Literature DB >> 28186251

Switch as maintenance to elvitegravir/cobicistat/emtricitabine/tenofovir disoproxil fumarate: week 48 results in a clinical cohort.

Marine Perrier1,2, Charlotte Charpentier1,2, Gilles Peytavin1,3,4, Minh Lê1,3,4, Louis Blondel4, Benoit Visseaux1,2, Véronique Joly1,3,5, Adriana Pinto5, Sophie Matheron1,3,5, Yazdan Yazdanpanah1,3,5, Diane Descamps1,2, Roland Landman1,3,5.   

Abstract

Objectives: To assess, in a clinical cohort, the efficacy of switching current ART in virologically suppressed patients to elvitegravir/cobicistat/emtricitabine/tenofovir disoproxil fumarate as a single-tablet regimen (STR) using the PCR signal of the plasma viral load (pVL) assay and determination of plasma drug concentration ( C 24 ). Patients and methods: This was an observational single-centre study enrolling antiretroviral-treated patients with pVL <50 copies/mL initiating elvitegravir-based STR. PCRneg was defined as an undetected PCR signal.
Results: One hundred and fifty-one patients were enrolled. At STR baseline, the median time since first ART and time of virological suppression were 5 years (IQR 3-9) and 24 months (IQR 9-44), respectively. By week (W) 48, 26 (17%) of the patients had discontinued STR due to adverse events. The proportion of patients maintaining pVL <50 copies/mL on treatment was 98%, 96%, 93% and 97% at W12, W24, W36 and W48, respectively. Five patients (3.3%) experienced a virological failure and emergence of resistance was observed in two of them with the selection of M184V and N155H mutations. At baseline, W12, W24, W36 and W48, 70%, 57%, 72%, 61% and 74% of the patients with pVL <20 copies/mL had a PCRneg, respectively. The median elvitegravir plasma C 24 value was 648 ng/mL (IQR 348-989; n  =   237), with 84% of elvitegravir C 24 values >45 ng/mL, the protein-adjusted IC 95 . Conclusions: In this clinical cohort of virologically suppressed patients switching to STR, most subjects had adequate elvitegravir C 24 values with a high proportion maintaining virological suppression with no residual viraemia until W48.
© The Author 2017. Published by Oxford University Press on behalf of the British Society for Antimicrobial Chemotherapy. All rights reserved. For Permissions, please email: journals.permissions@oup.com.

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Year:  2017        PMID: 28186251     DOI: 10.1093/jac/dkx018

Source DB:  PubMed          Journal:  J Antimicrob Chemother        ISSN: 0305-7453            Impact factor:   5.790


  3 in total

1.  Effectiveness of integrase strand transfer inhibitors among treatment-experienced patients in a clinical setting.

Authors:  Thibaut Davy-Mendez; Sonia Napravnik; Oksana Zakharova; David A Wohl; Claire E Farel; Joseph J Eron
Journal:  AIDS       Date:  2019-06-01       Impact factor: 4.177

Review 2.  Simplifying ARV Therapy in the Setting of Resistance.

Authors:  Neha Sheth Pandit; Daniel B Chastain; Andrea M Pallotta; Melissa E Badowski; Emily C Huesgen; Sarah M Michienzi
Journal:  Curr Infect Dis Rep       Date:  2019-09-07       Impact factor: 3.725

3.  Optimizing Antiretroviral Therapy in Treatment-Experienced Patients Living with HIV: A Critical Review of Switch and Simplification Strategies. An Opinion of the HIV Practice and Research Network of the American College of Clinical Pharmacy.

Authors:  Daniel Chastain; Melissa Badowski; Emily Huesgen; Neha Sheth Pandit; Andrea Pallotta; Sarah Michienzi
Journal:  J Int Assoc Provid AIDS Care       Date:  2019 Jan-Dec
  3 in total

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