1. Real world effectiveness of standard of care triple therapy versus two-drug combinations for treatment of people living with HIV
- Author
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Universitat Rovira i Virgili, Teira, Ramon; Diaz-Cuervo, Helena; Aragao, Filipa; Marguet, Sophie; de la Fuente, Belen; Jose Munoz, Maria; Abdulghani, Nadia; Ribera, Esteban; Domingo, Pere; Deig, Elisabeth; Peraire, Joaquim; Roca, Bernardino; Montero, Marta; Jose Galindo, Maria; Romero, Alberto; Espinosa, Nuria; Lozano, Fernando; Dolores Merino, Maria; Martinez, Elisa; Geijo, Paloma; Estrada, Vicente; Garcia, Josefina; Antonia Sepulveda, M.; Berenguer, Juan, Universitat Rovira i Virgili, and Teira, Ramon; Diaz-Cuervo, Helena; Aragao, Filipa; Marguet, Sophie; de la Fuente, Belen; Jose Munoz, Maria; Abdulghani, Nadia; Ribera, Esteban; Domingo, Pere; Deig, Elisabeth; Peraire, Joaquim; Roca, Bernardino; Montero, Marta; Jose Galindo, Maria; Romero, Alberto; Espinosa, Nuria; Lozano, Fernando; Dolores Merino, Maria; Martinez, Elisa; Geijo, Paloma; Estrada, Vicente; Garcia, Josefina; Antonia Sepulveda, M.; Berenguer, Juan
- Abstract
BackgroundSince 1996, the standard of care (SOC) therapy for HIV treatment has consisted of a backbone of two nucleoside analogue reverse transcriptase inhibitors (NRTI) paired with a third agent. Use of two-drug combinations (2DC) has been considered for selected patients to avoid toxicities associated with the use of NRTIs. This study aimed to compare the real-world outcomes of integrase strand transfer inhibitor (INSTI)-containing triple therapy (TT) to dolutegravir- (DTG) and/or boosted protease inhibitor (bPI)-based 2DC in a large Spanish cohort of HIV patients.MethodsA retrospective analysis was performed using data from the VACH cohort, a prospective multicentre Spanish cohort of adult HIV patients. All treatment experienced patients initiating a TT of an INSTI combined with two NRTIs or a 2DC-containing DTG and/or a bPI between 01/01/2012 and 01/06/2017 were included. The unit of analysis was patient-regimens. The overall sample analysis was complemented with two sub-analyses. The first sub-analysis focused on patients treated with a backbone plus DTG compared to those treated with DTG+ one other antiretroviral. The second sub-analysis focused on patients with HIV RNA<50 copies/mL at baseline, irrespective of the regimen used. The following endpoints were assessed: time to discontinuation for any reason, time to switch due to virologic failure, and time to switch due to toxicity (reasons for discontinuation according to clinician report in the database). Time-to-event analyses were conducted using Kaplan-Meier survival curves and Cox regression models.ResultsOverall 7,481 patients were included in the analysis, contributing to 9,243 patient-regimens. Patient characteristics at baseline differed among groups, with the 2DC group being significantly older and havin
- Published
- 2021