P-353. Ten Years Results on the Effectiveness and Safety of DTG+3TC as a Switch Regimen in a Multicenter Cohort
Year: 2026
Type: article
Study design: Observational Study
Abstract: Background We aim to assess the efficacy, safety and tolerability of DTG+3TC as a switch regimen after 10 years of its introduction in clinical practice. Methods An observational study was conducted with virologically suppressed PLWH switching to DTG+3TC in a multicenter cohort. Exclusion criteria included HBsAg+ status and M184V resistance mutation. We employed Kaplan-Meyer survival analysis for virological failure (VF) and treatment discontinuation (TD), Cox-regression for VF or TD predictors, and linear mixed models for immunological and metabolic parameter changes. Results We enrolled 2430 PLWH: 1587 (65.3%) were males, with a median age of 54.5 yrs. Full population characteristics are shown in Table1. During 9199 PYFU, we observed 82 VF (0.9 per 100 PYFU); no emergent resistance mutations were registered among VF. Estimated probabilities of maintaining virological suppression (VS) at 240 and 480 wks were 96.2% and 92.8%, respectively. At a multivariate analysis, a history of at least one previous VF before switch (vs no event, aHR 2.09, p=0.005) and a time of VS < 8 years before switch (vs VS > 8 years, aHR 1.82, p=0.021) were significantly associated with a higher risk of VF. During 9287 PYFU, we observed 339 TD (3.7 per 100 PYFU). Estimated probabilities of maintaining DTG/3TC were 83.8% at 240 wks and 79.4% at 480 wks. Discontinuations for toxicity were 78 (23.0% of all TD), with CNS toxicity accounting for 25 cases. Other frequent reasons for TD were: switch to CAB+RPV (64, 18.9%) and treatment intensification (32, 9.4%). At a multivariate analysis, we found that a HIV-RNA peak > 500.000 cps/mL (aHR 1.55, p=0.006) and the presence of HBcAb (aHR 1.60, p=0.002) were significantly associated with a higher risk of TD; meanwhile, the presence of DTG in the ARV regimen before switch, (aHR 0.51, p=0.001) was inversely correlated with TD risk. After 240 weeks, we registered a significant improvement in both CD4+ count (+59, p < 0.001) and CD4/CD8 ratio (+0.1, p < 0.001). As to metabolic parameters, we observed significant improvement in total cholesterol, tryglicerides and HDL cholesterol at both 240 and 480 weeks (p < 0.02 for all). Conclusion We assessed the efficacy and safety of DTG+3TC in the long term while also showing neutral impact on metabolic parameters. Disclosures All Authors: No reported disclosures
Source: Open Forum Infectious Diseases
Authors: Gianmaria Baldin, Arturo Ciccullo, Adriana Cervo, Letizia Oreni, Maria Mazzitelli, Filippo Lagi, Marianna Menozzi, Alberto Borghetti, Francesca Lombardi, Andrea Giacomelli, Massimiliano Fabbiani, Stefano Rusconi, Annamaria Cattelan, Spinello Antinori, Cristina Mussini, Simona Di Giambenedetto
Institutions: Agostino Gemelli University Polyclinic, Istituti di Ricovero e Cura a Carattere Scientifico, Azienda Ospedaliero-Universitaria di Modena, Luigi Sacco Hospital, ASST Fatebenefratelli Sacco, Azienda Ospedale - Università Padova, University of Florence, Azienda Ospedaliera Universitaria Pisana, University of Siena, Azienda Ospedaliera Universitaria Senese, University of Milan, Azienda Ospedaliera Ospedale Civile di Legnano, Aziende Socio Sanitarie Territoriale Ovest Milanese, University of Modena and Reggio Emilia
Language: English
Subfield: Infectious Diseases
Field: Medicine
Domain: Health Sciences
Open Access status: gold
Estimated APC paid: $4,053
OpenAlex ID: W7122686116
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