• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

在使用帕利哌韦-利托那韦、奥比他韦和达沙布韦的AVIATOR研究中,丙型肝炎病毒1型基线和治疗中出现的变异的耐药性分析。

Resistance analysis of baseline and treatment-emergent variants in hepatitis C virus genotype 1 in the AVIATOR study with paritaprevir-ritonavir, ombitasvir, and dasabuvir.

作者信息

Krishnan Preethi, Tripathi Rakesh, Schnell Gretja, Reisch Thomas, Beyer Jill, Irvin Michelle, Xie Wangang, Larsen Lois, Cohen Daniel, Podsadecki Thomas, Pilot-Matias Tami, Collins Christine

机构信息

Research and Development, AbbVie Inc., North Chicago, Illinois, USA

Research and Development, AbbVie Inc., North Chicago, Illinois, USA.

出版信息

Antimicrob Agents Chemother. 2015 Sep;59(9):5445-54. doi: 10.1128/AAC.00998-15. Epub 2015 Jun 22.

DOI:10.1128/AAC.00998-15
PMID:26100711
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4538512/
Abstract

AVIATOR, a phase 2 clinical trial, evaluated ritonavir-boosted paritaprevir (a protease inhibitor), ombitasvir (an NS5A inhibitor), and dasabuvir (a nonnucleoside polymerase inhibitor) (the three-drug [3D] regimen) with or without ribavirin (RBV) for 8, 12, or 24 weeks in 406 HCV genotype 1 (GT1)-infected patients. The rate of sustained virologic response 24 weeks after treatment ranged from 88% to 100% across the arms of the 3D regimen with or without RBV; 20 GT1a-infected patients and 1 GT1b-infected patient experienced virologic failure (5.2%). Baseline resistance-conferring variants in NS3 were rare. M28V in GT1a and Y93H in GT1b were the most prevalent preexisting variants in NS5A, and C316N in GT1b and S556G in both GT1a and GT1b were the most prevalent variants in NS5B. Interestingly, all the GT1a sequences encoding M28V in NS5A were from the United States, while GT1b sequences encoding C316N and S556G in NS5B were predominant in the European Union. Variants preexisting at baseline had no significant impact on treatment outcome. The most prevalent treatment-emergent resistance-associated variants (RAVs) in GT1a were R155K and D168V in NS3, M28T and Q30R in NS5A, and S556G in NS5B. The single GT1b-infected patient experiencing virologic failure had no RAVs in any target. A paritaprevir-ritonavir dose of 150/100 mg was more efficacious in suppressing R155K in NS3 than a 100/100-mg dose. In patients who failed after receiving 12 or more weeks of treatment, RAVs were selected in all 3 targets, while most patients who relapsed after 8 weeks of treatment did so without any detectable RAVs. Results from this study guided the selection of the optimal treatment regimen, treatment duration, and paritaprevir dose for further development of the 3D regimen. (This study has been registered at ClinicalTrials.gov under registration number NCT01464827.).

摘要

“飞行员”(AVIATOR)是一项2期临床试验,在406例丙型肝炎病毒1型(GT1)感染患者中,评估了利托那韦增强的帕立普韦(一种蛋白酶抑制剂)、奥比他韦(一种NS5A抑制剂)和达沙布韦(一种非核苷聚合酶抑制剂)(三联疗法)联合或不联合利巴韦林(RBV)治疗8周、12周或24周的疗效。在三联疗法联合或不联合RBV的各个治疗组中,治疗24周后的持续病毒学应答率在88%至100%之间;20例GT1a感染患者和1例GT1b感染患者出现病毒学失败(5.2%)。NS3中基线时赋予耐药性的变异罕见。GT1a中的M28V和GT1b中的Y93H是NS5A中最常见的预先存在的变异,GT1b中的C316N以及GT1a和GT1b中的S556G是NS5B中最常见的变异。有趣的是,所有编码NS5A中M28V的GT1a序列均来自美国,而编码NS5B中C316N和S556G的GT1b序列在欧盟最为常见。基线时预先存在的变异对治疗结果无显著影响。GT1a中最常见的治疗中出现的耐药相关变异(RAV)是NS3中的R155K和D168V、NS5A中的M28T和Q30R以及NS5B中的S556G。那例出现病毒学失败的GT1b感染患者在任何靶点均未出现RAV。150/100 mg的帕立普韦 - 利托那韦剂量在抑制NS3中的R155K方面比100/100 mg剂量更有效。在接受12周或更长时间治疗后失败的患者中,所有3个靶点均出现了RAV,而大多数在8周治疗后复发的患者复发时未检测到任何RAV。本研究结果为三联疗法的进一步研发指导了最佳治疗方案、治疗疗程和帕立普韦剂量的选择。(本研究已在ClinicalTrials.gov注册,注册号为NCT01464827。)

