Department of Internal Medicine, National Taiwan University Hospital and National Taiwan University College of Medicine, Taipei, Taiwan; Min-Sheng General Hospital, Taoyuan, Taiwan.
Department of Internal Medicine, National Taiwan University Hospital and National Taiwan University College of Medicine, Taipei, Taiwan.
J Microbiol Immunol Infect. 2023 Oct;56(5):988-995. doi: 10.1016/j.jmii.2023.07.013. Epub 2023 Aug 4.
Antiretroviral regimens containing a second-generation integrase strand-transfer inhibitor (INSTI) plus 2 nucleos(t)ide reverse-transcriptase inhibitors (NRTIs) are the recommended therapy for people with HIV (PWH) who are antiretroviral-naïve or on stable antiretroviral therapy (ART) with viral suppression. Real-world data on the virologic effectiveness of co-formulated bictegravir/emtricitabine/tenofovir alafenamide (BIC/FTC/TAF) among PWH with virologic failure while receiving other ART remain sparse.
We retrospectively reviewed the medical records of PWH who had viral rebound with plasma HIV RNA >1000 copies/mL and were switched to either dolutegravir combined with 2 NRTIs or BIC/FTC/TAF. The primary end point was re-achieving viral suppression within the first 48 weeks of switch. The association between NRTI-related resistance-associated mutations (RAMs) and virologic effectiveness was examined.
Seventy-nine PWH with viral rebound while receiving other antiretroviral regimens were included. Within the first 48 weeks of switch, the overall probability of re-achieving viral suppression was 79.7% (82.5% [33/40] and 76.9% [30/39] for BIC/FTC/TAF and dolutegravir-based regimens, respectively, p = 0.78). PWH with a higher CD4 lymphocyte count (adjusted odds ratio, per 100-cell/mm increase, 1.41; 95% confidence interval, 1.02-1.95) were more likely to re-achieve viral suppression. Among PWH switching to BIC/FTC/TAF who had pre-existing RAMs to NRTIs before switch, 14 of 15 (93.3%) successfully achieved viral suppression.
Switching to BIC/FTC/TAF and dolutegravir-based regimens could re-achieve viral suppression in four-fifth of the PWH who experienced viral rebound during treatment with other antiretroviral regimens. Pre-existing NRTI-related RAMs did not have adverse impact on the effectiveness of dolutegravir combined with 2 NRTIs or BIC/FTC/TAF.
含有第二代整合酶链转移抑制剂(INSTI)加 2 种核苷(酸)逆转录酶抑制剂(NRTIs)的抗逆转录病毒方案是用于初治或正在接受稳定抗逆转录病毒治疗(ART)且病毒得到抑制的 HIV 感染者(PWH)的推荐疗法。在接受其他 ART 治疗时出现病毒学失败的 PWH 中,二合一贝达喹啉/恩曲他滨/替诺福韦艾拉酚胺(BIC/FTC/TAF)的联合方案在病毒学疗效方面的真实世界数据仍然很少。
我们回顾性地审查了那些血浆 HIV RNA 反弹>1000 拷贝/ml 且转为多替拉韦联合 2 种 NRTIs 或 BIC/FTC/TAF 的 PWH 的医疗记录。主要终点是在转换后的头 48 周内重新达到病毒抑制。研究了 NRTI 相关耐药相关突变(RAM)与病毒学疗效之间的关系。
纳入了 79 例在接受其他抗逆转录病毒方案治疗时发生病毒反弹的 PWH。在转换后的头 48 周内,总体上重新达到病毒抑制的概率为 79.7%(BIC/FTC/TAF 和多替拉韦方案分别为 82.5%[33/40]和 76.9%[30/39],p=0.78)。CD4 淋巴细胞计数较高的 PWH(每增加 100 个细胞/mm 的调整优势比,1.41;95%置信区间,1.02-1.95)更有可能重新达到病毒抑制。在转换为 BIC/FTC/TAF 的 PWH 中,有 15 例在转换前存在 NRTI 相关 RAM,其中 14 例(93.3%)成功达到病毒抑制。
在因其他抗逆转录病毒方案治疗而发生病毒学反弹的 PWH 中,有五分之四可通过转换为 BIC/FTC/TAF 和多替拉韦方案重新达到病毒抑制。在转换为多替拉韦联合 2 种 NRTIs 或 BIC/FTC/TAF 时,预先存在的 NRTI 相关 RAM 对疗效没有不良影响。