...
首页> 外文期刊>Journal of Infection >The effects of a maintenance therapy with peg-interferon alpha-2a on liver fibrosis in HIV/HCV co-infected patients: A randomized controlled trial
【24h】

The effects of a maintenance therapy with peg-interferon alpha-2a on liver fibrosis in HIV/HCV co-infected patients: A randomized controlled trial

机译:聚乙二醇干扰素α-2a维持疗法对HIV / HCV合并感染患者肝纤维化的影响:一项随机对照试验

获取原文
获取原文并翻译 | 示例
           

摘要

Objective: We hypothesized that, in Human Immunodeficiency Virus and Hepatitis C Virus (HIV/HCV) co-infected patients who did not respond to peg-interferon and ribavirin, a maintenance therapy with peg-interferon could induce fibrosis regression. Methods: This was a randomized study with two parallel groups. HIV/HCV co-infected patients received peg-interferon α-2a at 180μg/week or remained on observation for 96 weeks. The primary endpoint was the percentage of patients who experienced a decrease of at least one point in their Metavir fibrosis score between initial and final liver biopsies. Secondary endpoints included plasma fibrosis markers at week 96, occurrence of HCV-related complications, and survival. Results: A total of 52 patients were randomized (peg-interferon: 25; control: 27) including 18 with cirrhosis. The median (interquartile range) age was 44 (40-46) years, and 69% were male. A total of 64% had ALT levels 1.5 normal values, and the CD4 cell count was 391 (296-537)cells/mm3; 67% of patients had HIV RNA 200copies/mL at entry. The main endpoint was assessed in 41 patients. Response rates were 3/20 (15%) and 4/21 (19%) in the peg-interferon and control groups, respectively (p=0.99). There was no significant difference between peg-interferon and control groups on plasma fibrosis markers at the final visit. Severe liver-related complications were observed in 2 and 5 patients in peg-interferon and control groups, respectively. Three deaths were observed, all in the control group. Conclusions: A maintenance therapy with peg-interferon α-2a over 96 weeks in HIV/HCV co-infected patients, who were non-responders to HCV treatment, did not change liver fibrosis. ClinicalTrials.gov Identifier: NCT00122616.
机译:目的:我们假设,在对聚乙二醇干扰素和利巴韦林无反应的人免疫缺陷病毒和丙型肝炎病毒(HIV / HCV)合并感染的患者中,采用聚乙二醇干扰素的维持疗法可以诱导纤维化消退。方法:这是一个随机研究,分为两个平行组。 HIV / HCV合并感染的患者接受聚乙二醇干扰素α-2a的剂量为180μg/周,或继续观察96周。主要终点是在最初和最终的肝活检之间Metavir纤维化评分降低至少一个点的患者百分比。次要终点包括第96周时的血浆纤维化标志物,HCV相关并发症的发生以及生存期。结果:总共52例患者被随机分组​​(聚乙二醇干扰素:25;对照组:27),其中18例患有肝硬化。中位年龄(四分位间距)为44(40-46)岁,男性为69%。共有64%的ALT水平> 1.5正常值,CD4细胞计数为391(296-537)细胞/ mm3; 67%的患者入院时HIV RNA <200copies / mL。主要终点评估了41例患者。聚乙二醇干扰素和对照组的缓解率分别为3/20(15%)和4/21(19%)(p = 0.99)。最终访视时,聚乙二醇干扰素和对照组在血浆纤维化标志物上无显着差异。聚乙二醇干扰素和对照组分别在2和5例患者中观察到严重的肝相关并发症。观察到三例死亡,全部在对照组​​中。结论:在对HCV治疗无反应的HIV / HCV合并感染患者中,使用聚乙二醇干扰素α-2a维持治疗超过96周,并没有改变肝纤维化。 ClinicalTrials.gov标识符:NCT00122616。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号