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Treating HCV Infection: It Doesn't Get Much Better Than This.治疗丙型肝炎病毒感染:没有比这更好的了。
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2
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No impact of resistance-associated substitutions on the efficacy of sofosbuvir, velpatasvir, and voxilaprevir for 12 weeks in HCV DAA-experienced patients.在 DAA 经治的 HCV 患者中,12 周内无耐药相关替换对索磷布韦、维帕他韦和沃维沙韦疗效的影响。
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Real-life effectiveness and safety of sofosbuvir/velpatasvir/voxilaprevir in hepatitis C patients with previous DAA failure.索磷布韦/维帕他韦/伏西瑞韦治疗既往 DAA 失败的丙型肝炎患者的真实世界疗效和安全性。
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Real-world effectiveness of sofosbuvir/velpatasvir/voxilaprevir in 573 direct-acting antiviral experienced hepatitis C patients.573 例直接作用抗病毒药物经验的丙型肝炎患者中索磷布韦/维帕他韦/沃诺拉韦的真实世界疗效。
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Cost-effectiveness of pan-genotypic direct-acting antiviral regimens for treatment of chronic Hepatitis C in the United States.泛基因型直接作用抗病毒治疗方案治疗美国慢性丙型肝炎的成本效益。
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引用本文的文献

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Sofosbuvir/velpatasvir in treatment-experienced HCV-infected patients - short report.索磷布韦/维帕他韦用于经治丙型肝炎病毒感染患者——简短报告
Clin Exp Hepatol. 2020 Feb;6(1):60-62. doi: 10.5114/ceh.2020.93059. Epub 2020 Feb 17.

本文引用的文献

1
Efficacy and Pharmacokinetics of Glecaprevir and Pibrentasvir With Concurrent Use of Acid-Reducing Agents in Patients With Chronic HCV Infection.在慢性 HCV 感染患者中,使用雷迪帕韦和奥比帕利联合应用酸抑制剂的疗效和药代动力学。
Clin Gastroenterol Hepatol. 2019 Feb;17(3):527-535.e6. doi: 10.1016/j.cgh.2018.07.003. Epub 2018 Sep 10.
2
Glecaprevir-Pibrentasvir for 8 or 12 Weeks in HCV Genotype 1 or 3 Infection.格卡瑞韦哌仑他韦片治疗 8 或 12 周用于治疗 1 型或 3 型丙型肝炎病毒感染。
N Engl J Med. 2018 Jan 25;378(4):354-369. doi: 10.1056/NEJMoa1702417.
3
Glecaprevir/Pibrentasvir in patients with hepatitis C virus genotype 1 or 4 and past direct-acting antiviral treatment failure.格卡瑞韦/哌仑他韦在既往直接作用抗病毒药物治疗失败的丙型肝炎病毒 1 型或 4 型患者中的应用。
Hepatology. 2018 Apr;67(4):1253-1260. doi: 10.1002/hep.29671. Epub 2018 Jan 30.
4
Glecaprevir and Pibrentasvir in Patients with HCV and Severe Renal Impairment.格卡瑞韦和哌仑他韦治疗丙型肝炎病毒合并严重肾功能损害患者。
N Engl J Med. 2017 Oct 12;377(15):1448-1455. doi: 10.1056/NEJMoa1704053.
5
Glecaprevir/pibrentasvir for hepatitis C virus genotype 3 patients with cirrhosis and/or prior treatment experience: A partially randomized phase 3 clinical trial.格卡瑞韦/哌仑他韦治疗伴有肝硬化和/或既往治疗史的丙型肝炎病毒基因型 3 患者:一项部分随机 3 期临床试验。
Hepatology. 2018 Feb;67(2):514-523. doi: 10.1002/hep.29541. Epub 2018 Jan 4.
6
Sofosbuvir, Velpatasvir, and Voxilaprevir for Previously Treated HCV Infection.索磷布韦、维帕他韦和沃西拉韦治疗既往 HCV 感染。
N Engl J Med. 2017 Jun 1;376(22):2134-2146. doi: 10.1056/NEJMoa1613512.
7
Efficacy of 8 Weeks of Sofosbuvir, Velpatasvir, and Voxilaprevir in Patients With Chronic HCV Infection: 2 Phase 3 Randomized Trials.索磷布韦、维帕他韦和沃士韦三者联用治疗慢性丙型肝炎病毒感染患者 8 周的疗效:两项 3 期随机试验。
Gastroenterology. 2017 Jul;153(1):113-122. doi: 10.1053/j.gastro.2017.03.047. Epub 2017 Apr 5.
8
Glecaprevir and pibrentasvir for 12 weeks for hepatitis C virus genotype 1 infection and prior direct-acting antiviral treatment.glecaprevir和pibrentasvir治疗丙型肝炎病毒1型感染及既往直接抗病毒治疗12周。
Hepatology. 2017 Aug;66(2):389-397. doi: 10.1002/hep.29081. Epub 2017 Apr 10.
9
Hepatitis C virus directly acting antivirals: current developments with NS3/4A HCV serine protease inhibitors.丙型肝炎病毒直接作用抗病毒药物:NS3/4A 丙型肝炎病毒丝氨酸蛋白酶抑制剂的最新进展。
J Antimicrob Chemother. 2010 Oct;65(10):2063-9. doi: 10.1093/jac/dkq284. Epub 2010 Aug 4.

