• 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

DOLAMA 200:西班牙治疗经验丰富的 HIV-1 感染者中,度鲁特韦加拉米夫定双药治疗的有效性和安全性。

DOLAMA 200: Effectiveness and Safety of a Dual Therapy with Dolutegravir Plus Lamivudine in Treatment-Experienced HIV-1 Infected Real World Participants in Spain.

机构信息

Unit of Infectious Diseases, Instituto de Investigación Biosanitario de Granada (IBS-Granada), Virgen de las Nieves University Hospital, 18014 Granada, Spain.

Department of Infectious Diseases, Virgen del Rocio University Hospitals, 41013 Seville, Spain.

出版信息

Viruses. 2024 Feb 6;16(2):259. doi: 10.3390/v16020259.

DOI:10.3390/v16020259
PMID:38400035
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10893067/
Abstract

The continuous pharmacological advances in antiretroviral treatment (ART) and the increasing understanding of HIV drug resistance has led to a change in the paradigm of ART optimization in the setting of the viral suppression of treatment-experienced patients with the emerging evidence of the effectiveness and safety of dual therapies. The aim of this study is to determine the antiviral efficacy and safety of switching to Dolutegravir + Lamivudine in people living with HIV, and to analyze the rate of patients with virologic failure (VF). A total of 200 patients were included with a median age of 51 years, 189 cells/µL of nadir CD4+, 13 years on ART and four previous ART regimens. Among the 168 patients who completed a follow-up at 48 weeks, a total of five VFs occurred, resulting in a 2.98% (5/168) VF rate. The results of the intention-to-treat analysis were a VF rate of 2.54% (5/197), and the rate of patients/year with viral suppression was 98.3% (298/303) in the observed data analysis. We observed a significant improvement in mean CD4 lymphocytes, the CD4/CD8 ratio and lipid profiles. The optimization of ART to DTG plus 3TC is a cost-effective switch option for treatment-experienced HIV patients, and also improves their lipid profiles.

摘要

抗逆转录病毒治疗(ART)的不断药理学进展以及对 HIV 耐药性的不断深入了解,导致在治疗经验丰富的患者病毒抑制的背景下,对 ART 优化的范例发生了变化,出现了双重疗法有效性和安全性的新兴证据。本研究旨在确定将 Dolutegravir + Lamivudine 转换为治疗 HIV 感染者的抗病毒疗效和安全性,并分析病毒学失败(VF)患者的比率。共纳入 200 名患者,中位年龄为 51 岁,CD4+ 最低点为 189 个细胞/µL,接受 ART 治疗 13 年,接受了 4 种以前的 ART 方案。在完成 48 周随访的 168 名患者中,共有 5 例发生 VF,VF 发生率为 2.98%(5/168)。意向治疗分析的结果为 VF 发生率为 2.54%(5/197),在观察数据分析中,病毒抑制的患者/年比率为 98.3%(298/303)。我们观察到 CD4 淋巴细胞、CD4/CD8 比值和血脂谱的平均水平显著改善。将 ART 优化为 DTG 加 3TC 是一种针对治疗经验丰富的 HIV 患者具有成本效益的转换选择,并且还改善了他们的血脂谱。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/491a/10893067/d0f7974af6d1/viruses-16-00259-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/491a/10893067/6bab69f8530f/viruses-16-00259-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/491a/10893067/d0f7974af6d1/viruses-16-00259-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/491a/10893067/6bab69f8530f/viruses-16-00259-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/491a/10893067/d0f7974af6d1/viruses-16-00259-g002.jpg

