Dolutegravir plus lamivudine for the treatment of HIV-1 infection |
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Authors: | Arturo Ciccullo Gianmaria Baldin Alberto Borghetti |
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Affiliation: | 1. Institute of Clinical Infectious Diseases, Catholic University of the Sacred Heart, Rome, Italyhttps://orcid.org/0000-0001-5941-883X;2. Institute of Clinical Infectious Diseases, Catholic University of the Sacred Heart, Rome, Italy;3. Mater Olbia Hospital, Olbia, Italyhttps://orcid.org/0000-0003-4623-9976;4. UOC Malattie Infettive, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Rome, Italy |
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Abstract: | ABSTRACTIntroduction: Recent data on the 2-drug regimen (2DR) with dolutegravir (DTG) plus lamivudine (3TC) have shown high efficacy and tolerability both in treatment-naïve 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 naïve 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-naïve patients, DTG+3TC has shown non-inferiority compared to standard 3-drug regimens but is less effective in severely immunocompromised naïve 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. |
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Keywords: | HIV dolutegravir lamivudine HAART 2-drug regimens |
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