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本文引用的文献

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Life expectancy after 2015 of adults with HIV on long-term antiretroviral therapy in Europe and North America: a collaborative analysis of cohort studies.2015 年后在欧洲和北美接受长期抗逆转录病毒治疗的艾滋病毒感染者的预期寿命:队列研究的协作分析。
Lancet HIV. 2023 May;10(5):e295-e307. doi: 10.1016/S2352-3018(23)00028-0. Epub 2023 Mar 20.
2
HIV treatment with dolutegravir and doravirine: rationale for selection and clinical outcomes in a highly treatment experienced population.多替拉韦和多拉韦林治疗 HIV:在高度治疗经验人群中选择和临床结局的理由。
Int J STD AIDS. 2022 Oct;33(12):1073-1077. doi: 10.1177/09564624221116533. Epub 2022 Sep 16.
3
Brief Report: Evaluation of Inflammation and Atherogenesis Biomarkers Through 148 Weeks Postswitch to Dolutegravir and Rilpivirine in SWORD-1/SWORD-2.简要报告:SWORD-1/SWORD-2 研究中换用多替拉韦利匹韦林治疗 148 周时炎症和动脉粥样硬化生物标志物的评估。
J Acquir Immune Defic Syndr. 2022 Sep 1;91(1):73-78. doi: 10.1097/QAI.0000000000003019. Epub 2022 May 11.
4
Real life use of dolutegravir doravirine dual regimen in experienced elderly PLWH with multiple comorbidities and on polypharmacy: A retrospective analysis.真实世界中,在具有多种合并症和多种药物治疗的经验丰富的老年 HIV 感染者中使用多替拉韦/多拉韦林双药方案:一项回顾性分析。
Medicine (Baltimore). 2021 Dec 30;100(52):e28488. doi: 10.1097/MD.0000000000028488.
5
Five Years With Dolutegravir Plus Lamivudine as a Switch Strategy: Much More Than a Positive Finding.五年多替拉依(含多替拉韦和拉米夫定)作为一种转换策略:不仅仅是一个积极的发现。
J Acquir Immune Defic Syndr. 2021 Nov 1;88(3):234-237. doi: 10.1097/QAI.0000000000002787.
6
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.多伟拉韦与利托那韦增强的达芦那韦在初治 HIV-1 成人患者中的比较(DRIVE-FORWARD):一项随机、双盲、非劣效性、3 期临床试验的 96 周结果。
Lancet HIV. 2020 Jan;7(1):e16-e26. doi: 10.1016/S2352-3018(19)30336-4. Epub 2019 Nov 15.
7
Switching to Doravirine/Lamivudine/Tenofovir Disoproxil Fumarate (DOR/3TC/TDF) Maintains HIV-1 Virologic Suppression Through 48 Weeks: Results of the DRIVE-SHIFT Trial.切换至多伟拉韦/拉米夫定/富马酸替诺福韦二吡呋酯(DOR/3TC/TDF)治疗 48 周维持 HIV-1 病毒学抑制:DRIVE-SHIFT 试验结果。
J Acquir Immune Defic Syndr. 2019 Aug 1;81(4):463-472. doi: 10.1097/QAI.0000000000002056.
8
Prevalence of predicted resistance to doravirine in HIV-1-positive patients after exposure to non-nucleoside reverse transcriptase inhibitors.非核苷类逆转录酶抑制剂暴露后 HIV-1 阳性患者对多替拉韦耐药的预测率。
Int J Antimicrob Agents. 2019 Apr;53(4):515-519. doi: 10.1016/j.ijantimicag.2019.02.007. Epub 2019 Feb 12.
9
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.多伟拉韦/拉米夫定/替诺福韦酯富马酸与依非韦伦/恩曲他滨/替诺福韦酯富马酸治疗人类免疫缺陷病毒 1 感染初治成人的非劣效性:DRIVE-AHEAD 试验的第 48 周结果。
Clin Infect Dis. 2019 Feb 1;68(4):535-544. doi: 10.1093/cid/ciy540.
10
The Effect of Food on Doravirine Bioavailability: Results from Two Pharmacokinetic Studies in Healthy Subjects.食物对多韦拉韦生物利用度的影响:两项健康受试者药代动力学研究的结果。
Clin Drug Investig. 2017 Jun;37(6):571-579. doi: 10.1007/s40261-017-0512-5.

多替拉韦/度鲁特韦方案:一种替代抗逆转录病毒的 2 药方案,包含多替拉韦和度鲁特韦。

The DoDo experience: an alternative antiretroviral 2-drug regimen of doravirine and dolutegravir.

机构信息

Klinik für Dermatologie und Venerologie, Universitätsklinikum Essen, Hufelandstrasse 55, 45122, Essen, Germany.

Universitätsklinik für Dermatologie, Medizinische Universität Wien, Währinger Gürtel 18-20, 1090, Vienna, Austria.

出版信息

Infection. 2023 Dec;51(6):1823-1829. doi: 10.1007/s15010-023-02075-y. Epub 2023 Aug 1.

DOI:10.1007/s15010-023-02075-y
PMID:37526898
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10665222/
Abstract

BACKGROUND

Currently available antiretroviral 2-drug regimen (2DR) fixed dose combinations may not be suitable for specific situations including the presence of resistance associated mutations (RAM) or drug - drug interactions (DDI). The data on the use of the non-nucleoside reverse transcriptase inhibitor doravirine (DOR) and the integrase inhibitor dolutegravir (DTG) as an alternative 2DR remain scarce.

METHODS

People living with HIV with DOR + DTG as a 2DR are being followed in a prospective observational study.

RESULTS

This analysis describes 85 participants with a median age of 57 years. Median CD4-nadir was 173/µl and a majority (66%) had a history of HIV-associated or AIDS-defining conditions. Antiretroviral history was mostly extensive, and documentation of RAM was frequent. The main reasons for choosing DOR + DTG were DDI (29%), tolerability (25%), and cardiovascular risk reduction (21%). Plasma viral load at switch was < 50 copies/ml in all but 3 instances, median CD4 count was 600/µl. DOR + DTG was later changed to another regimen in 10 participants after a median of 265 days, the other 75 participants have remained on DOR + DTG for a median of 947 days.

CONCLUSION

DOR + DTG as a 2DR proved to be a durable treatment option even in extensively pretreated individuals.

摘要

背景

目前可用的抗逆转录病毒 2 药固定剂量复方可能并不适合某些特定情况,包括存在耐药相关突变(RAM)或药物相互作用(DDI)。关于使用非核苷类逆转录酶抑制剂地拉韦啶(DOR)和整合酶抑制剂多替拉韦(DTG)作为替代 2DR 的数据仍然很少。

方法

正在前瞻性观察研究中对使用 DOR+DTG 作为 2DR 的 HIV 感染者进行随访。

结果

该分析描述了 85 名中位年龄为 57 岁的参与者。中位 CD4 计数最低点为 173/µl,大多数(66%)有 HIV 相关或 AIDS 定义性疾病的病史。抗逆转录病毒治疗史主要广泛,并且经常记录 RAM。选择 DOR+DTG 的主要原因是 DDI(29%)、耐受性(25%)和降低心血管风险(21%)。除 3 例外,所有患者在转换时的血浆病毒载量均<50 拷贝/ml,中位 CD4 计数为 600/µl。在中位 265 天后,有 10 名患者将 DOR+DTG 更换为另一种方案,其余 75 名患者中位持续使用 DOR+DTG 947 天。

结论

即使在广泛预处理的个体中,DOR+DTG 作为 2DR 也被证明是一种持久的治疗选择。