转用多罗替韦/拉米夫定双药方案:美国常规临床护理中按年龄、性别和种族分列的耐久性和病毒学结果

G. Pierone, L. Brunet, J. Fusco, C. Henegar, Supriya Sarkar, J. van Wyk, V. Vannappagari, M. Wohlfeiler, G. Fusco
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引用次数: 0

摘要

目的 双药方案(2DR)可解决药物间相互作用和毒性问题。多罗替拉韦/拉米夫定(DTG/3TC)2DR在美国获批用于病毒载量小于50拷贝/毫升的无治疗经验者和有治疗经验者。本研究描述了按年龄、性别和种族分层的有治疗经验者的实际 DTG/3TC 2DR 治疗结果。方法 从 OPERA® 队列中纳入了病毒载量<50拷贝/毫升、在 2019 年 4 月 8 日至 2021 年 4 月 30 日期间根据标签从常用三药方案转为 DTG/3TC 2DR 的 HIV 感染者。估算了病毒学控制丧失(首次病毒载量≥50拷贝/毫升)、确诊病毒学失败(2次病毒载量≥200拷贝/毫升或1次病毒载量≥200拷贝/毫升后停药)和DTG/3TC 2DR停药的总体发生率(泊松回归),并按年龄、性别和种族进行了分层。结果 对纳入的 787 人进行了中位数为 13.6 个月(IQR:8.2,22.3)的随访。确认病毒学失败的人数少于 5 人。病毒学控制丧失率为每 100 人年 14.0 例(95% CI:11.7, 16.8)。DTG/3TC 2DR 的停药率为每 100 人年 17.5 例(95% CI:15.0,20.3);4% 的停药原因与治疗有关(病毒血症、不良诊断、副作用、实验室异常)。在所有结果中,不同年龄、性别和种族的发病率具有可比性。结论 这项描述性研究表明,对于切换时病毒载量小于 50 拷贝/毫升的 HIV 感染者,无论其年龄、性别或种族如何,DTG/3TC 2DR 都是一种有效且耐受性良好的治疗方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Switching to Dolutegravir/Lamivudine Two-Drug Regimen: Durability and Virologic Outcomes by Age, Sex, and Race in Routine US Clinical Care
Purpose Two-drug regimens (2DR) may address drug–drug interactions and toxicity concerns. Dolutegravir/lamivudine (DTG/3TC) 2DR was approved in the US for both treatment-naïve and treatment-experienced individuals with a viral load <50 copies/mL. This study describes real-world DTG/3TC 2DR treatment outcomes among treatment-experienced individuals, stratified by age, sex, and race. Methods From the OPERA® cohort, people with HIV with a viral load <50 copies/mL who switched from a commonly used three-drug regimen to DTG/3TC 2DR as per the label between April 8, 2019 and April 30, 2021 were included. Incidence rates (Poisson regression) for loss of virologic control (first viral load ≥50 copies/mL), confirmed virologic failure (2 viral loads ≥200 copies/mL or discontinuation after 1 viral load ≥200 copies/mL), and DTG/3TC 2DR discontinuation were estimated overall and stratified by age, sex, and race. Results The 787 individuals included were followed for a median of 13.6 months (IQR: 8.2, 22.3). Confirmed virologic failure occurred in ≤5 individuals. Loss of virologic control occurred at a rate of 14.0 per 100 person-years (95% CI: 11.7, 16.8). DTG/3TC 2DR discontinuation occurred at a rate of 17.5 per 100 person-years (95% CI: 15.0, 20.3); 4% discontinued for treatment-related reasons (viremia, adverse diagnosis, side effect, lab abnormality). For all outcomes, incidence rates were comparable across strata of age, sex, and race. Conclusion This descriptive study demonstrates that DTG/3TC 2DR is an effective and well-tolerated treatment option for people with HIV with a viral load <50 copies/mL at switch, regardless of their age, sex, or race.
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