文献检索文档翻译深度研究
Suppr Zotero 插件Zotero 插件
邀请有礼套餐&价格历史记录

新学期,新优惠

限时优惠:9月1日-9月22日

30天高级会员仅需29元

1天体验卡首发特惠仅需5.99元

了解详情
不再提醒
插件&应用
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
高级版
套餐订阅购买积分包
AI 工具
文献检索文档翻译深度研究
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 @ 2025

基于多伟拉韦的治疗方案在真实世界中的疗效和安全性:一项前瞻性单中心法国研究。

Efficacy and Safety of Doravirine-Based Regimens in Real Life: A Prospective Monocentric French Study.

机构信息

Service de Virologie et Mycobactériologie, CHU de Poitiers, Poitiers, France.

Laboratoire Inflammation, Tissus Epithéliaux et Cytokines, UR 15560, Université de Poitiers, Poitiers, France.

出版信息

AIDS Res Hum Retroviruses. 2022 Oct;38(10):779-781. doi: 10.1089/AID.2022.0058.


DOI:10.1089/AID.2022.0058
PMID:36097760
Abstract

Doravirine (DOR) efficacy and safety have been evaluated in adult naive or treated patients starting a DOR-based regimen between September 15, 2019, and December 31, 2020. Medical history and examination, laboratory results, and tolerance were assessed during the 48 weeks of follow-up. Among the 77 patients included, virological control (VC) was noticed for 66 patients at baseline. Median age was 51 years, and 62% were men. The most common reason for initiating a DOR-based therapy was toxicity (44; 67%) and, especially, weight gain. A virological suppression (VS) was maintained in 55 (83%) patients of the VC group and noticed in 9 (82%) of the non-VC patients at week 48, by intention-to-treat analysis. On treatment analysis, 98% and 100% patients achieved VS in the VC and non-VC groups, respectively. The renal and metabolic tolerance were good. DOR-based regimens appear to be a safe and relevant strategy to circumvent drug interactions and drugs with a poor metabolic tolerance profile.

摘要

多伟拉韦(DOR)的疗效和安全性已在 2019 年 9 月 15 日至 2020 年 12 月 31 日期间开始接受 DOR 为基础方案治疗的初治或经治成年患者中得到评估。在 48 周的随访期间,评估了患者的病史和检查、实验室结果以及耐受性。在纳入的 77 例患者中,66 例患者在基线时存在病毒学控制(VC)。中位年龄为 51 岁,62%为男性。启动 DOR 为基础治疗的最常见原因是毒性(44 例;67%),尤其是体重增加。在 VC 组中,55 例(83%)患者维持了病毒学抑制(VS),在意向治疗分析中,48 周时,9 例(82%)非 VC 患者也出现了 VS。在治疗分析中,VC 组和非 VC 组分别有 98%和 100%的患者达到了 VS。肾和代谢耐受性良好。DOR 为基础的方案似乎是一种安全且相关的策略,可以规避药物相互作用和代谢耐受性差的药物。

相似文献

[1]
Efficacy and Safety of Doravirine-Based Regimens in Real Life: A Prospective Monocentric French Study.

AIDS Res Hum Retroviruses. 2022-10

[2]
Efficacy and safety of doravirine in treatment-naive HIV-1-infected adults: a systematic review and meta-analysis.

Environ Sci Pollut Res Int. 2021-3

[3]
Doravirine versus ritonavir-boosted darunavir in antiretroviral-naive adults with HIV-1 (DRIVE-FORWARD): 96-week results of a randomised, double-blind, non-inferiority, phase 3 trial.

Lancet HIV. 2019-11-15

[4]
Islatravir in combination with doravirine for treatment-naive adults with HIV-1 infection receiving initial treatment with islatravir, doravirine, and lamivudine: a phase 2b, randomised, double-blind, dose-ranging trial.

Lancet HIV. 2021-6

[5]
Changes in Metabolic Profile in PLWHIV Switching to Doravirine-Based Regimen.

Viruses. 2023-4-25

[6]
Doravirine versus ritonavir-boosted darunavir in antiretroviral-naive adults with HIV-1 (DRIVE-FORWARD): 48-week results of a randomised, double-blind, phase 3, non-inferiority trial.

Lancet HIV. 2018-3-25

[7]
Clinical Pharmacodynamics, Pharmacokinetics, and Drug Interaction Profile of Doravirine.

Clin Pharmacokinet. 2019-12

[8]
Doravirine/Lamivudine/Tenofovir Disoproxil Fumarate (TDF) Versus Efavirenz/Emtricitabine/TDF in Treatment-naive Adults With Human Immunodeficiency Virus Type 1 Infection: Week 96 Results of the Randomized, Double-blind, Phase 3 DRIVE-AHEAD Noninferiority Trial.

Clin Infect Dis. 2021-7-1

[9]
Once-daily Doravirine in Human Immunodeficiency Virus Type 1-Infected, Antiretroviral-naive Adults: An Integrated Efficacy Analysis.

Clin Infect Dis. 2020-3-17

[10]
Doravirine/Lamivudine/Tenofovir Disoproxil Fumarate is Non-inferior to Efavirenz/Emtricitabine/Tenofovir Disoproxil Fumarate in Treatment-naive Adults With Human Immunodeficiency Virus-1 Infection: Week 48 Results of the DRIVE-AHEAD Trial.

Clin Infect Dis. 2019-2-1

引用本文的文献

[1]
Factors influencing antiretroviral therapy switching in people with virologically suppressed HIV-1: a cross-sectional multicenter study in France.

AIDS. 2025-5-1

[2]
Effectiveness and Tolerability of DOR/3TC/TDF in Experienced People with HIV Switching from RPV/FTC/TDF: A Retrospective, Single Center Cohort Study.

Pharmaceuticals (Basel). 2024-12-17

[3]
Weight change with antiretroviral switch from integrase inhibitor or tenofovir alafenamide-based to Doravirine-Based regimens in people with HIV.

HIV Res Clin Pract. 2024-12

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

推荐工具

医学文档翻译智能文献检索