Switching to Dolutegravir/Lamivudine Two-Drug Regimen: Durability and Virologic Outcomes by Age, Sex, and Race in Routine US Clinical Care

G. Pierone, L. Brunet, J. Fusco, C. Henegar, Supriya Sarkar, J. van Wyk, V. Vannappagari, M. Wohlfeiler, G. Fusco
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Abstract

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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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
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。
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