首页> 美国卫生研究院文献>Clinical Infectious Diseases: An Official Publication of the Infectious Diseases Society of America >SWIFT: Prospective 48-Week Study to Evaluate Efficacy and Safety of Switching to Emtricitabine/Tenofovir From Lamivudine/Abacavir in Virologically Suppressed HIV-1 Infected Patients on a Boosted Protease Inhibitor Containing Antiretroviral Regimen
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SWIFT: Prospective 48-Week Study to Evaluate Efficacy and Safety of Switching to Emtricitabine/Tenofovir From Lamivudine/Abacavir in Virologically Suppressed HIV-1 Infected Patients on a Boosted Protease Inhibitor Containing Antiretroviral Regimen

机译:SWIFT:前瞻性48周研究评估了在病毒学抑制的HIV-1感染患者中使用抗逆转录病毒疗法增强的蛋白酶抑制剂后从拉米夫定/依巴韦星转用恩曲他滨/替诺福韦的疗效和安全性

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摘要

>Background. In the United States, emtricitabine/tenofovir disoproxil fumarate (FTC/TDF) is a preferred nucleoside reverse transcriptase inhibitor (NRTI) backbone with lamivudine/abacavir (3TC/ABC) as a commonly used alternative. For patients infected with human immunodeficiency virus (HIV-1) virologically suppressed on a boosted protease inhibitor (PI) + 3TC/ABC regimen, the merits of switching to FTC/TDF as the NRTI backbone are unknown.>Methods. SWIFT was a prospective, randomized, open-label 48-week study to evaluate efficacy and safety of switching to FTC/TDF. Subjects receiving 3TC/ABC + PI + ritonavir (RTV) with HIV-1 RNA < 200 c/mL ≥3 months were randomized to continue 3TC/ABC or switch to FTC/TDF. The primary endpoint was time to loss of virologic response (TLOVR) with noninferiority measured by delta of 12%. Virologic failure (VF) was defined as confirmed rebound or the last HIV-1 RNA measurement on study drug ≥200 c/mL.>Results. In total, 311 subjects were treated in this study (155 to PI + RTV + FTC/TDF, 156 to PI + RTV + 3TC/ABC). Baseline characteristics were similar between the arms: 85% male, 28% black, median age, 46 years; and median CD4 532 cells/mm3. By TLOVR through week 48, switching to FTC/TDF was noninferior compared to continued 3TC/ABC (86.4% vs 83.3%, treatment difference 3.0% (95% confidence interval, −5.1% to 11.2%). Fewer subjects on FTC/TDF experienced VF (3 vs 11; P = .034). FTC/TDF showed greater declines in fasting low-density lipoproteins (LDL), total cholesterol (TC), and triglycerides (TG) with significant declines in LDL and TC beginning at week 12 with no TC/HDL ratio change. Switching to FTC/TDF showed improved NCEP thresholds for TC and TG and improved 10-year Framingham TC calculated scores. Decreased epidermal growth factor receptor (eGFR) was observed in both arms with a larger decrease in the FTC/TDF arm.>Conclusions. Switching to FTC/TDF from 3TC/ABC maintained virologic suppression, had fewer VFs, improved lipid parameters and Framingham scores but decreased eGFR.>ClinicalTrials.gov identifier. .
机译:>背景。在美国,恩曲他滨/替诺福韦富马酸替诺福韦(FTC / TDF)是首选的核苷逆转录酶抑制剂(NRTI)骨架,而拉米夫定/阿巴卡韦(3TC / ABC)是常用替代品。对于通过增强蛋白酶抑制剂(PI)+ 3TC / ABC方案在病毒学上受到抑制的人类免疫缺陷病毒(HIV-1)感染的患者,改用FTC / TDF作为NRTI骨架的优点尚不清楚。>方法。 strong> SWIFT是一项前瞻性,随机,开放标签的48周研究,旨在评估转用FTC / TDF的有效性和安全性。接受3TC / ABC + PI +利托那韦(RTV)且HIV-1 RNA <200 c / mL≥3个月的受试者被随机分配以继续3TC / ABC或改用FTC / TDF。主要终点是达到病毒学应答丧失(TLOVR)的时间,非劣效性的差异为12%。病毒学衰竭(VF)定义为对研究药物≥200c / mL的确诊反弹或最后一次HIV-1 RNA测定。>结果。本研究总共治疗了311名受试者(155名PI + RTV + FTC / TDF,156至PI + RTV + 3TC / ABC)。两臂的基线特征相似:男性85%,黑人28%,中位年龄46岁;和中值CD4 532细胞/ mm 3 。通过TLOVR到第48周,与继续使用3TC / ABC相比,转换为FTC / TDF的效果不差(86.4%vs 83.3%,治疗差异3.0%(95%置信区间,-5.1%至11.2%)。有经验的VF(3比11; P = .034)FTC / TDF显示空腹低密度脂蛋白(LDL),总胆固醇(TC)和甘油三酸酯(TG)下降幅度更大,LDL和TC从周开始显着下降12,TC / HDL比例无变化,改用FTC / TDF显示TC和TG的NCEP阈值得到改善,Framingham TC计算的10年分数得到改善;两臂的表皮生长因子受体(eGFR)均下降,且TC / HDL下降幅度更大>结论。从3TC / ABC切换到FTC / TDF可以保持病毒学抑制作用,VF减少,脂质参数和Framingham评分降低,但eGFR降低。> ClinicalTrials.gov标识符。

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