DORA:从基于多鲁曲韦或依非韦伦的一线抗逆转录病毒疗法转向基于多拉韦林的一线抗逆转录病毒疗法的 IIIb 期转换研究中,感染艾滋病病毒的黑人妇女 48 周的体重和代谢变化。

IF 2.8 3区 医学 Q2 INFECTIOUS DISEASES
HIV Medicine Pub Date : 2024-09-17 DOI:10.1111/hiv.13711
Joana Woods, Simiso Sokhela, Godspower Akpomiemie, Bronwyn Bosch, Karlien Möller, Esther Bhaskar, Chelsea Kruger, Ncomeka Manentsa, Noxolo Tom, Philadelphia Macholo, Nomathemba Chandiwana, Andrew Hill, Michelle Moorhouse, Willem D F Venter
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引用次数: 0

摘要

目标:抗逆转录病毒整合疗法治疗相关的体重增加和代谢并发症,尤其是在黑人妇女中:以抗逆转录病毒整合酶为基础的治疗方案与治疗相关的体重增加和代谢并发症,尤其是在黑人女性中,表明需要替代选择:我们进行了一项为期 48 周、开放标签、单臂、单中心、IIIb 期转换研究,以评估黑人女性从稳定的依非韦伦或多鲁特韦为主的抗逆转录病毒疗法转换为多拉韦林/拉米夫定/富马酸替诺福韦二吡呋酯疗法的耐受性、安全性和疗效:101 名参与者(中位年龄 35 岁;四分位数间距 31-40 岁)在筛查时正在接受依非韦伦(46 人;平均治疗时间 1.7 年)或基于多拉韦(55 人;平均治疗时间 1.5 年)的抗逆转录病毒治疗。在整个研究过程中,病毒抑制率大于 90%,只有一例多拉韦林耐药(106 M、V108I 和 H221Y 突变)。第 48 周时的平均体重百分比变化为 4.7%(95% 置信区间 [CI] 3.0-6.5;P我们的研究结果表明,黑人女性从依非韦伦或多鲁曲韦转为多拉韦林治疗是安全有效的,血脂状况得到显著改善,但并不能阻止体重的逐渐增加。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
DORA: 48-week weight and metabolic changes in Black women with HIV, in a phase IIIb switch study from dolutegravir- or efavirenz- to doravirine-based first-line antiretroviral therapy.

Objectives: Treatment-related weight gain and metabolic complications with antiretroviral integrase-based regimens, especially among Black women, suggest the need for alternative options.

Methods: We conducted a 48-week, open-label, single-arm, single-centre, phase IIIb switch study to evaluate the tolerability, safety and efficacy of switching from stable efavirenz- or dolutegravir-based antiretroviral therapy to doravirine/lamivudine/tenofovir disoproxil fumarate in Black women.

Results: The 101 participants enrolled (median age 35 years; interquartile range 31-40) were on efavirenz (n = 46; mean duration on therapy 1.7 years) or dolutegravir-based (n = 55; mean duration 1.5 years) antiretrovirals at screening. Retention at 48 weeks was 92/101 participants, and viral suppression was >90% throughout the study, with a single case of doravirine resistance (106 M, V108I and H221Y mutations). The mean weight percentage change at week 48 was 4.7% (95% confidence interval [CI] 3.0-6.5; p < 0.001), and the adjusted mean change was 2.7 kg (95% CI 1.50-3.98; p < 0.001); for efavirenz, the percentage change was 5.0% (95% CI 2.9-7.1; p < 0.001), and the adjusted weight gain was 3.5 kg (95% CI 1.93-5.13); for dolutegravir, the percentage change was 4.5% (95% CI 1.8-7.3; p < 0.001), and the adjusted weight gain was 2.1 kg (95% CI 0.26-3.90). Statistically significant decreases in lipid panel percent mean to week 48 included: total cholesterol -8.4% (95% CI -11.3 to -5.5; p < 0.001), triglycerides -10.4% (95% CI -16.4 to -4.4; p < 0.001) and high-density lipoprotein -14.8% (95% CI -18.5 to -11.2%; p < 0.001), with minor differences when disaggregating the mean percent change in lipids between previous efavirenz/dolutegravir regimens. Adverse events due to doravirine were few and mild.

Conclusions: Our findings suggest that a switch to doravirine from efavirenz or dolutegravir is safe and effective in Black women, with significant improvement in lipid profiles, but does not arrest progressive weight gain.

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来源期刊
HIV Medicine
HIV Medicine 医学-传染病学
CiteScore
5.10
自引率
10.00%
发文量
167
审稿时长
6-12 weeks
期刊介绍: HIV Medicine aims to provide an alternative outlet for publication of international research papers in the field of HIV Medicine, embracing clinical, pharmocological, epidemiological, ethical, preclinical and in vitro studies. In addition, the journal will commission reviews and other feature articles. It will focus on evidence-based medicine as the mainstay of successful management of HIV and AIDS. The journal is specifically aimed at researchers and clinicians with responsibility for treating HIV seropositive patients.
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