治疗丙型肝炎病毒感染:没有比这更好的了。

Treating HCV Infection: It Doesn't Get Much Better Than This.

作者信息

Naggie Susanna

机构信息

Duke University School of Medicine, Druham, NC, USA.

出版信息

Top Antivir Med. 2019 Jan;26(4):104-108.

PMID:30641483
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6372361/
Abstract

Direct-acting antiviral (DAA) regimens now allow treatment of previously untreated or treated (including prior DAA failures) patients with chronic hepatitis C virus (HCV) infection with 8 or 12 week regimens, largely without the use of ribavirin. Newer next-generation pan-genotypic regimens with activity against resistance-associated substitutions include glecaprevir/pibrentasvir (GLE/PIB), a combination of a nonstructural protein (NS)3 protease inhibitor and an NS5A inhibitor, and sofosbuvir/velpatasvir/voxilaprevir (SOF/VEL/VOX), a combination of an NS5B polymerase inhibitor, NS5A inhibitor, and NS3 protease inhibitor. Both regimens have indications in DAA-experienced patients. GLE/PIB is approved for treatment of patients with genotype 1, 2, 3, 4, 5, or 6 infection without cirrhosis or with compensated cirrhosis and for the treatment of patients with genotype 1 infection previously treated with a regimen containing an NS5A inhibitor or an NS3/4A protease inhibitor, but not the combination. SOF/VEL/VOX is approved for retreatment of patients without cirrhosis or with compensated cirrhosis with genotype 1, 2, 3, 4, 5, or 6 infection previously treated with an NS5A inhibitor-containing regimen, or with genotype 1a or 3 previously treated with a SOF-containing regimen without an NS5A inhibitor. This article summarizes an IAS-USA webinar given by Susanna Naggie, MD, MHS, on August 30, 2018.

摘要

直接抗病毒(DAA)方案现可用于治疗既往未接受过治疗或接受过治疗(包括既往DAA治疗失败)的慢性丙型肝炎病毒(HCV)感染患者,疗程为8周或12周,且大多无需使用利巴韦林。具有抗耐药相关替代活性的新一代泛基因型方案包括glecaprevir/pibrentasvir(GLE/PIB),它是一种非结构蛋白(NS)3蛋白酶抑制剂与NS5A抑制剂的组合;还有sofosbuvir/velpatasvir/voxilaprevir(SOF/VEL/VOX),它是一种NS5B聚合酶抑制剂、NS5A抑制剂与NS3蛋白酶抑制剂的组合。这两种方案都适用于有DAA治疗经验的患者。GLE/PIB被批准用于治疗基因型1、2、3、4、5或6感染且无肝硬化或代偿性肝硬化的患者,以及用于治疗既往接受过含NS5A抑制剂或NS3/4A蛋白酶抑制剂(但不是二者联合)方案治疗的基因型1感染患者。SOF/VEL/VOX被批准用于对无肝硬化或代偿性肝硬化且基因型1、2、3、4、5或6感染的患者进行再治疗,这些患者既往接受过含NS5A抑制剂方案的治疗,或基因型1a或3既往接受过不含NS5A抑制剂的含sofosbuvir方案的治疗。本文总结了2018年8月30日由医学博士、医学硕士苏珊娜·纳吉举办的IAS-美国网络研讨会的内容。