Switching to the single-tablet regimen of elvitegravir, cobicistat, emtricitabine, and tenofovir DF from non-nucleoside reverse transcriptase inhibitor plus coformulated emtricitabine and tenofovir DF regimens: Week 96 results of STRATEGY-NNRTI.

Q2 Medicine
HIV Clinical Trials Pub Date : 2017-07-01 Epub Date: 2017-07-09 DOI:10.1080/15284336.2017.1338844
Anton Pozniak, Jason Flamm, Andrea Antinori, Mark Bloch, Douglas Ward, Juan Berenguer, Pierre Cote, Kristen Andreatta, William Garner, Javier Szwarcberg, Thai Nguyen-Cleary, Damian J McColl, David Piontkowsky
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引用次数: 16

Abstract

Background: HIV-1-infected, virologically suppressed adults wanting to simplify or change their non-nucleoside reverse transcriptase inhibitor (NNRTI)-based regimens may benefit from switching to the single-tablet regimen of elvitegravir, cobicistat, emtricitabine, and tenofovir disoproxil fumarate (E/C/F/TDF).

Objective: We examined differences in the proportion of participants with HIV-1 RNA < 50 copies/mL (Snapshot analysis), change in CD4 cell count, safety, and patient-reported outcomes in participants switching to E/C/F/TDF from an NNRTI + FTC/TDF (TVD) regimen.

Methods: STRATEGY-NNRTI was a 96-week, phase 3b, randomized, open-label, study examining the efficacy, safety, and tolerability of switching to E/C/F/TDF in virologically suppressed individuals (HIV-1 RNA < 50 copies/mL) on an NNRTI + TVD regimen. Participants were randomized to switch or remain on their NNRTI-based regimen (no-switch).

Results: At Week 96, 87% (251/290) of switch and 80% (115/143) of no-switch participants maintained HIV-1 RNA < 50 copies/mL (difference 6.1%; 95% CI -1.3 to 14.2%; p = 0.12) according to the FDA-defined snapshot algorithm. Both groups had similar proportions of subjects with virologic failure (2.8% switch, 1.4% no-switch). Discontinuations resulting from adverse events were infrequent (3% [9/291] switch, 2% [3/143] no-switch). Three switch participants (1%) discontinued due to renal adverse events (2 of the 3 before Week 48). Switch participants reported significant improvements in neuropsychiatric symptoms by as early as Week 4, and which were maintained through Week 96.

Conclusions: E/C/F/TDF is safe and effective and reduces NNRTI-associated neuropsychiatric symptoms for virologically suppressed HIV-positive adults switching from an NNRTI plus FTC/TDF-based regimen.

从非核苷类逆转录酶抑制剂加复方恩曲他滨和替诺福韦DF方案切换到依维替韦、可比司他、恩曲他滨和替诺福韦DF单片方案:STRATEGY-NNRTI第96周结果
背景:hiv -1感染、病毒学抑制的成年人想要简化或改变他们的非核苷逆转录酶抑制剂(NNRTI)为基础的方案,可能会受益于切换到依维替韦、可比司他、恩曲他滨和富马酸替诺福韦二氧吡酯(E/C/F/TDF)的单片方案。方法:STRATEGY-NNRTI是一项为期96周、随机、开放标签的3b期研究,旨在检测在病毒学抑制个体(HIV-1 RNA)中切换到E/C/F/TDF的有效性、安全性和耐受性。结果:在第96周,87%(251/290)的切换参与者和80%(115/143)的未切换参与者维持HIV-1 RNA。E/C/F/TDF是安全有效的,对于从NNRTI + FTC/TDF为基础的方案转换为病毒学抑制的hiv阳性成人,可减少NNRTI相关的神经精神症状。
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来源期刊
HIV Clinical Trials
HIV Clinical Trials 医学-传染病学
CiteScore
1.76
自引率
0.00%
发文量
0
审稿时长
>12 weeks
期刊介绍: HIV Clinical Trials is devoted exclusively to presenting information on the latest developments in HIV/AIDS clinical research. This journal enables readers to obtain the most up-to-date, innovative research from around the world.
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