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Changing the face of hepatitis C management – the design and development of sofosbuvir

机译:改变丙型肝炎管理的面貌–索非布韦的设计和开发

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Abstract: The availability of direct-acting antiviral (DAA) therapy has launched a new era in the management of chronic hepatitis C. Sofosbuvir, a uridine nucleotide analog that inhibits the hepatitis C RNA-dependent RNA polymerase, is the backbone of chronic hepatitis C therapy. Acting at the catalytic site of the polymerase, sofosbuvir is highly potent in suppressing viral replication and has a high genetic barrier to resistance. Sofosbuvir is effective across all hepatitis C genotypes, and is a mainstay of interferon-free combination therapy. In Phase II and III studies, genotype 1 patients who took sofosbuvir in combination with another DAA such as the NS3-4A protease inhibitor, simeprevir, or the NS5A replication complex inhibitors, ledipasvir or daclatasvir, achieved a sustained virologic response rate of over 90%. Harvoni?, a combination tablet of sofosbuvir and ledipasvir, dosed once daily is recommended for 24?weeks for treatment-experienced genotype 1 patients with cirrhosis, but 12?weeks of therapy is sufficient for all other populations. While genotype 2 (12?weeks or 16?weeks) and treatment-na?ve genotype 3 patients (24?weeks) have excellent response rates with sofosbuvir and ribavirin, treatment-experienced cirrhotic genotype 3 patients may need the addition of another DAA such as daclatasvir. Sofosbuvir is efficacious in special populations such as HIV–hepatitis C virus-coinfected patients and liver transplant recipients and has already made a profound impact in these groups. Since it is renally eliminated, patients with advanced kidney disease or on dialysis must await dosing recommendations. Sofosbuvir-based regimens appear to be well tolerated with headache and fatigue being the most common side effects. The opportunity to cure patients with hepatitis C with sofosbuvir combination therapy is likely to change the future for our patients, particularly if the emphasis shifts to identifying those patients unaware that they are infected and providing affordable access to treatment.
机译:摘要:直接作用抗病毒(DAA)治疗的可用性开创了慢性丙型肝炎治疗的新纪元。索福布韦是一种抑制丙型肝炎RNA依赖性RNA聚合酶的尿苷核苷酸类似物,是慢性丙型肝炎的骨干。治疗。索福布韦在聚合酶的催化位点起作用,在抑制病毒复制方面非常有效,并且对耐药性具有很高的遗传屏障。 Sofosbuvir对所有丙型肝炎基因型均有效,并且是无干扰素联合疗法的支柱。在II期和III期研究中,将sofosbuvir与另一种DAA(例如NS3-4A蛋白酶抑制剂,simeprevir或NS5A复制复合物抑制剂,ledipasvir或daclatasvir)联合使用的基因型1患者实现了超过90%的持续病毒学应答率。对于有治疗经验的基因型1型肝硬化患者,建议每天服用一次Sovosbuvir和ledipasvir的组合片剂Harvoni?24?周,但对于所有其他人群而言,治疗12?周就足够了。尽管基因型2(12周或16周)和未经治疗的基因3型患者(24周)对索非布韦和利巴韦林的应答率极高,但有治疗经验的肝硬化基因3型患者可能需要另外加用DAA,例如作为达卡他韦。 Sofosbuvir在特殊人群(例如感染HIV-C型肝炎病毒的患者和肝移植受者)中有效,并且已经在这些人群中产生了深远的影响。由于已被肾脏淘汰,患有晚期肾脏疾病或接受透析的患者必须等待给药建议。基于Sofosbuvir的治疗方案似乎可以很好地耐受,头痛和疲劳是最常见的副作用。用sofosbuvir联合疗法治愈丙型肝炎患者的机会可能会改变我们患者的未来,尤其是如果重点已转移到识别那些不知道自己被感染的患者并提供负担得起的治疗机会时。

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