期刊文献+

恩替卡韦经治HBeAg阴性慢性乙肝患者联合聚乙二醇干扰素α-2b治疗的临床治愈疗效观察 被引量:7

The clinical cure efficacy of peginterferonα-2b add-on therapy in entecavir-treated patients with HBeAg-negative chronic hepatitis B
下载PDF
导出
摘要 目的观察恩替卡韦经治HBeAg阴性慢性乙肝患者联合PEG-IFNα-2b治疗后HBsAg清除率。方法选取2017年4月至2018年6月就诊于厦门长庚医院的146例乙肝患者,根据不同治疗方式分为联合治疗组(恩替卡韦+PEG-IFNα-2b治疗,n=44)和恩替卡韦单药组(恩替卡韦治疗,n=102),比较两组HBsAg清除率和血清学转换率。结果联合治疗组有4例在24周时终止Peg-IFNα-2b治疗,24周时8例HBsAg阴转,3例发生HBsAg血清转换;48周时12例HBsAg阴转,6例HBsAg发生血清转换;23例HBsAg下降<1log,停PEG-IFNα-2b继续恩替卡韦治疗;其中5例HBsAg下降≥1log继续PEG-IFNα-2b及恩替卡韦治疗至72周,72周时累计15例HBsAg阴转(女4例,男11例),累计9例HBsAg发生血清转换,临床治愈率34.1%。其中,HBsAg滴度基线<350 IU/ml,12例获得临床治愈;联合治疗24周时HBsAg较基线下降≥1log,15例获得临床治愈。恩替卡韦单药组治疗72周,1例HBsAg阴转,临床治愈率为0.9%。无HBsAg血清转换发生。结论恩替卡韦经治HBeAg阴性慢性乙肝患者,联合PEG-IFNα-2b可显著提高HBsAg阴转率,获得临床治愈,其中HBsAg滴度基线<350 IU/ML、联合治疗24周HBsAg较基线下降≥1log的患者更易获得临床治愈。 Objective To observe the HBsAg loss rate of PEG-IFNα-2 b add-on therapy in entecavir(ETV)-treated patients with HBeAg-negative chronic hepatitis B.Methods 146 patients with hepatitis B who met the inclusion criteria and met the inclusion criteria in Xiamen Changgeng Hospital from April 2017 to June 2018 were selected,and they were divided into the combined treatment group(entecavir+PEG-IFNα-2 b treatment,n=44)and the entecavir monotherapy group(entecavir treatment,n=102),and the clearance rate and serological conversion rate between the two group were compared.Results 44 patients in the combined treatment group stopped PEG-IFNα-2 B treatment at 24 weeks,8 patients had HBsAg negative conversion,and 3 patients had HBsAg seroconversion at 24 weeks.At 48 weeks,12 patients had HBsAg negative conversion,and 6 patients had HBsAg seroconversion.23 patients with HBsAg decrease<1 log stopped PEG-IFNα-2 b and continued entecavir treatment;Five patients with HBsAg decrease≥1 log were continued with PEG-IFNα-2 b and entecavir treatment until 72 weeks.At the end of 72 weeks,15 patients(4 females,11 males)had HBsAg negative conversion,and 9 patients had seroconversion.The clinical cure rate was 34.1%.Among them,HBsAg titer baseline<350 IU/mL,12 cases were clinically cured;at 24 weeks of combined therapy,HBsAg decreased≥1 log from baseline,and 15 patients were clinically cured.In the entecavir monotherapy group,all patients were treated for 72 weeks,and 1 patient had negative HBsAg transformation.The clinical cure rate was 0.9%.No HBsAg seroconversion occurred.Conclusion PEG-IFNα-2 b significantly increased HBsAg loss rates of entecavir-treated patients with HBeAg-negative chronic hepatitis B,and the clinical cure can be achieved easier in patients with baseline HBsAg<350 IU/mL and/or a decrease of HBsAg≥1 log from baseline to 24 weeks of combination therapy.
作者 赵海东 陈婷婷 李艺芳 苏惠珍 林巧欣 ZHAO Haidong;CHEN Tingting;LI Yifang;SU Huizhen;LIN Qiaoxin(Department of Infection,Xiamen Changgeng Hospital,Fujian Province,Xiamen,Fujian,361026,China)
出处 《当代医学》 2021年第21期96-98,共3页 Contemporary Medicine
关键词 HBEAG阴性慢性乙型肝炎 聚乙二醇干扰素Α-2B 恩替卡韦 临床治愈 HBeAg negativehepatitis B PEG-IFNα-2b Entecavir Clinical cure
  • 相关文献

参考文献5

二级参考文献51

  • 1Lai CL,Shouval D,Lok AS,陈楠(摘译),张占卿(审校).恩替卡韦与拉米夫定治疗HBeAg阴性慢性乙型肝炎的对照研究[J].世界感染杂志,2006,6(4):396-396. 被引量:201
  • 2Liang X, Bi S, Yang W, et al. Evaluation of the impact of hepatitis B vaccination among children born during 1992-2005 in China. J Infect Dis[J], 2009, 200(1) : 39-47.
  • 3Yan H, Zhong G, Xu G, et al. Sodium taurocholate co- transporting polypeptide is a functional receptor for hu- man hepatitis B and D virus [ J ]. elife, 2012, 1 : e00049.
  • 4Watashi K, Sluder A, Daito T, et al. Cyclosporin A and its analogs inhibit hepatitis B virus entry into cultured hepatocytes through targeting a membrane transporter NT-CP[J]. Hepatology, 2014, 59(5):1726-1737.
  • 5Nkongolo, S, Ni Y, Lempp FA, et al. Cyclosporin A inhibits Hepatitis B and Hepatitis D Virus entry by Cy- elophilin-independent interference with the NTCP recep- tor[J]. J Hepatol, 2014, 60(4):723-31.
  • 6Lucifora J, Esser K, Protzer U. Ezetimibe blocks hepa- titis B virus infection after virus uptake into hepatocytes [J]. Antiviral Res, 2013, 97(2), 195-197.
  • 7Ni Y, Lempp FA, Mebrle S, et al. Hepatitis B and D viruses exploit sodium taurocholate co-transporting poly- peptide for species-specific entry into hepatocytes [ J ]. Gastroenterology,2014, 146( 1 ) :1070-1083.
  • 8Watashi K, Sluder A, Daito T, et al. Cyclosporin A and its analogs inhibit hepatitis B virus entry into cul- tured hepatocytes through targeting a membrane trans- porter NTCP [ J ]. Hepatology, 2014, 59 ( 5 ) : 1726 -1737.
  • 9Yan H, Peng B, Lin Y, et al. Viral entry of Hepatitis B and D viruses and bile salts transportation share common molecular determinants on sodium taurocbolate cotrans- porting polypeptide [ J ]. J Virol, 2014, 88 ( 6 ) : 3273-3284.
  • 10Liaw YF, Jia JD, Chan HL, et al. Shorter durations and lower doses of peginterferon alfa-2a are associated with inferior hepatitis B e antigen seroconversion rates in hepatitis B virus genotypes B or C. Hepatology 2011; 54 : 1591-1599.

共引文献1122

同被引文献84

引证文献7

二级引证文献5

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部