• 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

Stavudine plus lamivudine in advanced human immunodeficiency virus disease: a short-term pilot study.

作者信息

Rouleau D, Conway B, Raboud J, Rae S, Fransen S, Shillington A, Zala C, O'Shaughnessy M V, Montaner J S

机构信息

British Columbia Centre for Excellence in HIV/AIDS, and Canadian HIV Trials Network, St. Paul's Hospital, University of British Columbia, Vancouver.

出版信息

J Infect Dis. 1997 Nov;176(5):1156-60. doi: 10.1086/514107.

DOI:10.1086/514107
PMID:9359713
Abstract

The short-term effects of stavudine (d4T) plus lamivudine (3TC) were evaluated among 48 human immunodeficiency virus-infected patients for whom zidovudine therapy had failed or who could not tolerate zidovudine. Patients were followed for 8 weeks after initiation of open-label d4T plus 3TC. Four patients discontinued therapy, because of neutropenia (1), hepatitis (1), or neuropathy (2). Reduction in virus load was -0.86 (+0.3 to -3.4) log10 copies/mL and CD4 cell increase was 30 (-100 to +290) cells/mm3. Virologic response was associated with a higher CD4 cell count, no prior exposure to d4T and 3TC, and no previous AIDS-defining illness. Virus load reduction for patients naive to 3TC and d4T was -1.47 (-0.14 to -3.37) log10 copies/mL. Short-term use of d4T plus 3TC is safe, well-tolerated, and associated with virologic and substantial immunologic benefits. Further evaluation of d4T and 3TC in combination is warranted.

摘要

相似文献

1
Stavudine plus lamivudine in advanced human immunodeficiency virus disease: a short-term pilot study.
J Infect Dis. 1997 Nov;176(5):1156-60. doi: 10.1086/514107.
2
An open randomized controlled trial of zidovudine plus lamivudine versus stavudine plus lamivudine.齐多夫定加拉米夫定与司他夫定加拉米夫定的开放性随机对照试验。
AIDS. 1998 Aug 20;12(12):1513-9. doi: 10.1097/00002030-199812000-00014.
3
A phase II randomized study of the virologic and immunologic effect of zidovudine + stavudine versus stavudine alone and zidovudine + lamivudine in patients with >300 CD4 cells who were antiretroviral naive (ACTG 298).
AIDS Res Hum Retroviruses. 2002 Jul 1;18(10):699-704. doi: 10.1089/088922202760072311.
4
Lamivudine in combination with zidovudine, stavudine, or didanosine in patients with HIV-1 infection. A randomized, double-blind, placebo-controlled trial. National Institute of Allergy and Infectious Disease AIDS Clinical Trials Group Protocol 306 Investigators.拉米夫定联合齐多夫定、司他夫定或去羟肌苷治疗HIV-1感染患者。一项随机、双盲、安慰剂对照试验。美国国立过敏与传染病研究所艾滋病临床试验组方案306研究人员。
AIDS. 1999 Apr 16;13(6):685-94. doi: 10.1097/00002030-199904160-00009.
5
Safety and efficacy of a simplified fixed-dose combination of stavudine, lamivudine and nevirapine (GPO-VIR) for the treatment of advanced HIV-infected patients: a 24-week study.司他夫定、拉米夫定和奈韦拉平简化固定剂量组合(GPO-VIR)治疗晚期HIV感染患者的安全性和有效性:一项为期24周的研究。
J Med Assoc Thai. 2004 Jul;87(7):760-7.
6
Stavudine, nevirapine and ritonavir in stable antiretroviral therapy-experienced children with human immunodeficiency virus infection.司他夫定、奈韦拉平和利托那韦用于接受稳定抗逆转录病毒治疗的有人类免疫缺陷病毒感染经验的儿童。
Pediatr Infect Dis J. 2002 Feb;21(2):119-25. doi: 10.1097/00006454-200202000-00007.
7
Results of the ALBI trial: a randomized comparison of stavudine/didanosine, zidovudine/lamivudine and alternating treatment in antiretroviral-naive patients.ALBI试验结果:对初治抗逆转录病毒治疗患者中司他夫定/去羟肌苷、齐多夫定/拉米夫定及交替治疗的随机对照比较
Antivir Ther. 1999;4 Suppl 3:71-4.
8
Pilot study of hydroxyurea in human immunodeficiency virus-infected children receiving didanosine and/or stavudine.
Pediatr Infect Dis J. 2000 Nov;19(11):1083-6. doi: 10.1097/00006454-200011000-00011.
9
Experience with the use of a first-line regimen of stavudine, lamivudine and nevirapine in patients in the TREAT Asia HIV Observational Database.在“亚洲治疗艾滋病观察数据库”患者中使用司他夫定、拉米夫定和奈韦拉平一线治疗方案的经验。
HIV Med. 2007 Jan;8(1):8-16. doi: 10.1111/j.1468-1293.2007.00417.x.
10
AVANTI 2. Randomized, double-blind trial to evaluate the efficacy and safety of zidovudine plus lamivudine versus zidovudine plus lamivudine plus indinavir in HIV-infected antiretroviral-naive patients.阿凡提2. 一项随机、双盲试验,旨在评估齐多夫定加拉米夫定与齐多夫定加拉米夫定加茚地那韦在未接受过抗逆转录病毒治疗的HIV感染患者中的疗效和安全性。
AIDS. 2000 Mar 10;14(4):367-74.

引用本文的文献

1
A multiple drug interaction study of stavudine with agents for opportunistic infections in human immunodeficiency virus-infected patients.司他夫定与人类免疫缺陷病毒感染患者机会性感染治疗药物的多重药物相互作用研究。
Antimicrob Agents Chemother. 1999 Mar;43(3):647-50. doi: 10.1128/AAC.43.3.647.
2
Comparison of costs of strategies for measuring levels of human immunodeficiency virus type 1 RNA in plasma by using Amplicor and Ultra Direct assays.使用Amplicor和Ultra Direct检测法测定血浆中1型人类免疫缺陷病毒RNA水平的策略成本比较。
J Clin Microbiol. 1998 Nov;36(11):3369-71. doi: 10.1128/JCM.36.11.3369-3371.1998.