TY - JOUR
T1 - Dolutegravir plus lamivudine for the treatment of HIV-1 infection
AU - Ciccullo, A.
AU - Baldin, G.
AU - Borghetti, A.
AU - Di Giambenedetto, Simona
PY - 2020
Y1 - 2020
N2 - Introduction: 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.
AB - Introduction: 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.
KW - 2-drug regimens
KW - HAART
KW - HIV
KW - dolutegravir
KW - lamivudine
KW - 2-drug regimens
KW - HAART
KW - HIV
KW - dolutegravir
KW - lamivudine
UR - https://publicatt.unicatt.it/handle/10807/147512
UR - https://www.scopus.com/inward/citedby.uri?partnerID=HzOxMe3b&scp=85079731859&origin=inward
UR - https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85079731859&origin=inward
U2 - 10.1080/14787210.2020.1729742
DO - 10.1080/14787210.2020.1729742
M3 - Article
SN - 1478-7210
SP - 1-14-14
JO - Expert Review of Anti-Infective Therapy
JF - Expert Review of Anti-Infective Therapy
IS - na
ER -