Literature DB >> 22951490

Pre-existing mutations in the rilpivirine Phase III trials ECHO and THRIVE: prevalence and impact on virological response.

Johan Vingerhoets1, Laurence Rimsky, Veerle Van Eygen, Steven Nijs, Simon Vanveggel, Katia Boven, Gaston Picchio.   

Abstract

BACKGROUND: Rilpivirine (RPV), a non-nucleoside reverse transcriptase inhibitor (NNRTI), was approved for HIV-1 infected, antiretroviral treatment-naive adults based on data from two Phase III trials. In the screening population, the prevalence of 49 NNRTI resistance-associated mutations (RAMs) and the impact of allowed NNRTI RAMs on virological response to an RPV- or efavirenz (EFV)-containing regimen were analysed.
METHODS: ECHO and THRIVE were global, Phase III, doubleblind, double-dummy, randomized trials in antiretroviral treatment-naive, HIV-1-infected adults to determine whether RPV 25 mg once daily had non-inferior efficacy versus EFV 600 mg once daily, both given with tenofovir/emtricitabine (ECHO) or tenofovir/emtricitabine, zidovudine/lamivudine or abacavir/lamivudine (THRIVE). The prevalence of 49 NNRTI RAMs, including the predefined list of 39 NNRTI RAMs used to exclude patients with potential resistance to RPV or EFV, was investigated at screening by population sequencing (including mixtures) using the virco(®)TYPE HIV-1 genotyping assay.
RESULTS: Of the 1,796 screened patients in whom genotypic resistance results were available, 372 (21%) had NNRTI RAMs. Of 527 screening failures, 148 (28%) were due to the presence of NNRTI RAMs. The presence of allowed NNRTI RAMs was associated with comparable response rates to the overall population (RPV 84.3% versus EFV 82.3%, intent-to-treat time-to-loss-of-virological-response): V90I (82.4% and 100% for RPV and EFV, respectively), V106I (85.7% and 93.3%), V179I (87.7% and 94.0%) and V189I (100.0% and 88.9%).
CONCLUSIONS: Analysis of the ECHO and THRIVE screened population suggests that transmitted NNRTI resistance is prevalent in treatment-naive patients but prevalence of the 15 RPV RAMs remains low. The four allowed NNRTI RAMs present at baseline did not affect RPV response at week 48.

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Year:  2012        PMID: 22951490     DOI: 10.3851/IMP2358

Source DB:  PubMed          Journal:  Antivir Ther        ISSN: 1359-6535


  10 in total

Review 1.  Burden of nonnucleoside reverse transcriptase inhibitor resistance in HIV-1-infected patients: a systematic review and meta-analysis.

Authors:  Sonya J Snedecor; Lavanya Sudharshan; Katherine Nedrow; Abhijeet Bhanegaonkar; Kit N Simpson; Seema Haider; Richard Chambers; Charles Craig; Jennifer Stephens
Journal:  AIDS Res Hum Retroviruses       Date:  2014-07-08       Impact factor: 2.205

2.  Sub-Epidemics Explain Localized High Prevalence of Reduced Susceptibility to Rilpivirine in Treatment-Naive HIV-1-Infected Patients: Subtype and Geographic Compartmentalization of Baseline Resistance Mutations.

Authors:  Kristof Theys; Kristel Van Laethem; Perpetua Gomes; Guy Baele; Andrea-Clemencia Pineda-Peña; Anne-Mieke Vandamme; Ricardo J Camacho; Ana B Abecasis
Journal:  AIDS Res Hum Retroviruses       Date:  2016-01-29       Impact factor: 2.205

3.  Quantifying Next Generation Sequencing Sample Pre-Processing Bias in HIV-1 Complete Genome Sequencing.

Authors:  Bram Vrancken; Nídia Sequeira Trovão; Guy Baele; Eric van Wijngaerden; Anne-Mieke Vandamme; Kristel van Laethem; Philippe Lemey
Journal:  Viruses       Date:  2016-01-07       Impact factor: 5.048

4.  Prevalence of Transmitted Drug-Resistance Mutations and Polymorphisms in HIV-1 Reverse Transcriptase, Protease, and gp41 Sequences Among Recent Seroconverters in Southern Poland.

Authors:  Joanna Smoleń-Dzirba; Magdalena Rosińska; Piotr Kruszyński; Jolanta Bratosiewicz-Wąsik; Robert Wojtyczka; Janusz Janiec; Bartosz Szetela; Marek Beniowski; Monika Bociąga-Jasik; Elżbieta Jabłonowska; Tomasz J Wąsik; And The Cascade Collaboration In EuroCoord
Journal:  Med Sci Monit       Date:  2017-02-07

5.  Frequent cross-resistance to rilpivirine among subtype C HIV-1 from first-line antiretroviral therapy failures in South Africa.

Authors:  Kerri J Penrose; Chanson J Brumme; Maritsa Scoulos-Hanson; Kristen Hamanishi; Kelley Gordon; Raquel V Viana; Carole L Wallis; P Richard Harrigan; John W Mellors; Urvi M Parikh
Journal:  Antivir Chem Chemother       Date:  2018 Jan-Dec

6.  Long-Acting Rilpivirine (RPV) Preexposure Prophylaxis Does Not Inhibit Vaginal Transmission of RPV-Resistant HIV-1 or Select for High-Frequency Drug Resistance in Humanized Mice.

Authors:  Kevin Melody; Chandra N Roy; Christopher Kline; Mackenzie L Cottrell; Dwayne Evans; Kathleen Shutt; Pleuni S Pennings; Brandon F Keele; Moses Bility; Angela D M Kashuba; Zandrea Ambrose
Journal:  J Virol       Date:  2020-03-31       Impact factor: 6.549

7.  Pre-existing singleton E138A mutations in the reverse transcriptase gene do not affect the efficacy of first-line antiretroviral therapy regimens using rilpivirine in human immunodeficiency virus-infected patients.

Authors:  Anna Kuznetsova; Aleksey Lebedev; Konstantin Gromov; Elena Kazennova; Maurizio Zazzi; Francesca Incardona; Anders Sönnerborg; Marina Bobkova
Journal:  Clin Case Rep       Date:  2022-02-03

Review 8.  An update on clinical utility of rilpivirine in the management of HIV infection in treatment-naïve patients.

Authors:  Opass Putcharoen; Stephen J Kerr; Kiat Ruxrungtham
Journal:  HIV AIDS (Auckl)       Date:  2013-09-16

9.  Transmitted drug resistance to rilpivirine among antiretroviral-naïve patients living with HIV from northern Poland.

Authors:  Miłosz Parczewski; Anna Urbańska; Katarzyna Maciejewska; Magdalena Witak-Jȩdra; Magdalena Leszczyszyn-Pynka
Journal:  J Int AIDS Soc       Date:  2014-04-17       Impact factor: 5.396

10.  Phase 2 Open-Label Study of Long-Term Safety, Tolerability, and Antiviral Activity of Rilpivirine in Antiretroviral-Naive Adolescents Living with HIV-1.

Authors:  Johan Lombaard; Francis Ssali; Puthanakit Thanyawee; Jan Fourie; Simon Vanveggel; Cornelia Linthicum; Veerle Van Eygen; Rodica Van Solingen-Ristea
Journal:  Antimicrob Agents Chemother       Date:  2021-12-06       Impact factor: 5.191

  10 in total

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