De Socio Giuseppe Vittorio, Tordi Sara, Altobelli Debora, Gidari Anna, Zoffoli Anastasia, Francisci Daniela
Department of Medicine, Clinic of Infectious Diseases, "Santa Maria della Misericordia" Hospital, University of Perugia, 06129 Perugia, Italy.
J Clin Med. 2023 Dec 18;12(24):7759. doi: 10.3390/jcm12247759.
The aim of the study is to evaluate the effectiveness, safety, and tolerability of a two-drug regimen (2-DR) dolutegravir/lamivudine (DTG/3TC) versus a three-drug regimen (3-DR) tenofovir alafenamide/emtricitabine/bictegravir (TAF/FTC/BIC) in a real-life cohort of HIV-1 virologically suppressed treatment-experienced (TE) people living with HIV (PLWH).
This was a single-center, retrospective, observational study analyzing adult TE PLWH who started the 2-DR or 3-DR between January 2018 and January 2023. All PLWH with a viral load (VL) <50 copies/mL at the time of switching, and a follow-up of more than 6 months or interruption of treatment at any time, were included.
A total of 324 PLWH were included; of these, 110 (34%) were on the 2-DR and 214 (66%) were on the 3-DR. Most patients remained on therapy in both groups (93.6% 2-DR versus 90.2% 3-DR) and, at the last control, 99.1% achieved VL < 50 copies/mL with the 2-DR versus 97.2% with the 3-DR ( = 0.260). No virological failures occurred in either group. Adverse events occurred in a few cases: four (3.6%) in the 2-DR group and five (2.3%) in the 3-DR group ( = 0.500). The median follow-up-time was 19.6 months for the 2-DR and 27.5 months for the 3-DR.
Our study shows a similar effectiveness and safety profile in virologically suppressed PLWH switching to DTG/3TC or TAF/FTC/BIC.
本研究旨在评估在接受过治疗且病毒得到抑制的HIV-1感染者(PLWH)的真实队列中,双药方案(2-DR)多替拉韦/拉米夫定(DTG/3TC)与三药方案(3-DR)替诺福韦艾拉酚胺/恩曲他滨/比克替拉韦(TAF/FTC/BIC)的有效性、安全性和耐受性。
这是一项单中心、回顾性观察研究,分析了2018年1月至2023年1月期间开始使用2-DR或3-DR的成年接受过治疗的PLWH。纳入所有在换药时病毒载量(VL)<50拷贝/mL,且随访超过6个月或在任何时间中断治疗的PLWH。
共纳入324例PLWH;其中,110例(34%)接受2-DR治疗,214例(66%)接受3-DR治疗。两组中大多数患者继续接受治疗(2-DR组为93.6%,3-DR组为90.2%),在最后一次对照时,2-DR组99.1%的患者实现VL<50拷贝/mL,3-DR组为97.2%(P = 0.260)。两组均未发生病毒学失败。少数病例出现不良事件:2-DR组4例(3.6%),3-DR组5例(2.3%)(P = 0.500)。2-DR组的中位随访时间为19.6个月,3-DR组为27.5个月。
我们的研究表明,在病毒得到抑制的PLWH中,换用DTG/3TC或TAF/FTC/BIC的有效性和安全性相似。