Dolutegravir plus lamivudine for the treatment of HIV-1 infection

被引:8
|
作者
Ciccullo, Arturo [1 ]
Baldin, Gianmaria [1 ,2 ]
Borghetti, Alberto [3 ]
Di Giambenedetto, Simona [1 ,3 ]
机构
[1] Univ Cattolica Sacro Cuore, Inst Clin Infect Dis, Rome, Italy
[2] Mater Olbia Hosp, Olbia, Italy
[3] IRCCS, Fdn Policlin Univ Agostino Gemelli, UOC Malattie Infett, Rome, Italy
关键词
HIV; dolutegravir; lamivudine; HAART; 2-drug regimens; IMMUNODEFICIENCY-VIRUS TYPE-1; CHRONIC HEPATITIS-B; REVERSE-TRANSCRIPTASE INHIBITORS; TENOFOVIR DISOPROXIL FUMARATE; ONCE-DAILY DOLUTEGRAVIR; INTEGRASE-INHIBITOR; OPEN-LABEL; ANTIRETROVIRAL THERAPY; NAIVE ADULTS; ADVERSE EVENTS;
D O I
10.1080/14787210.2020.1729742
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Introduction: Recent data on the 2-drug regimen (2DR) with dolutegravir (DTG) plus lamivudine (3TC) have shown high efficacy and tolerability both in treatment-naive and experienced HIV-positive patients. Current guidelines recommend DTG+3TC as an alternative to triple antiretroviral therapy (ART) in selected patients to reduce long-term toxicity and costs. Areas covered: This review is intended to provide insight about the efficacy, safety, and tolerability of a 2DR with DTG+3TC in naive and treatment-experienced patients. Expert opinion: Data from clinical trials and from real-life show that DTG+3TC is an effective and safe switch option for the treatment of experienced patients. In treatment-naive patients, DTG+3TC has shown non-inferiority compared to standard 3-drug regimens but is less effective in severely immunocompromised naive patients (i.e. with a CD4+ cell count below 200 cell/mm3); furthermore, current guidelines have upgraded this dual regimen to recommended first-line strategy, but indicate that it should not be used without genotypic resistance results. Moreover, this regimen is not feasible for HBV-coinfected individuals and should not be used during pregnancy. Currently, out of 2-drug regimens, DTG+3TC is one of clinicians' preferred option as it requires no pharmacokinetic booster, has a low risk of drug interaction, and does not require food intake.
引用
收藏
页码:279 / 292
页数:14
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