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f73/4538512/b710b033cea0/zac0091543120001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f73/4538512/b710b033cea0/zac0091543120001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f73/4538512/b710b033cea0/zac0091543120001.jpg

相似文献

1
Resistance analysis of baseline and treatment-emergent variants in hepatitis C virus genotype 1 in the AVIATOR study with paritaprevir-ritonavir, ombitasvir, and dasabuvir.在使用帕利哌韦-利托那韦、奥比他韦和达沙布韦的AVIATOR研究中,丙型肝炎病毒1型基线和治疗中出现的变异的耐药性分析。
Antimicrob Agents Chemother. 2015 Sep;59(9):5445-54. doi: 10.1128/AAC.00998-15. Epub 2015 Jun 22.
2
Analysis of Hepatitis C Virus Genotype 1b Resistance Variants in Japanese Patients Treated with Paritaprevir-Ritonavir and Ombitasvir.接受帕利瑞韦-利托那韦和奥比他韦治疗的日本患者丙型肝炎病毒1b基因型耐药变异分析
Antimicrob Agents Chemother. 2015 Dec 7;60(2):1106-13. doi: 10.1128/AAC.02606-15. Print 2016 Feb.
3
Ombitasvir/paritaprevir/ritonavir and dasabuvir tablets for hepatitis C virus genotype 1 infection.用于丙型肝炎病毒1型感染的奥比他韦/帕利哌韦/利托那韦和达沙布韦片
Ann Pharmacother. 2015 May;49(5):566-81. doi: 10.1177/1060028015570729. Epub 2015 Feb 13.
4
Shortened therapy of eight weeks with paritaprevir/ritonavir/ombitasvir and dasabuvir is highly effective in people with recent HCV genotype 1 infection.对于近期感染丙型肝炎病毒1型的患者,使用帕利瑞韦/利托那韦/奥米他韦和达沙布韦进行为期八周的缩短疗程治疗具有很高的疗效。
J Viral Hepat. 2018 Oct;25(10):1180-1188. doi: 10.1111/jvh.12917. Epub 2018 May 8.
5
Resistance characterization of hepatitis C virus genotype 2 from Japanese patients treated with ombitasvir and paritaprevir/ritonavir.日本患者采用奥比他韦和帕利瑞韦/利托那韦治疗后的 HCV 基因 2 型耐药特征。
J Med Virol. 2018 Jan;90(1):109-119. doi: 10.1002/jmv.24923. Epub 2017 Sep 22.
6
Ombitasvir/paritaprevir/ritonavir+dasabuvir+ribavirin for chronic hepatitis C virus genotype 1b-infected cirrhotics (TURQUOISE-IV).奥比他韦/帕利瑞韦/利托那韦+达沙布韦+利巴韦林用于治疗慢性丙型肝炎病毒1b型感染的肝硬化患者(TURQUOISE-IV研究)
Eur J Gastroenterol Hepatol. 2018 Sep;30(9):1073-1076. doi: 10.1097/MEG.0000000000001166.
7
ABT-450, ritonavir, ombitasvir, and dasabuvir achieves 97% and 100% sustained virologic response with or without ribavirin in treatment-experienced patients with HCV genotype 1b infection.ABT-450、利托那韦、奥比他韦和达沙布韦联合或不联合利巴韦林在治疗慢性丙型肝炎 1b 型感染的有治疗经验的患者中实现了 97%和 100%的持续病毒学应答。
Gastroenterology. 2014 Aug;147(2):359-365.e1. doi: 10.1053/j.gastro.2014.04.045. Epub 2014 May 9.
8
Drug-Drug Interactions between Sofosbuvir and Ombitasvir-Paritaprevir-Ritonavir with or without Dasabuvir.索磷布韦与奥比他韦-帕利瑞韦-利托那韦联用(无论是否联用达沙布韦)时的药物相互作用。
Antimicrob Agents Chemother. 2015 Nov 23;60(2):855-61. doi: 10.1128/AAC.01913-15. Print 2016 Feb.
9
Ombitasvir, paritaprevir co-dosed with ritonavir, dasabuvir, and ribavirin for hepatitis C in patients co-infected with HIV-1: a randomized trial.奥比他韦、帕利瑞韦与利托那韦联合达沙布韦和利巴韦林治疗 HIV-1 合并丙型肝炎病毒感染患者的随机试验。
JAMA. 2015;313(12):1223-31. doi: 10.1001/jama.2015.1328.
10
Exposure-Efficacy Analyses of Ombitasvir, Paritaprevir/Ritonavir with Dasabuvir ± Ribavirin in HCV Genotype 1-Infected Patients.奥比他韦、帕利哌韦/利托那韦联合达沙布韦±利巴韦林治疗丙型肝炎病毒1型感染患者的暴露-疗效分析
Clin Drug Investig. 2016 Aug;36(8):625-35. doi: 10.1007/s40261-016-0407-x.

