Effectiveness of dolutegravir-based regimens compared to raltegravir-, elvitegravir-, bictegravir, and darunavir-based regimens among older adults with HIV in the Veterans Aging Cohort Study (VACS).

IF 2.1 4区 医学 Q3 INFECTIOUS DISEASES AIDS Research and Therapy Pub Date : 2024-12-21 DOI:10.1186/s12981-024-00681-w
Lei Yan, Cassidy E Henegar, Vincent C Marconi, Kirsha S Gordon, Charles Hicks, Vani Vannappagari, Amy C Justice, Mihaela Aslan
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Abstract

Background: Real-world data on treatment patterns and clinical outcomes for newer drugs, including integrase strand transfer inhibitors, among older people with human immunodeficiency virus (PWH) are limited.

Methods: This cohort study included PWH enrolled in the Veterans Aging Cohort Study (VACS) who were prescribed a standard 3-drug antiretroviral therapy (ART) regimen containing dolutegravir (DTG), bictegravir (BIC), cobicistat boosted elvitegravir (EVG), raltegravir (RAL), or darunavir/ritonavir (DRV) plus 2 nucleoside reverse transcriptase inhibitors between January 1, 2014, and March 31, 2020, and who were ≥50 years at regimen initiation. The association between regimen and virologic effectiveness or discontinuation was assessed using logistic regression models with inverse probability of treatment weights. Pairwise comparisons were made between DTG-based regimen and each of the other 3-drug regimens, stratified by ART experience.

Results: Among 15,702 PWH (across treatment groups, median age 58-62 years; 94-98% male; 5-11% Hispanic; 44-60% Black; 29-42% White), 5,800 received DTG-based regimens, 2,081 BIC-based regimens, 4,159 EVG-based regimens, 1,607 RAL-based regimens, and 2,055 received DRV-based regimens. Among ART-naïve PWH, there were no statistical differences in the odds of virologic suppression, and 6- and 12-month discontinuations were higher in those on DRV. Among ART-experienced PWH, compared to DTG, those on RAL and DRV were less likely to be suppressed at 6 months (RAL vs DTG: aOR 0.64, 95% CI 0.51-0.81; DRV vs DTG: aOR 0.63, 95% CI 0.51-0.76) and those on EVG and DRV were less likely suppressed at 12 months (EVG vs DTG: aOR 0.82, 95% CI 0.68-0.99; DRV vs DTG: aOR 0.64, 95% CI 0.52-0.80). Those on DRV were more likely to have virologic failure within 12 months (aOR 1.96, 95% CI 1.30-2.97). Six- and 12-month discontinuations were higher in those on RAL and DRV, but less likely for BIC-based regimens.

Conclusions: DTG-based regimens demonstrated higher levels of effectiveness and durability compared to DRV- or RAL-based regimens and had similar treatment responses as BIC- and EVG-based regimens among ART-experienced older PWH.

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在退伍军人老龄化队列研究(VACS)中,与以雷替重力韦、依替重力韦、比替重力韦和达拉那韦为基础的方案相比,以多替重力韦为基础的方案在艾滋病毒老年人中的有效性
背景:包括整合酶链转移抑制剂在内的新药在老年人类免疫缺陷病毒(PWH)患者中的治疗模式和临床结果的实际数据有限。方法:该队列研究纳入了参加退伍军人老龄化队列研究(VACS)的PWH,他们在2014年1月1日至2020年3月31日期间接受了标准的3药抗逆转录病毒治疗(ART)方案,其中包括dolutegravir (DTG)、bictegravir (BIC)、cobicistat增强elvitegravir (EVG)、raltegravir (RAL)或darunavir/ritonavir (DRV)加2种核苷类逆转录酶抑制剂,并且在方案开始时年龄≥50岁。使用具有治疗权重逆概率的逻辑回归模型评估方案与病毒学有效性或停药之间的关系。将基于dtg的方案与其他3种药物方案进行两两比较,并按ART经验分层。结果:15702名PWH患者(各治疗组,中位年龄58 ~ 62岁;94 - 98%的男性;5 - 11%的拉美裔;44 - 60%黑色;5800人接受了基于dtg的方案,2081人接受了基于bic的方案,4159人接受了基于evg的方案,1607人接受了基于ral的方案,2055人接受了基于drv的方案。在ART-naïve PWH组中,病毒学抑制的几率没有统计学差异,DRV组6个月和12个月的停药率更高。在接受art治疗的PWH中,与DTG相比,接受RAL和DRV治疗的PWH在6个月时受到抑制的可能性更小(RAL vs DTG: aOR 0.64, 95% CI 0.51-0.81;DRV vs DTG: aOR 0.63, 95% CI 0.51-0.76), EVG和DRV在12个月时抑制的可能性较小(EVG vs DTG: aOR 0.82, 95% CI 0.68-0.99;DRV vs DTG: aOR 0.64, 95% CI 0.52-0.80)。接受DRV治疗的患者更有可能在12个月内出现病毒学失败(aOR 1.96, 95% CI 1.30-2.97)。服用RAL和DRV的患者停药6个月和12个月的比例较高,但服用bic的患者停药的可能性较低。结论:与基于DRV或ral的方案相比,基于dtg的方案显示出更高的有效性和持久性,并且在经历过art的老年PWH中具有与基于BIC和evg的方案相似的治疗反应。
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来源期刊
AIDS Research and Therapy
AIDS Research and Therapy INFECTIOUS DISEASES-
CiteScore
3.80
自引率
4.50%
发文量
51
审稿时长
16 weeks
期刊介绍: AIDS Research and Therapy publishes articles on basic science, translational, clinical, social, epidemiological, behavioral and educational sciences articles focused on the treatment and prevention of HIV/AIDS, and the search for the cure. The Journal publishes articles on novel and developing treatment strategies for AIDS as well as on the outcomes of established treatment strategies. Original research articles on animal models that form an essential part of the AIDS treatment research are also considered
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