Long-term use of darunavir/ritonavir-containing regimens in daily practice in Belgium: retrospective observational cohort data of 1701 HIV-patients

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    Abstract

    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.

    Original languageEnglish
    JournalActa Clinica Belgica
    Volume73
    Issue number5
    Pages (from-to)341-347
    Number of pages7
    ISSN1784-3286
    DOIs
    Publication statusPublished - 2018

    Keywords

    • Belgium
    • HAART (highly active antiretroviral therapy)
    • HIV (human immunodeficiency virus)
    • darunavir
    • once-daily
    • REVERSE-TRANSCRIPTASE INHIBITORS
    • ROUTINE CLINICAL-PRACTICE
    • EXPERIENCED PATIENTS
    • NUCLEOSIDE ANALOGS
    • OPEN-LABEL
    • EFFICACY
    • MONOTHERAPY
    • NAIVE
    • TRIAL
    • SAFETY

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