引用本文的文献

1
Viral proteases as therapeutic targets.病毒蛋白酶作为治疗靶点。
Mol Aspects Med. 2022 Dec;88:101159. doi: 10.1016/j.mam.2022.101159. Epub 2022 Nov 29.
2
Molecular Epidemiology and Baseline Resistance of Hepatitis C Virus to Direct Acting Antivirals in Croatia.克罗地亚丙型肝炎病毒的分子流行病学及对直接作用抗病毒药物的基线耐药性
Pathogens. 2022 Jul 19;11(7):808. doi: 10.3390/pathogens11070808.
3
The Role of RASs /RVs in the Current Management of HCV.RASs /RVs 在 HCV 现行管理中的作用。

本文引用的文献

1
In vitro activity and resistance profile of dasabuvir, a nonnucleoside hepatitis C virus polymerase inhibitor.非核苷类丙型肝炎病毒聚合酶抑制剂达沙布韦的体外活性及耐药谱
Antimicrob Agents Chemother. 2015 Mar;59(3):1505-11. doi: 10.1128/AAC.04619-14. Epub 2014 Dec 22.
2
In vitro and in vivo antiviral activity and resistance profile of ombitasvir, an inhibitor of hepatitis C virus NS5A.丙肝病毒NS5A抑制剂ombitasvir的体外和体内抗病毒活性及耐药性分析
Antimicrob Agents Chemother. 2015 Feb;59(2):979-87. doi: 10.1128/AAC.04226-14. Epub 2014 Dec 1.
3
In vitro and in vivo antiviral activity and resistance profile of the hepatitis C virus NS3/4A protease inhibitor ABT-450.
Viruses. 2021 Oct 18;13(10):2096. doi: 10.3390/v13102096.
4
HCV Replicon Systems: Workhorses of Drug Discovery and Resistance.丙型肝炎病毒复制子系统:药物研发与耐药性研究的主力军
Front Cell Infect Microbiol. 2020 Jun 30;10:325. doi: 10.3389/fcimb.2020.00325. eCollection 2020.
5
Factors Influencing the Prevalence of Resistance-Associated Substitutions in NS5A Protein in Treatment-Naive Patients with Chronic Hepatitis C.影响初治慢性丙型肝炎患者NS5A蛋白耐药相关替代发生率的因素
Biomedicines. 2020 Apr 7;8(4):80. doi: 10.3390/biomedicines8040080.
6
Lower Rates Of Naturally Occurring Resistance-Associated Substitutions (RASs) In Hepatitis C Virus (HCV)-Infected Chronic Kidney Disease (CKD) Patients Than In HCV-Infected Patients With Only Liver Disease.丙型肝炎病毒(HCV)感染的慢性肾脏病(CKD)患者中自然发生的耐药相关替代(RASs)率低于仅患有肝病的HCV感染患者。
Infect Drug Resist. 2019 Nov 22;12:3635-3640. doi: 10.2147/IDR.S220335. eCollection 2019.
7
Exploring the hepatitis C virus genome using single molecule real-time sequencing.利用单分子实时测序技术探索丙型肝炎病毒基因组。
World J Gastroenterol. 2019 Aug 28;25(32):4661-4672. doi: 10.3748/wjg.v25.i32.4661.
8
Opciones terapéuticas para los pacientes con hepatitis C crónica y fracaso terapéutico previo.丙型肝炎慢性患者及既往治疗失败患者的治疗选择
Clin Liver Dis (Hoboken). 2016 Nov 10;8(Suppl 1):S25-S29. doi: 10.1002/cld.594. eCollection 2016 Nov.
9
