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1
Management of untreated and nonresponder patients with chronic hepatitis C.慢性丙型肝炎未治疗和无应答患者的管理。
Semin Liver Dis. 2010 Nov;30(4):348-60. doi: 10.1055/s-0030-1267536. Epub 2010 Oct 19.
2
Peginterferon alfa-2a (40KD) (PEGASYS) plus ribavirin (COPEGUS) in retreatment of chronic hepatitis C patients, nonresponders and relapsers to previous conventional interferon plus ribavirin therapy.聚乙二醇干扰素α-2a(40KD)(派罗欣)联合利巴韦林(Copegus)用于既往接受过传统干扰素联合利巴韦林治疗无应答和复发的慢性丙型肝炎患者的再治疗。
Braz J Infect Dis. 2006 Feb;10(1):11-6. doi: 10.1590/s1413-86702006000100003. Epub 2006 Jun 2.
3
Treatment of dialysis patients with chronic hepatitis C using pegylated interferon and low-dose ribavirin.使用聚乙二醇化干扰素和小剂量利巴韦林治疗慢性丙型肝炎的透析患者。
Int J Artif Organs. 2008 Apr;31(4):295-302. doi: 10.1177/039139880803100404.
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The clinical effectiveness of pegylated interferon and ribavirin for the treatment of chronic hepatitis C in HIV-infected patients in Brazil: a multicentric study.聚乙二醇干扰素和利巴韦林治疗巴西HIV感染患者慢性丙型肝炎的临床疗效:一项多中心研究。
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5
Antiviral regimen complexity index as an independent predictor of sustained virologic response in patients with chronic hepatitis C.抗病毒治疗方案复杂性指数作为慢性丙型肝炎患者持续病毒学应答的独立预测指标
J Manag Care Pharm. 2013 Jul-Aug;19(6):448-53. doi: 10.18553/jmcp.2013.19.6.448.
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Sustained virological response: a milestone in the treatment of chronic hepatitis C.持续病毒学应答:慢性丙型肝炎治疗的里程碑。
World J Gastroenterol. 2013 May 14;19(18):2793-8. doi: 10.3748/wjg.v19.i18.2793.
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High-dose pegylated interferon-α and ribavirin in nonresponder hepatitis C patients and relationship with IL-28B genotype (SYREN trial).大剂量聚乙二醇干扰素-α和利巴韦林治疗无应答丙型肝炎患者与 IL-28B 基因型的关系(SYREN 试验)。
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8
Retreatment of hepatitis C patients with pegylated interferon combined with ribavirin in non-responders to interferon plus ribavirin. Is it different in real life?聚乙二醇干扰素联合利巴韦林治疗干扰素联合利巴韦林无应答的丙型肝炎患者。在现实生活中是否有所不同?
BMC Infect Dis. 2010 Jul 20;10:212. doi: 10.1186/1471-2334-10-212.
9
Re-treatment of patients with hepatitis C who failed to respond (nonresponders) to previous treatment.对先前治疗无反应(无反应者)的丙型肝炎患者进行再治疗。
Georgian Med News. 2009 Jan(166):61-4.
10
[Diagnosis and treatment of chronic hepatitis C. Practical recommendations and new developments].[慢性丙型肝炎的诊断与治疗。实用建议与新进展]
Med Klin (Munich). 2001 Oct 15;96(10):599-607. doi: 10.1007/s00063-001-1094-8.

