疗的持续病毒反应的机会。最近,两种药物-boceprevir和telaprevir-已获美国FDA批准,已显示对基因型1的患者具有更高的疗效,可将持续的病毒学应答率提高至75%。自引入peglFN和利巴韦林以来,这些药物将是该领域最大的进步。

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