DEFINE: A Prospective, Randomized, Phase 4 Trial to Assess a Protease Inhibitor-based Regimen Switch Strategy to Manage Integrase Inhibitor-related Weight Gain.

IF 8.2 1区 医学 Q1 IMMUNOLOGY Clinical Infectious Diseases Pub Date : 2024-09-04 DOI:10.1093/cid/ciae449
David Anderson, Moti Ramgopal, Debbie P Hagins, Johnnie Lee, Richard Bruce Simonson, Tien-Huei Hsu, Ping Xu, Nina Ahmad, William R Short
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Abstract

Background: Integrase strand transfer inhibitor (InSTI)-based antiretroviral therapies have been associated with greater weight gain in people living with HIV versus on protease inhibitor (PI)-based regimens. The DEFINE study investigated whether switching from an InSTI- to a PI-based regimen could mitigate/reverse weight gain.

Methods: DEFINE (NCT04442737) was a randomized, 48-week, open-label, prospective, phase 4 study in virologically suppressed adults with HIV-1 and ≥10% weight gain on InSTI+tenofovir alafenamide (TAF)/emtricitabine (FTC) (<36 months pre-screening). Participants either switched immediately to darunavir/cobicistat/emtricitabine/TAF (D/C/F/TAF) or continued InSTI+TAF/FTC during Weeks 0-24 then switched to D/C/F/TAF for Weeks 24-48. The primary endpoint was least squares (LS) mean (95% confidence interval [CI]) percent weight change from baseline to Week 24.

Results: Overall, 103 adults were randomized (D/C/F/TAF, n=53; InSTI+TAF/FTC, n=50); 30% female; 61% Black/African American. No significant difference in weight change was observed at Week 24 (LS mean change: D/C/F/TAF, 0.63% [95%CI: -0.44, 1.70] vs InSTI+TAF/FTC, -0.24% [-1.35, 0.87]; p=0.24); however, a trend towards weight loss was observed with extended time post-ARV switch to D/C/F/TAF (baseline to Week 48, -0.36% [-1.77, 1.06]), particularly in subgroups at higher weight gain risk (eg, females, Black/African Americans). Metabolic endpoints paralleled weight change over time. D/C/F/TAF was well tolerated, with comparable virologic efficacy between arms.

Conclusions: While no significant change in body weight was observed at 24 weeks after switching from InSTI+TAF/FTC to D/C/F/TAF among adults with weight gain, a trend towards weight loss emerged with longer time post-ARV switch, supporting further investigation of antiretroviral selection/switch for weight management.

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DEFINE:一项前瞻性、随机、4 期试验,评估基于蛋白酶抑制剂的治疗方案转换策略,以控制整合酶抑制剂相关的体重增加。
背景:以整合酶链转移抑制剂(InSTI)为基础的抗逆转录病毒疗法与以蛋白酶抑制剂(PI)为基础的疗法相比,会导致艾滋病病毒感染者体重增加。DEFINE研究调查了从基于InSTI的疗法转为基于PI的疗法能否减轻/逆转体重增加:DEFINE(NCT04442737)是一项为期48周、开放标签、前瞻性的随机4期研究,研究对象为病毒学抑制的成人HIV-1感染者,他们在接受InSTI+替诺福韦阿拉非酰胺(TAF)/恩曲他滨(FTC)治疗后体重增加≥10%(结果:总共有103名成人接受了随机4期研究(NCT04442737):共有 103 名成人接受了随机治疗(D/C/F/TAF,n=53;InSTI+TAF/FTC,n=50);30% 为女性;61% 为黑人/非裔美国人。第 24 周未观察到体重变化有明显差异(LS 平均变化:D/C/F/TAF,0.63% [95%CI: -0.44, 1.70] vs InSTI+TAF/FTC, -0.24% [-1.35, 0.87];P=0.24);然而,随着ARV转为D/C/F/TAF后时间的延长,观察到体重有下降趋势(基线至第48周,-0.36% [-1.77, 1.06]),尤其是在体重增加风险较高的亚组(如女性、黑人/非裔美国人)。代谢终点与体重随时间变化的情况一致。D/C/F/TAF耐受性良好,两组之间的病毒学疗效相当:虽然在体重增加的成人中,从 InSTI+TAF/FTC 转为 D/C/F/TAF 后 24 周体重没有明显变化,但随着抗逆转录病毒药物转换后时间的延长,出现了体重下降的趋势,这支持进一步研究抗逆转录病毒药物的选择/转换以控制体重。
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来源期刊
Clinical Infectious Diseases
Clinical Infectious Diseases 医学-传染病学
CiteScore
25.00
自引率
2.50%
发文量
900
审稿时长
3 months
期刊介绍: Clinical Infectious Diseases (CID) is dedicated to publishing original research, reviews, guidelines, and perspectives with the potential to reshape clinical practice, providing clinicians with valuable insights for patient care. CID comprehensively addresses the clinical presentation, diagnosis, treatment, and prevention of a wide spectrum of infectious diseases. The journal places a high priority on the assessment of current and innovative treatments, microbiology, immunology, and policies, ensuring relevance to patient care in its commitment to advancing the field of infectious diseases.
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