TY - JOUR
T1 - Long-term use of darunavir/ritonavir-containing regimens in daily practice in Belgium: retrospective observational cohort data of 1701 HIV-patients
AU - BREACH Consortium
AU - De Wit, Stephane
AU - Florence, Eric
AU - Vandekerckhove, Linos
AU - Vandercam, Bernard
AU - Goffard, Jean-Christophe
AU - Van Wijngaerden, Eric
AU - Moutschen, Michel
AU - Demeester, Remy
AU - Thilakarathne, Pushpike
AU - Piryns, Hilde
N1 - FTX
PY - 2018
Y1 - 2018
N2 - Background Once daily (QD) ritonavir or cobicistat-boosted darunavir (DRV/b), in combination with other antiretrovirals (ARVs), is recommended as a first-line option for human immunodeficiency virus-infected patients in European and USA guidelines. The objective of this study was to analyse the outcomes of DRV/r QD-based antiretroviral therapy (ART) regimens in real-life settings.Methods This is an observational, non-interventional, non-comparative, retrospective, multicentre cohort study. Data were collected from the databases of eight Belgian AIDS Reference Centres. All patients who received at least one dose of DRV/r QD, regardless of background ARV regimen, with a minimum follow-up of 6months were included.Results Data from 1701 subjects were collected. Most were male (66.5%) with a mean age of 42.9years, 33.1% were treatment-naive and 66.9% were ART experienced. During a median follow-up of 2.45years (95% CI: 1.50-3.34), the probability to remain on treatment was 87% for the first year, 79% for the second year. DRV/r was well tolerated with few discontinuations due to adverse events (6.9%) or virological failure (0.8%). Among the 1138 treatment-experienced patients, 111 (9.8%) patients received DRV/r QD monotherapy.Conclusions This retrospective cohort analysis confirms the long-term effectiveness and good tolerability of DRV/r QD in a real-life setting. No unexpected adverse events were reported.
AB - Background Once daily (QD) ritonavir or cobicistat-boosted darunavir (DRV/b), in combination with other antiretrovirals (ARVs), is recommended as a first-line option for human immunodeficiency virus-infected patients in European and USA guidelines. The objective of this study was to analyse the outcomes of DRV/r QD-based antiretroviral therapy (ART) regimens in real-life settings.Methods This is an observational, non-interventional, non-comparative, retrospective, multicentre cohort study. Data were collected from the databases of eight Belgian AIDS Reference Centres. All patients who received at least one dose of DRV/r QD, regardless of background ARV regimen, with a minimum follow-up of 6months were included.Results Data from 1701 subjects were collected. Most were male (66.5%) with a mean age of 42.9years, 33.1% were treatment-naive and 66.9% were ART experienced. During a median follow-up of 2.45years (95% CI: 1.50-3.34), the probability to remain on treatment was 87% for the first year, 79% for the second year. DRV/r was well tolerated with few discontinuations due to adverse events (6.9%) or virological failure (0.8%). Among the 1138 treatment-experienced patients, 111 (9.8%) patients received DRV/r QD monotherapy.Conclusions This retrospective cohort analysis confirms the long-term effectiveness and good tolerability of DRV/r QD in a real-life setting. No unexpected adverse events were reported.
KW - Belgium
KW - HAART (highly active antiretroviral therapy)
KW - HIV (human immunodeficiency virus)
KW - darunavir
KW - once-daily
KW - REVERSE-TRANSCRIPTASE INHIBITORS
KW - ROUTINE CLINICAL-PRACTICE
KW - EXPERIENCED PATIENTS
KW - NUCLEOSIDE ANALOGS
KW - OPEN-LABEL
KW - EFFICACY
KW - MONOTHERAPY
KW - NAIVE
KW - TRIAL
KW - SAFETY
U2 - 10.1080/17843286.2018.1458428
DO - 10.1080/17843286.2018.1458428
M3 - A1: Web of Science-article
SN - 1784-3286
VL - 73
SP - 341
EP - 347
JO - Acta Clinica Belgica
JF - Acta Clinica Belgica
IS - 5
ER -