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比克替拉韦/恩曲他滨/丙酚替诺福韦(B/F/TAF)在包括存在 HIV 耐药和依从性不佳的美国黑人成年人中的高效性。

High efficacy of bictegravir/emtricitabine/tenofovir alafenamide (B/F/TAF) in Black adults in the United States, including those with pre-existing HIV resistance and suboptimal adherence.

机构信息

Gilead Sciences, Inc., Foster City, California, USA.

Chatham CARE Center, Savannah, Georgia, USA.

出版信息

J Med Virol. 2024 Oct;96(10):e29899. doi: 10.1002/jmv.29899.

Abstract

BRAAVE (NCT03631732), a Phase 3b, multicenter, open-label US study, demonstrated the efficacy of switching to bictegravir/emtricitabine/tenofovir alafenamide (B/F/TAF) among Black individuals with suppressed HIV through 48 weeks. Here, 72-week resistance, adherence, and virologic outcomes are presented. Enrollment criteria permitted nonnucleoside reverse transcriptase inhibitor (NNRTI)-resistance (R), protease inhibitor (PI)-R, and certain nucleos(t)ide reverse transcriptase inhibitor (NRTI)-R (M184V/I allowed; ≥3 thymidine analog mutations [TAMs] excluded); but excluded primary integrase strand transfer inhibitor (INSTI)-R. Pre-existing resistance was determined using historical genotypes and retrospective baseline proviral DNA genotyping. Adherence, virologic outcomes, and viral blips were assessed. Of 489 participants receiving B/F/TAF with ≥1 post-switch HIV-1 RNA measurement: pre-existing NRTI-R (15% of participants), M184V/I (11%), ≥1 TAMs (8%), NNRTI-R (22%), and PI-R (13%) were observed; pre-existing INSTI-R substitutions (2%) were detected post-randomization; mean viral blip frequency was 0.9% across all timepoints (unassociated with virologic failure); 24% of participants had <95% adherence (98% of whom had HIV-1 RNA <50 copies/mL at last visit); none had treatment-emergent study-drug resistance. Overall, 99% of participants, including all with baseline NRTI-R/INSTI-R, had HIV-1 RNA <50 copies/mL at the last visit, demonstrating that B/F/TAF maintained virologic suppression through 72 weeks regardless of pre-existing resistance, viral blips, and suboptimal adherence.

摘要

BRAAVE(NCT03631732)是一项 3b 期、多中心、开放标签的美国研究,在 48 周时证明了在抑制 HIV 的黑人个体中切换至比替拉韦/恩曲他滨/丙酚替诺福韦(B/F/TAF)的疗效。在此,报告了 72 周的耐药性、依从性和病毒学结果。入组标准允许存在非核苷类逆转录酶抑制剂(NNRTI)耐药(R)、蛋白酶抑制剂(PI)耐药(R)和某些核苷(酸)逆转录酶抑制剂(NRTI)耐药(M184V/I 允许;排除≥3 个胸苷类似物突变[TAMs]);但排除主要整合酶链转移抑制剂(INSTI)耐药(R)。使用历史基因型和回溯性基线前病毒 DNA 基因分型来确定预先存在的耐药性。评估了依从性、病毒学结果和病毒学突破。在接受 B/F/TAF 治疗且至少有 1 次治疗后 HIV-1 RNA 检测的 489 名参与者中:观察到预先存在的 NRTI-R(15%的参与者)、M184V/I(11%)、≥1 个 TAMs(8%)、NNRTI-R(22%)和 PI-R(13%);随机分组后检测到预先存在的 INSTI-R 替代物(2%);所有时间点的平均病毒学突破频率为 0.9%(与病毒学失败无关);24%的参与者依从性<95%(其中 98%的人在最后一次就诊时 HIV-1 RNA<50 拷贝/mL);没有人出现治疗后耐药。总体而言,包括所有基线 NRTI-R/INSTI-R 患者在内的 99%的参与者在最后一次就诊时 HIV-1 RNA<50 拷贝/mL,这表明 B/F/TAF 通过 72 周维持了病毒学抑制,无论是否存在预先存在的耐药性、病毒学突破和依从性欠佳。

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