Rapid start with bictegravir/emtricitabine/tenofovir alafenamide (B/F/TAF) as initial treatment in people with human immunodeficiency virus-1 (HIV-1): A systematic literature review of clinical and patient-reported outcomes.

IF 2.8 3区 医学 Q2 INFECTIOUS DISEASES
HIV Medicine Pub Date : 2025-06-26 DOI:10.1111/hiv.70065
Jade Ghosn, Jeremy Chow, Monica Gandhi, Miguel Górgolas, Aws Al-Hayani, Hansel Tookes, Max Lee, Emily F Kaiser, David Malebranche, Fernando Alvarez Bognar, Bhumi Gandhi-Patel, Lili Dai
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引用次数: 0

Abstract

Background: Treatment guidelines recommend rapid antiretroviral therapy (ART) initiation among eligible people with HIV to improve treatment outcomes and reduce HIV transmission. Bictegravir/emtricitabine/tenofovir alafenamide (B/F/TAF), an integrase strand transfer inhibitor-based single-tablet regimen, is recommended for rapid start in US and European guidelines. This systematic literature review synthesized evidence on the efficacy, safety and effect on patient-reported outcomes (PROs) of B/F/TAF rapid start among newly diagnosed people with HIV.

Methods: MEDLINE, Embase, Cochrane Database of Systematic Reviews and Cochrane Central Register of Controlled Trials databases were searched in January 2024, supplemented by searches of conference proceedings and clinical trial records. English-language interventional studies of B/F/TAF rapid start among ART-naïve people with HIV reporting efficacy, safety or PROs were eligible. Study quality was assessed using York Centre for Reviews and Dissemination or Risk Of Bias In Non-randomized Studies of Interventions checklists. Results were synthesized narratively.

Results: Across eight included studies, 745 people with HIV received B/F/TAF rapid start, 171 received rapid start comparators and 255 received non-rapid start comparators. At Weeks 24 and 48, 80%-94% and 74%-96% of people with HIV treated with B/F/TAF rapid start achieved viral load <50 copies/mL, respectively. Treatment discontinuation due to adverse events was 0%-3%, and grade 3/4 adverse events occurred in 0%-3% of people with HIV receiving B/F/TAF rapid start. Rapid start improved engagement in care over traditional non-rapid start approaches, and B/F/TAF rapid start reduced anxiety and improved quality of life among people with HIV. Limitations of the review included heterogeneous study definitions of "rapid start" and limited data availability.

Conclusions: B/F/TAF rapid start was efficacious, safe and associated with high engagement in care and improved PROs.

快速启动比替格拉韦/恩曲他滨/替诺福韦alafenamide (B/F/TAF)作为人类免疫缺陷病毒-1 (HIV-1)患者的初始治疗:临床和患者报告结果的系统文献综述。
背景:治疗指南建议在符合条件的艾滋病毒感染者中开始快速抗逆转录病毒治疗(ART),以改善治疗效果并减少艾滋病毒传播。Bictegravir/emtricitabine/替诺福韦alafenamide (B/F/TAF)是一种基于整合酶链转移抑制剂的单片方案,在美国和欧洲的指南中被推荐用于快速启动。本系统文献综述综合了新诊断HIV感染者B/F/TAF快速启动的有效性、安全性和对患者报告结局(pro)的影响的证据。方法:检索2024年1月的MEDLINE、Embase、Cochrane系统评价数据库和Cochrane中央对照试验注册数据库,并辅以会议记录和临床试验记录。在ART-naïve报告疗效、安全性或PROs的HIV患者中进行B/F/TAF快速启动的英语介入研究符合条件。研究质量采用约克中心评价和传播或非随机干预研究的偏倚风险清单进行评估。对结果进行叙述性综合。结果:在8项纳入的研究中,745名HIV感染者接受了B/F/TAF快速启动,171人接受了快速启动比较,255人接受了非快速启动比较。在第24周和第48周,接受B/F/TAF快速启动治疗的HIV患者中,80%-94%和74%-96%的人达到了病毒载量。结论:B/F/TAF快速启动有效、安全,并且与高参与度的护理和改善的PROs相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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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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