Treatment options of patients with chronic hepatitis C who have failed prior therapy.既往治疗失败的慢性丙型肝炎患者的治疗选择。
Clin Liver Dis (Hoboken). 2016 Feb 26;7(2):40-44. doi: 10.1002/cld.532. eCollection 2016 Feb.
10
Resistance testing: Interpretation and incorporation into HCV treatment algorithms.耐药性检测:解读及其纳入丙型肝炎治疗方案
Clin Liver Dis (Hoboken). 2017 May 26;9(5):115-120. doi: 10.1002/cld.631. eCollection 2017 May.
丙型肝炎病毒NS3/4A蛋白酶抑制剂ABT-450的体外和体内抗病毒活性及耐药性概况
Antimicrob Agents Chemother. 2015 Feb;59(2):988-97. doi: 10.1128/AAC.04227-14. Epub 2014 Dec 1.
4
Global origin and transmission of hepatitis C virus nonstructural protein 3 Q80K polymorphism.丙型肝炎病毒非结构蛋白3 Q80K多态性的全球起源与传播
J Infect Dis. 2015 Apr 15;211(8):1288-95. doi: 10.1093/infdis/jiu613. Epub 2014 Nov 10.
5
Simeprevir with pegylated interferon alfa 2a or 2b plus ribavirin in treatment-naive patients with chronic hepatitis C virus genotype 1 infection (QUEST-2): a randomised, double-blind, placebo-controlled phase 3 trial.西美瑞韦联合聚乙二醇干扰素 α-2a 或 -2b 加利巴韦林治疗初治慢性丙型肝炎病毒基因 1 型感染患者(QUEST-2):一项随机、双盲、安慰剂对照的 3 期临床试验。
Lancet. 2014 Aug 2;384(9941):414-26. doi: 10.1016/S0140-6736(14)60538-9. Epub 2014 Jun 4.
6
ABT-450, ritonavir, ombitasvir, and dasabuvir achieves 97% and 100% sustained virologic response with or without ribavirin in treatment-experienced patients with HCV genotype 1b infection.ABT-450、利托那韦、奥比他韦和达沙布韦联合或不联合利巴韦林在治疗慢性丙型肝炎 1b 型感染的有治疗经验的患者中实现了 97%和 100%的持续病毒学应答。
Gastroenterology. 2014 Aug;147(2):359-365.e1. doi: 10.1053/j.gastro.2014.04.045. Epub 2014 May 9.
7
ABT-450/r-ombitasvir and dasabuvir with or without ribavirin for HCV.ABT-450/r-ombitasvir 和 dasabuvir 联合或不联合利巴韦林治疗 HCV。
N Engl J Med. 2014 May 22;370(21):1983-92. doi: 10.1056/NEJMoa1402338. Epub 2014 May 4.
8
ABT-450/r-ombitasvir and dasabuvir with ribavirin for hepatitis C with cirrhosis.ABT-450/r-ombitasvir 和 dasabuvir 联合利巴韦林治疗肝硬化合并丙型肝炎。
N Engl J Med. 2014 May 22;370(21):1973-82. doi: 10.1056/NEJMoa1402869. Epub 2014 Apr 11.
9
Treatment of HCV with ABT-450/r-ombitasvir and dasabuvir with ribavirin.ABT-450/r-ombitasvir 和利巴韦林联合治疗 HCV。
N Engl J Med. 2014 Apr 24;370(17):1594-603. doi: 10.1056/NEJMoa1315722. Epub 2014 Apr 10.
10
Retreatment of HCV with ABT-450/r-ombitasvir and dasabuvir with ribavirin.ABT-450/r-ombitasvir 和 dasabuvir 联合利巴韦林治疗 HCV。
N Engl J Med. 2014 Apr 24;370(17):1604-14. doi: 10.1056/NEJMoa1401561. Epub 2014 Apr 10.