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EASL Clinical Practice Guidelines: management of hepatitis C virus infection.欧洲肝脏研究学会临床实践指南:丙型肝炎病毒感染的管理
J Hepatol. 2014 Feb;60(2):392-420. doi: 10.1016/j.jhep.2013.11.003. Epub 2013 Dec 9.
2
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Rev Recent Clin Trials. 2014;9(1):1-7. doi: 10.2174/1574887108666131213120354.
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Concomitant interferon-alpha and chemotherapy in hepatitis C and colorectal cancer: a case report.干扰素-α与化疗联合应用于丙型肝炎合并结直肠癌:1 例报告。
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[Epidemiology of hepatitis A, B, and C among adults in Germany: results of the German Health Interview and Examination Survey for Adults (DEGS1)].德国成年人甲型、乙型和丙型肝炎的流行病学:德国成年人健康访谈与检查调查(DEGS1)结果
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Sofosbuvir for previously untreated chronic hepatitis C infection.索磷布韦片治疗未经治疗的慢性丙型肝炎感染。
N Engl J Med. 2013 May 16;368(20):1878-87. doi: 10.1056/NEJMoa1214853. Epub 2013 Apr 23.
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Sofosbuvir for hepatitis C genotype 2 or 3 in patients without treatment options.索磷布韦用于无治疗选择的 2 或 3 型丙型肝炎病毒感染患者。
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Nucleotide polymerase inhibitor sofosbuvir plus ribavirin for hepatitis C.核苷酸聚合酶抑制剂索非布韦联合利巴韦林治疗丙型肝炎。
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慢性丙型肝炎感染患者对聚乙二醇干扰素α-2a/利巴韦林反应的年龄相关差异。

Age-related differences in response to peginterferon alfa-2a/ribavirin in patients with chronic hepatitis C infection.

作者信息

Roeder Claudia, Jordan Sabine, Schulze Zur Wiesch Julian, Pfeiffer-Vornkahl Heike, Hueppe Dietrich, Mauss Stefan, Zehnter Elmar, Stoll Sabine, Alshuth Ulrich, Lohse Ansgar W, Lueth Stefan

机构信息

Claudia Roeder, Sabine Jordan, Julian Schulze zur Wiesch, Ansgar W Lohse, Stefan Lueth, Department of Medicine I, University Hospital Hamburg Eppendorf, 20246 Hamburg, Germany.

出版信息

World J Gastroenterol. 2014 Aug 21;20(31):10984-93. doi: 10.3748/wjg.v20.i31.10984.

DOI:10.3748/wjg.v20.i31.10984
PMID:25152602
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4138479/
Abstract

AIM

To evaluate the safety and efficacy of pegylated interferon alfa-2a and ribavirin therapy in elderly patients with chronic hepatitis C infection.

METHODS

Patients characteristics, treatment results and safety profiles of 4859 patients with hepatitis c virus (HCV) infection receiving treatment with pegylated interferon alfa-2a and ribavirin were retrieved from a large ongoing German multicentre non-interventional study. Recommended treatment duration was 24 wk for GT 2 and GT 3 infection and 48 wk for GT 1 and GT 4 infection. Patients were stratified according to age (< 60 years vs ≥ 60 years). Because of limited numbers of liver biopsies for further assessment of liver fibrosis APRI (aspartate aminotransferase - platelet ratio index) was performed using pre-treatment laboratory data.

RESULTS

Out of 4859 treated HCV patients 301 (6.2%) were ≥ 60 years. There were more women (55.8% vs 34.2%, P < 0.001) and predominantly GT 1 (81.4% vs 57.3%, P < 0.001) infected patients in the group of patients aged ≥ 60 years and they presented more frequently with metabolic (17.6% vs 4.5%, P < 0.001) and cardiovascular comorbidities (32.6% vs 6.7%, P < 0.001) and significant fibrosis and cirrhosis (F3/4 31.1% vs 14.0%, P = 0.0003). Frequency of dose reduction and treatment discontinuation were significantly higher in elderly patients (30.9% vs 13.7%, P < 0.001 and 47.8% vs 30.8%, P < 0.001). Main reason for treatment discontinuation was "virological non-response" (26.6% vs 13.6%). Sustained virological response (SVR) rates showed an age related difference in patients with genotype 1 (23.7% vs 43.7%, P < 0.001) but not in genotype 2/3 infections (57.7% vs 64.6%, P = 0.341). By multivariate analysis, age and stage of liver disease were independent factors of SVR.

CONCLUSION

Elderly HCV patients differ in clinical characteristics and treatment outcome from younger patients and demand special attention from their practitioner.

摘要

目的

评估聚乙二醇化干扰素α-2a联合利巴韦林治疗老年慢性丙型肝炎感染患者的安全性和疗效。

方法

从一项正在进行的大型德国多中心非干预性研究中检索4859例接受聚乙二醇化干扰素α-2a联合利巴韦林治疗的丙型肝炎病毒(HCV)感染患者的特征、治疗结果和安全性资料。推荐的治疗疗程为基因2型和基因3型感染24周,基因1型和基因4型感染48周。患者按年龄分层(<60岁与≥60岁)。由于用于进一步评估肝纤维化的肝活检数量有限,因此使用治疗前实验室数据计算天冬氨酸氨基转移酶-血小板比率指数(APRI)。

结果

在4859例接受治疗的HCV患者中,301例(6.2%)年龄≥60岁。≥60岁患者组中女性更多(55.8%对34.2%,P<0.001),主要为基因1型感染(81.4%对57.3%,P<0.001),且代谢合并症(17.6%对4.5%,P<0.001)、心血管合并症(32.6%对6.7%,P<0.001)以及显著纤维化和肝硬化(F3/4 31.1%对14.0%,P=0.0003)更为常见。老年患者剂量减少和治疗中断的频率显著更高(30.9%对13.7%,P<0.001和47.8%对30.8%,P<0.001)。治疗中断的主要原因是“病毒学无应答”(26.6%对13.6%)。基因1型患者的持续病毒学应答(SVR)率存在年龄相关差异(23.7%对43.7%,P<0.001),但基因2/3型感染患者中无此差异(57.7%对64.6%,P=0.341)。多因素分析显示,年龄和肝病分期是SVR的独立影响因素。

结论

老年HCV患者在临床特征和治疗结果方面与年轻患者不同,需要从业者给予特别关注。