Eron Joseph J, Ramgopal Moti, Osiyemi Olayemi, Mckellar Mehri, Slim Jihad, DeJesus Edwin, Arora Priyanka, Blair Christiana, Hindman Jason T, Wilkin Aimee
The University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
Midway Research Center, Fort Pierce, Florida, USA.
HIV Med. 2025 Feb;26(2):302-307. doi: 10.1111/hiv.13721. Epub 2024 Oct 6.
Treatment for people with HIV-1 and end-stage kidney disease (ESKD) on haemodialysis (HD) has previously required complex dose-adjusted regimens, with limited data on the use of a single-tablet regimen in this population. Our aim was to assess the efficacy and safety of once-daily bictegravir/emtricitabine/tenofovir alafenamide (B/F/TAF) and to evaluate the pharmacokinetics of bictegravir (BIC) in adults with HIV-1 and ESKD on HD.
We performed an open-label extension (OLE) of an open-label, multicentre, single-group phase 3b study (NCT02600819) of adults with ESKD on HD and HIV-1 with virological suppression. Participants switched to elvitegravir/cobicistat/F/TAF (E/C/F/TAF) 150/150/200/10 mg for 96 weeks, following which a subgroup of US participants entered an OLE phase in which they switched to B/F/TAF 50/200/25 mg for 48 weeks, returning for study visits at weeks 4 and 12, and every 12 weeks thereafter. Study assessments included virological response, safety and pharmacokinetic analysis of BIC.
Ten participants entered the OLE (median age, 55 years). Virological suppression (HIV-1 RNA <50 copies/mL) was maintained in all participants over 48 weeks of B/F/TAF treatment. B/F/TAF was well tolerated, with no treatment discontinuations. Mean BIC trough concentrations were lower than those previously reported for people with HIV-1 with normal kidney function, but remained four- to seven-fold higher than the established protein-adjusted 95% effective concentration against wild-type HIV-1.
These findings support the use of the once-daily B/F/TAF single-tablet regimen for people with HIV-1 and ESKD on HD. This regimen offers a convenient treatment option for this population as it reduces the need for dose adjustment, eases pill burden and avoids potential drug-drug interactions associated with alternatives that may impact individuals on multiple medications or awaiting transplantation.
先前,接受血液透析(HD)的HIV-1感染和终末期肾病(ESKD)患者的治疗需要复杂的剂量调整方案,关于该人群使用单片复方制剂的数据有限。我们的目的是评估每日一次的比克替拉韦/恩曲他滨/替诺福韦艾拉酚胺(B/F/TAF)的疗效和安全性,并评估比克替拉韦(BIC)在接受HD治疗的HIV-1感染和ESKD成人患者中的药代动力学。
我们对一项开放标签、多中心、单组3b期研究(NCT02600819)进行了开放标签扩展(OLE),该研究针对接受HD治疗且病毒学得到抑制的HIV-1感染和ESKD成人患者。参与者先服用埃替拉韦/考比司他/F/TAF(E/C/F/TAF)150/150/200/10毫克,为期96周,之后,美国的一部分参与者进入OLE阶段,在此阶段他们改用B/F/TAF 50/200/25毫克,为期48周,并在第4周和第12周以及此后每12周返回进行研究访视。研究评估包括病毒学反应、安全性以及BIC的药代动力学分析。
10名参与者进入了OLE阶段(中位年龄55岁)。在接受B/F/TAF治疗的48周内,所有参与者均维持了病毒学抑制(HIV-1 RNA<50拷贝/毫升)。B/F/TAF耐受性良好,无人因治疗中断。BIC的平均谷浓度低于先前报道的肾功能正常的HIV-1感染者,但仍比针对野生型HIV-1确定的蛋白校正95%有效浓度高4至7倍。
这些发现支持在接受HD治疗的HIV-1感染和ESKD患者中使用每日一次的B/F/TAF单片复方制剂。该方案为这一人群提供了一种方便的治疗选择,因为它减少了剂量调整的需求,减轻了服药负担,并避免了与可能影响正在服用多种药物或等待移植的个体的替代方案相关的潜在药物相互作用。