本文引用的文献

1
Chronic hepatitis C of 28 years' duration characterized by early development of stage 2 (of 4) fibrosis but no significant progression over the subsequent 18 years.病程28年的慢性丙型肝炎,其特征为早期(共4期)出现2期纤维化,但在随后18年中无显著进展。
Semin Liver Dis. 2010 Aug;30(3):302-9. doi: 10.1055/s-0030-1262516. Epub 2010 Jul 21.
2
Outcome of sustained virological responders with histologically advanced chronic hepatitis C.组织学上慢性丙型肝炎进展期持续病毒学应答者的结局。
Hepatology. 2010 Sep;52(3):833-44. doi: 10.1002/hep.23744.
3
Multiple effects of silymarin on the hepatitis C virus lifecycle.水飞蓟素对丙型肝炎病毒生命周期的多种影响。
Hepatology. 2010 Jun;51(6):1912-21. doi: 10.1002/hep.23587.
4
Isolation and identification of ester impurities in RG7128, an HCV polymerase inhibitor.RG7128 中酯杂质的分离与鉴定,一种 HCV 聚合酶抑制剂。
J Pharm Biomed Anal. 2010 Nov 2;53(3):710-6. doi: 10.1016/j.jpba.2010.04.003. Epub 2010 Apr 9.
5
Telaprevir for previously treated chronic HCV infection.替拉瑞韦治疗既往治疗的慢性 HCV 感染。
N Engl J Med. 2010 Apr 8;362(14):1292-303. doi: 10.1056/NEJMoa0908014.
6
Sustained virologic response prevents the development of esophageal varices in compensated, Child-Pugh class A hepatitis C virus-induced cirrhosis. A 12-year prospective follow-up study.持续病毒学应答可预防代偿期、Child-Pugh 分级为 A 的丙型肝炎病毒相关性肝硬化食管静脉曲张的发展。一项 12 年的前瞻性随访研究。
Hepatology. 2010 Jun;51(6):2069-76. doi: 10.1002/hep.23528.
7
Replicated association between an IL28B gene variant and a sustained response to pegylated interferon and ribavirin.IL28B 基因变异与聚乙二醇干扰素和利巴韦林持续应答的复制关联。
Gastroenterology. 2010 Jun;138(7):2307-14. doi: 10.1053/j.gastro.2010.02.009. Epub 2010 Feb 19.
8
Review article: optimizing SVR and management of the haematological side effects of peginterferon/ribavirin antiviral therapy for HCV - the role of epoetin, G-CSF and novel agents.综述文章:聚乙二醇干扰素/利巴韦林抗病毒治疗 HCV 引起的血液学不良反应的优化治疗和管理——促红细胞生成素、G-CSF 及新型药物的作用。
Aliment Pharmacol Ther. 2010 May;31(9):929-37. doi: 10.1111/j.1365-2036.2010.04269.x. Epub 2010 Feb 18.
9
Genetic variation in IL28B is associated with chronic hepatitis C and treatment failure: a genome-wide association study.IL28B 基因变异与慢性丙型肝炎及治疗失败相关:一项全基因组关联研究。
Gastroenterology. 2010 Apr;138(4):1338-45, 1345.e1-7. doi: 10.1053/j.gastro.2009.12.056. Epub 2010 Jan 11.
10
IL28B is associated with response to chronic hepatitis C interferon-alpha and ribavirin therapy.IL28B与慢性丙型肝炎α干扰素和利巴韦林治疗的反应相关。
Nat Genet. 2009 Oct;41(10):1100-4. doi: 10.1038/ng.447. Epub 2009 Sep 13.

慢性丙型肝炎未治疗和无应答患者的管理。

Management of untreated and nonresponder patients with chronic hepatitis C.

机构信息

National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD, USA.

出版信息

Semin Liver Dis. 2010 Nov;30(4):348-60. doi: 10.1055/s-0030-1267536. Epub 2010 Oct 19.

DOI:10.1055/s-0030-1267536
PMID:20960375
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7464570/
Abstract

Hepatitis C infection has evolved in the past quarter century from a newly recognized entity without a known pathogen (non-A, non-B hepatitis) to one of the world's most prevalent causes of liver disease, an important source for hepatocellular carcinoma, and the major indication for liver transplantation. It is caused by a virus with a complex replication cycle that occurs in multiple genotypes, of which the four most prevalent (1, 2, 3, and 4) exhibit differences in clinical behavior and responses to therapy. Chronic hepatitis C virus (HCV) in particular has evolved from a disease with no known treatment to one with several primary treatment options, none of which is uniformly effective, and a growing list of secondary treatment options for those who have failed to respond to, or relapsed after initial therapy. As treatment is often associated with significant side effects, it is now a disease that presents clinicians with multiple important decisions: whom to treat, when and with what to treat them initially, and how to manage patients who have failed during initial therapy to achieve a sustained virological response, the gold standard of effective therapy. This review examines each of these important decisions, presenting evidence to help guide clinicians in their choices. The decisions are addressed sequentially as they arise during the initial evaluation and subsequent treatment of a typical, newly recognized patient with chronic HCV, and the considerations facing the clinician when the patient has failed to achieve an SVR.

摘要

丙型肝炎感染在过去的四分之一个世纪中已经从一种新发现的、没有已知病原体的疾病(非甲、非乙型肝炎)发展成为世界上最常见的肝脏疾病病因之一,也是肝细胞癌的重要来源,以及肝移植的主要指征。它是由一种具有复杂复制周期的病毒引起的,该病毒存在多种基因型,其中最常见的四种(1、2、3 和 4)在临床行为和对治疗的反应方面存在差异。特别是慢性丙型肝炎病毒(HCV)已经从一种没有已知治疗方法的疾病发展为有几种主要治疗选择的疾病,这些治疗方法都不是完全有效的,并且对于那些对初始治疗没有反应或初始治疗后复发的患者,治疗方法的选择也越来越多。由于治疗通常伴随着明显的副作用,因此现在丙型肝炎已经成为一种需要临床医生做出多个重要决策的疾病:治疗哪些患者,何时开始治疗以及用什么方法治疗,以及如何管理那些在初始治疗中未能实现持续病毒学应答(有效治疗的金标准)的患者。这篇综述探讨了这些重要决策中的每一个,提供了证据来帮助指导临床医生做出选择。这些决策是在对一名新确诊的慢性丙型肝炎患者进行初始评估和后续治疗时逐步提出的,并且还考虑了在患者未能实现 SVR 时临床医生所面临的问题。