Calza Leonardo, Colangeli Vincenzo, Giglia Maddalena, Rigamonti Claudio, Bon Isabella, Cretella Silvia, Viale Pierluigi
Department of Medical and Surgical Sciences, Unit of Infectious Diseases, S.Orsola Hospital, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy; and.
Department of Medical and Surgical Sciences, Unit of Microbiology, S.Orsola Hospital, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.
J Acquir Immune Defic Syndr. 2025 May 1;99(1):93-97. doi: 10.1097/QAI.0000000000003600.
Dual regimen dolutegravir/lamivudine (DOL/3TC) showed potent efficacy and favorable safety in both antiretroviral therapy-naive and therapy-experienced patients, but data from real life about naive people with high-level viremia are still lacking.
We performed a retrospective cohort study of people living with HIV who were naive to antiretroviral therapy, had baseline HIV-1 RNA ranging from 100,000 to 500,000 copies/mL, and initiated DOL/3TC. Virologic efficacy and changes in immunologic parameters after 12 months of treatment were evaluated and compared with highly viremic people living with HIV who started a triple antiretroviral combination.
Inclusion criteria were met by 58 patients with median age of 43.4 years. At baseline, mean HIV RNA was 5.4 log 10 and mean CD4 T lymphocyte count was 488 cells/mm 3 . HIV RNA <50 copies/mL was obtained in 45 patients (77.6% in the intention-to-treat analysis) after 6 months and in 53 patients (91.4%) after 12 months. Reasons for treatment failure were virologic failure in 2 cases and adverse events in 3 cases. No significant changes in median value of lipids were reported, while there was a not significant increase in body weight (+1.18 kg). Virologic and immunologic response at month 12 in patients on DOL/3TC was comparable with that observed in 50 naive patients with high-level viremia and starting a triple antiretroviral therapy.
In this real-life cohort of naive patients with high-level viremia, DOL/3TC was associated with high virologic efficacy and good tolerability after 12 months, supporting use of this dual regimen also in persons with high initial viremia.
多替拉韦/拉米夫定双药方案(DOL/3TC)在初治和经治抗逆转录病毒治疗患者中均显示出强效疗效和良好安全性,但关于初治且病毒血症水平高的患者的真实生活数据仍很缺乏。
我们对未接受过抗逆转录病毒治疗、基线HIV-1 RNA水平在100,000至500,000拷贝/毫升之间并开始使用DOL/3TC的HIV感染者进行了一项回顾性队列研究。评估了治疗12个月后的病毒学疗效和免疫参数变化,并与开始使用三联抗逆转录病毒联合治疗的高病毒血症HIV感染者进行了比较。
58例患者符合纳入标准,中位年龄为43.4岁。基线时,平均HIV RNA为5.4 log10,平均CD4 T淋巴细胞计数为488个细胞/立方毫米。6个月后,45例患者(意向性分析中占77.6%)的HIV RNA<50拷贝/毫升,12个月后53例患者(91.4%)达到该水平。治疗失败的原因包括2例病毒学失败和3例不良事件。脂质中位数无显著变化,而体重有不显著增加(+1.18千克)。接受DOL/3TC治疗的患者在第12个月时的病毒学和免疫反应与50例初治且高病毒血症并开始三联抗逆转录病毒治疗的患者所观察到的反应相当。
在这个初治且高病毒血症的真实生活队列中,DOL/3TC在12个月后具有高病毒学疗效和良好耐受性,支持在初始病毒血症高的患者中也使用这种双药方案。