相似文献

1
DOLAMA 200: Effectiveness and Safety of a Dual Therapy with Dolutegravir Plus Lamivudine in Treatment-Experienced HIV-1 Infected Real World Participants in Spain.DOLAMA 200:西班牙治疗经验丰富的 HIV-1 感染者中,度鲁特韦加拉米夫定双药治疗的有效性和安全性。
Viruses. 2024 Feb 6;16(2):259. doi: 10.3390/v16020259.
2
DOLAMA study: Effectiveness, safety and pharmacoeconomic analysis of dual therapy with dolutegravir and lamivudine in virologically suppressed HIV-1 patients.多拉米双药联合治疗研究:多替拉韦与拉米夫定联合治疗对病毒学抑制的HIV-1患者的有效性、安全性及药物经济学分析
Medicine (Baltimore). 2019 Aug;98(32):e16813. doi: 10.1097/MD.0000000000016813.
3
Efficacy and safety of switching to dolutegravir plus lamivudine versus continuing triple antiretroviral therapy in virologically suppressed adults with HIV at 48 weeks (DOLAM): a randomised non-inferiority trial.在 48 周时对病毒学抑制的 HIV 成人切换至多替拉韦加拉米夫定加恩曲他滨与继续三联抗逆转录病毒治疗相比的疗效和安全性(DOLAM):一项随机非劣效性试验。
Lancet HIV. 2021 Aug;8(8):e463-e473. doi: 10.1016/S2352-3018(21)00100-4.
4
Dolutegravir Plus Lamivudine as Initial Therapy for HIV-1 Infected and ARV-naïve Patients in West China, 24-Weeks Results of a Preliminary Real-world Study.多替拉韦加拉米夫定作为初始治疗方案用于中国西部 HIV-1 感染且未接受过 ARV 治疗的患者:一项初步真实世界研究的 24 周结果。
Curr HIV Res. 2022;20(3):222-227. doi: 10.2174/1570162X20666220514165728.
5
Efficacy and safety of switching to dolutegravir/lamivudine in virologically suppressed people with HIV-1 aged ≥ 50 years: week 48 pooled results from the TANGO and SALSA studies.在病毒学抑制的 HIV-1 年龄≥50 岁的人群中,转换为多替拉韦/拉米夫定的疗效和安全性:来自 TANGO 和 SALSA 研究的第 48 周汇总结果。
AIDS Res Ther. 2024 Mar 21;21(1):17. doi: 10.1186/s12981-024-00604-9.
6
Efficacy and tolerability of lamivudine plus dolutegravir compared with lamivudine plus boosted PIs in HIV-1 positive individuals with virologic suppression: a retrospective study from the clinical practice.拉米夫定联合度鲁特韦与拉米夫定联合增效蛋白酶抑制剂治疗病毒学抑制的 HIV-1 阳性个体的疗效和耐受性:一项来自临床实践的回顾性研究。
BMC Infect Dis. 2019 Jan 17;19(1):59. doi: 10.1186/s12879-018-3666-8.
7
Effectiveness, Weight Changes, and Metabolic Outcomes on Switch to Generic Dolutegravir/Lamivudine Among People with HIV in Western India: An Observational Study.在西印度,观察性研究:转换为通用多替拉韦/拉米夫定对 HIV 感染者的有效性、体重变化和代谢结局。
AIDS Res Hum Retroviruses. 2024 Apr;40(4):204-215. doi: 10.1089/AID.2022.0167. Epub 2024 Jan 5.
8
Long-term outcome of lamivudine/dolutegravir dual therapy in HIV-infected, virologically suppressed patients.拉米夫定/多替拉韦双药治疗病毒学抑制的 HIV 感染者的长期结局。
BMC Infect Dis. 2022 Oct 12;22(1):782. doi: 10.1186/s12879-022-07769-6.
9
Efficacy and Safety of Switching to Dolutegravir/Lamivudine in Virologically Suppressed People Living with HIV-1 Aged Over 65 Years.在年龄超过 65 岁的 HIV-1 感染者中,转换为多替拉韦/拉米夫定的疗效和安全性。
AIDS Res Hum Retroviruses. 2024 Feb;40(2):73-79. doi: 10.1089/AID.2023.0046. Epub 2023 Jul 5.
10
Efficacy and Safety of Switching to Dolutegravir/Lamivudine Versus Continuing a Tenofovir Alafenamide-Based 3- or 4-Drug Regimen for Maintenance of Virologic Suppression in Adults Living With Human Immunodeficiency Virus Type 1: Results Through Week 144 From the Phase 3, Noninferiority TANGO Randomized Trial.在成人人类免疫缺陷病毒 1 型感染者中,转换为多替拉韦/拉米夫定与继续使用替诺福韦艾拉酚胺为基础的三或四药物方案维持病毒学抑制的疗效和安全性:来自 3 期非劣效性 TANGO 随机试验的第 144 周结果。
Clin Infect Dis. 2022 Sep 29;75(6):975-986. doi: 10.1093/cid/ciac036.

引用本文的文献

1
Real-World Effectiveness and Tolerability of Dolutegravir and Lamivudine 2-Drug Regimen in People Living with HIV: Systematic Literature Review and Meta-Analysis.多替拉韦与拉米夫定二联疗法在HIV感染者中的真实世界有效性和耐受性:系统文献综述与荟萃分析
Infect Dis Ther. 2025 Feb;14(2):357-383. doi: 10.1007/s40121-024-01103-0. Epub 2025 Jan 18.
2
Efficacy and Tollerability of INI-Based 2-Drug Regimen in Virosuppressed Persons Living with HIV: A Systematic Review and Meta-Analysis.基于整合酶抑制剂的双药方案对病毒抑制的HIV感染者的疗效和耐受性:一项系统评价和荟萃分析
Infect Chemother. 2024 Sep;56(3):395-405. doi: 10.3947/ic.2024.0066.

