BICSTaR的24个月数据显示,比替格拉韦/恩曲他滨/替诺福韦在韩国HIV感染者中的有效性和安全性

IF 2.9 Q2 INFECTIOUS DISEASES
Infection and Chemotherapy Pub Date : 2025-09-01 Epub Date: 2025-09-09 DOI:10.3947/ic.2025.0061
Yeon-Sook Kim, Jun Yong Choi, Dae Won Park, Shin-Woo Kim, Tae Hyong Kim, Julie Ryu, Rebecca Harrison, Jeong-A Lee, Flora Park, Sun Hee Lee
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引用次数: 0

摘要

BICtegravir单片方案是一项多国观察队列研究,评估了BICtegravir /恩曲他滨/替诺福韦阿拉那胺(BIC/FTC/TAF)治疗人类免疫缺陷病毒感染者的有效性和安全性。我们提供了来自韩国参与者的24个月的数据。共纳入88例受试者(36例treatment-naïve [TN], 52例有治疗经验[TE])。在24个月时,100%(29/29)的TN和100%(37/37)的TE参与者携带HIV-1 RNA
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effectiveness and Safety of Bictegravir/Emtricitabine/Tenofovir Alafenamide in People with HIV in Korea: 24-Month Data from BICSTaR.

BICtegravir Single Tablet Regimen is a multi-national observational cohort study evaluating the effectiveness and safety of bictegravir/emtricitabine/tenofovir alafenamide (BIC/FTC/TAF) in people with human immunodeficiency virus. We present 24-month data from participants in Korea. Eighty-eight participants (36 treatment-naïve [TN], 52 treatment-experienced [TE]) were included. At 24 months, 100% (29/29) of TN and 100% (37/37) of TE participants had HIV-1 RNA <50 copies/mL (missing=excluded analysis). BIC/FTC/TAF persistence was 100% (33/33) and 96.1% (49/51) in TN and TE participants, respectively. Drug-related adverse events occurred in 2 TN participants. Improvements in some patient-reported outcomes were observed. BIC/FTC/TAF maintained effectiveness, persistence, and tolerability over 24 months.

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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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