Efficacy and Tollerability of INI-Based 2-Drug Regimen in Virosuppressed Persons Living with HIV: A Systematic Review and Meta-Analysis.

IF 2.8 Q2 INFECTIOUS DISEASES
Antonio Russo, Salvatore Martini, Mariantonietta Pisaturo, Maria Grazia Palamone, Maria Teresa Russo, Verdiana Zollo, Roberta Palladino, Pierantonio Grimaldi, Alberto Borghetti, Giuseppe Vittorio De Socio, Massimiliano Fabbiani, Nicola Coppola
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Abstract

Background: The aim of this meta-analysis was to synthesize the available evidence from the literature on the efficacy and safety of integrase inhibitor-based two drug regimens compared to triple drug regimens in virosuppressed people living with HIV (PLWH) in a long-term follow-up (at 96 weeks).

Materials and methods: A systematic review and meta-analysis were conducted to evaluate the efficacy, safety, and adverse drug reactions leading to discontinuation of two drug regimens compared to triple drug regimens in virosuppressed PLWH patients at 96 weeks of follow-up. We searched MEDLINE, Google Scholar, and the Cochrane Library up to March 15, 2024, and studies were selected for eligibility based on predefined criteria. Data were extracted independently by two reviewers, and risk ratios (RRs) were calculated as the measure of association between therapy and incidence of events.

Results: Six studies were included in the analysis, both clinical trials and observational studies. The two drug regimens included cabotegravir/rilpivirine, dolutegravir/lamivudine, and dolutegravir/rilpivirine. No significant differences were observed in treatment failure (RR, 0.77; 95% confidence interval [CI], 0.53-1.13; P=0.182), virological failure (RR, 0.79; 95% CI, 0.48-1.29; P=0.341), adverse drug reactions leading to discontinuation (RR, 1.74; 95% CI, 0.73-4.17; P=0.215), or appearance of mutation (RR, 2.48; 95% CI, 0.33-18.68; P=0.379) between two drug regimen and triple drug regimen groups at 96 weeks of follow up.

Conclusion: The meta-analysis provide an overview of the available evidence and supports the use of two drug regimens as an option for simplifying treatment and improving clinical outcomes in virosuppressed PLWH.

基于 INI 的 2 种药物疗法对病毒抑制型 HIV 感染者的疗效和耐受性:系统回顾与元分析》。
背景:本荟萃分析旨在综合现有文献中关于整合酶抑制剂为基础的两种药物治疗方案与三种药物治疗方案在长期随访(96周)中对受病毒抑制的艾滋病病毒感染者(PLWH)的疗效和安全性的证据:我们进行了一项系统综述和荟萃分析,以评估病毒抑制型艾滋病病毒感染者在随访 96 周时,与三联药物治疗方案相比,两联药物治疗方案的疗效、安全性和导致停药的药物不良反应。我们检索了截至 2024 年 3 月 15 日的 MEDLINE、Google Scholar 和 Cochrane 图书馆,并根据预先确定的标准筛选出符合条件的研究。数据由两名审稿人独立提取,并计算风险比(RRs)作为衡量治疗与事件发生率之间关联的指标:共有六项研究被纳入分析,其中既有临床试验,也有观察性研究。两种药物治疗方案包括卡博替拉韦/利匹韦林、多罗替拉韦/拉米夫定和多罗替拉韦/利匹韦林。在治疗失败(RR,0.77;95% 置信区间[CI],0.53-1.13;P=0.182)、病毒学失败(RR,0.79;95% CI,0.48-1.29;P=0.341)、导致停药的药物不良反应(RR,1.74;95% CI,0.73-4.17;P=0.215),或出现突变(RR,2.48;95% CI,0.33-18.68;P=0.379):荟萃分析概述了现有的证据,并支持使用两种药物治疗方案作为简化病毒抑制型 PLWH 治疗和改善临床疗效的一种选择。
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
Infection and Chemotherapy
Infection and Chemotherapy INFECTIOUS DISEASES-
CiteScore
6.60
自引率
11.90%
发文量
71
审稿时长
22 weeks
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