本文引用的文献

1
Rildo: Real-World Multicenter Study on the Effectiveness and Safety of Single-Tablet Regimen of Dolutegravir plus Rilpivirine in Treatment-Experienced People Living with HIV.里尔多:多替拉韦/利匹韦林单片复方制剂在治疗经验丰富的 HIV 感染者中的有效性和安全性的真实世界多中心研究。
Viruses. 2022 Nov 25;14(12):2626. doi: 10.3390/v14122626.
2
Viro-Immunological, Clinical Outcomes and Costs of Switching to BIC/TAF/FTC in a Cohort of People Living with HIV: A 48-Week Prospective Analysis.一组HIV感染者改用比克替拉韦/替诺福韦艾拉酚胺/恩曲他滨的病毒免疫、临床结局及成本:一项48周的前瞻性分析
Biomedicines. 2022 Jul 28;10(8):1823. doi: 10.3390/biomedicines10081823.
3
DOLAVI Real-Life Study of Dolutegravir Plus Lamivudine in Naive HIV-1 Patients (48 Weeks).
多替拉韦真实世界研究:初治 HIV-1 患者中多替拉韦联合拉米夫定(48 周)。
Viruses. 2022 Mar 4;14(3):524. doi: 10.3390/v14030524.
4
Efficacy and Safety of Switching to the 2-Drug Regimen Dolutegravir/Lamivudine Versus Continuing a 3- or 4-Drug Regimen for Maintaining Virologic Suppression in Adults Living With Human Immunodeficiency Virus 1 (HIV-1): Week 48 Results From the Phase 3, Noninferiority SALSA Randomized Trial.在成人人类免疫缺陷病毒 1(HIV-1)感染者中,转换为二药方案多替拉韦/拉米夫定与继续三药或四药方案维持病毒学抑制的疗效和安全性:来自 III 期非劣效性 SALSA 随机试验的第 48 周结果。
Clin Infect Dis. 2023 Feb 18;76(4):720-729. doi: 10.1093/cid/ciac130.
5
Dolutegravir/lamivudine as a first-line regimen in a test-and-treat setting for newly diagnosed people living with HIV.多替拉韦/拉米夫定作为新诊断的 HIV 感染者一线治疗方案。
AIDS. 2021 Oct 1;35(12):1957-1965. doi: 10.1097/QAD.0000000000002979.
6
Dolutegravir Plus Lamivudine Two-Drug Regimen: Safety, Efficacy and Diagnostic Considerations for Its Use in Real-Life Clinical Practice-A Refined Approach in the COVID-19 Era.多替拉韦加拉米夫定双药方案:在实际临床实践中使用的安全性、有效性及诊断考量——COVID-19 时代的一种优化方法
Diagnostics (Basel). 2021 Apr 29;11(5):809. doi: 10.3390/diagnostics11050809.
7
Efficacy and Safety of Switching to Dolutegravir With Boosted Darunavir in Virologically Suppressed Adults With HIV-1: A Randomized, Open-Label, Multicenter, Phase 3, Noninferiority Trial: The DUALIS Study.在病毒学抑制的成人HIV-1感染者中换用多替拉韦联合增强型达芦那韦的疗效和安全性:一项随机、开放标签、多中心、3期、非劣效性试验:DUALIS研究
Open Forum Infect Dis. 2020 Aug 13;7(9):ofaa356. doi: 10.1093/ofid/ofaa356. eCollection 2020 Sep.
8
Efficacy and Safety of Switching to Dolutegravir/Lamivudine Fixed-Dose 2-Drug Regimen vs Continuing a Tenofovir Alafenamide-Based 3- or 4-Drug Regimen for Maintenance of Virologic Suppression in Adults Living With Human Immunodeficiency Virus Type 1: Phase 3, Randomized, Noninferiority TANGO Study.替诺福韦艾拉酚胺/拉米夫定固定剂量 2 药方案与继续使用基于替诺福韦艾拉酚胺的 3 或 4 药方案治疗维持人类免疫缺陷病毒 1 型感染者病毒学抑制的疗效和安全性:3 期、随机、非劣效 TANGO 研究。
Clin Infect Dis. 2020 Nov 5;71(8):1920-1929. doi: 10.1093/cid/ciz1243.
9
DOLAMA study: Effectiveness, safety and pharmacoeconomic analysis of dual therapy with dolutegravir and lamivudine in virologically suppressed HIV-1 patients.多拉米双药联合治疗研究:多替拉韦与拉米夫定联合治疗对病毒学抑制的HIV-1患者的有效性、安全性及药物经济学分析
Medicine (Baltimore). 2019 Aug;98(32):e16813. doi: 10.1097/MD.0000000000016813.
10
Efficacy and safety of dolutegravir-rilpivirine for maintenance of virological suppression in adults with HIV-1: 100-week data from the randomised, open-label, phase 3 SWORD-1 and SWORD-2 studies.多替拉韦利匹韦林用于维持 HIV-1 成人感染者病毒学抑制的疗效和安全性:来自随机、开放标签、III 期 SWORD-1 和 SWORD-2 研究的 100 周数据。
Lancet HIV. 2019 Sep;6(9):e576-e587. doi: 10.1016/S2352-3018(19)30149-3. Epub 2019 Jul 12.