Clinic of Infectious Diseases, 'Alma Mater Studiorum' University of Bologna, S. Orsola-Malpighi Hospital, Bologna, Italy.
Unit of Microbiology, 'Alma Mater Studiorum' University of Bologna, S. Orsola-Malpighi Hospital, Bologna, Italy.
J Antimicrob Chemother. 2020 Nov 1;75(11):3327-3333. doi: 10.1093/jac/dkaa319.
Antiretroviral dual regimens including lamivudine and one boosted PI or dolutegravir are warranted in order to optimize combination ART (cART), prevent long-term toxicity and reduce the cost of treatments.
We hypothesized that a maintenance dual regimen of lamivudine plus raltegravir would be effective and as well tolerated as the dual maintenance combination of lamivudine plus dolutegravir.
We performed an observational, retrospective study of HIV-infected patients on suppressive ART who switched to a dual regimen containing lamivudine 300 mg once daily plus raltegravir 1200 mg once daily or dolutegravir 50 mg once daily.
In total, 109 patients (79 men; mean age 46.4 years; mean CD4+ T lymphocyte count 605 cells/mm3) were enrolled. Overall, 50 subjects switched to lamivudine plus raltegravir (Group A) and 59 to lamivudine plus dolutegravir (Group B). After 12 months, 45 patients (90%) in Group A and 52 (88.1%) in Group B had HIV RNA <20 copies/mL. No patients had severe adverse effects in either group, and the percentages of patients with mild adverse effects were comparable, except for a higher incidence of headache and sleeping disturbances in Group B than in Group A (30.5% versus 14%, P < 0.001). A comparable and non-significant weight increase was reported in both groups (+1.91 kg in Group A and +2.28 kg in Group B).
In our study, dual therapies containing lamivudine plus raltegravir or dolutegravir in virologically suppressed patients showed high and comparable efficacy, as well as good tolerability.
为了优化联合抗逆转录病毒治疗(cART)、预防长期毒性和降低治疗成本,需要使用包含拉米夫定和一种增效 PI 或多替拉韦的抗逆转录病毒双联方案。
我们假设拉米夫定联合雷迪帕韦维持治疗方案与拉米夫定联合多替拉韦维持治疗方案同样有效且耐受性良好。
我们对接受抑制性抗逆转录病毒治疗的 HIV 感染者进行了一项观察性、回顾性研究,这些患者转换为包含每日一次 300mg 拉米夫定和每日一次 1200mg 雷迪帕韦或每日一次 50mg 多替拉韦的双联方案。
共纳入 109 例患者(79 例男性;平均年龄 46.4 岁;平均 CD4+T 淋巴细胞计数 605 个/立方毫米)。共有 50 例患者转换为拉米夫定联合雷迪帕韦(A 组),59 例转换为拉米夫定联合多替拉韦(B 组)。12 个月后,A 组 45 例(90%)和 B 组 52 例(88.1%)患者的 HIV RNA<20 拷贝/毫升。两组均无严重不良事件,且轻度不良事件的患者比例相当,除 B 组头痛和睡眠障碍的发生率高于 A 组(30.5%比 14%,P<0.001)外。两组患者的体重均有相似且无统计学意义的增加(A 组增加 1.91kg,B 组增加 2.28kg)。
在我们的研究中,在病毒学抑制的患者中,包含拉米夫定加雷迪帕韦或多替拉韦的双联疗法具有较高的疗效和良好的耐受性。