A Low Level of Darunavir Resistance-Associated Mutation Emergence in Patients With Virological Failure During Long-term Use of Darunavir in People With HIV. The ANRS CO3 Aquitaine Cohort.

HIV-1 darunavir genotype mutation rate

Journal

Open forum infectious diseases
ISSN: 2328-8957
Titre abrégé: Open Forum Infect Dis
Pays: United States
ID NLM: 101637045

Informations de publication

Date de publication:
Dec 2020
Historique:
received: 07 09 2020
accepted: 18 11 2020
entrez: 7 1 2021
pubmed: 8 1 2021
medline: 8 1 2021
Statut: epublish

Résumé

Ritonavir-boosted darunavir (DRV/r) is a protease inhibitor (PI) indicated for the treatment of naïve and pretreated HIV-infected patients since 2007. Our study aims to describe DRV/r-treated patients experiencing virological failure (VF) documented with HIV resistance testing. Data from patients belonging to the ANRS CO3 Aquitaine Cohort treated with a regimen including DRV/r between February 2007 and December 2015 were analyzed. Baseline characteristics of patients experiencing VF (defined by 2 consecutive plasma viral loads >50 copies/mL) were compared with those without VF. We then described factors associated with VF as emergence of IAS DRV resistance-associated mutations (RAMs). Among the 1458 patients treated at least once with a DRV/r-based regimen, 270 (18.5%) patients experienced VF during follow-up, including 240 with at least 1 genotype resistance test (GRT). DRV RAMs were detected in 29 patients (12%). Among them, 25/29 patients had ≥2 DRV RAMs before DRV/r initiation, all of whom had experienced VF during previous PI treatments. For 18/29, DRV/r was maintained after VF, and controlled viremia was restored after modification of DRV-associated antiretroviral molecules or increased DRV dose. Finally, only 6/29 patients selected new DRV RAMs after DRV/r initiation. All of these experienced previous VFs while on other PIs. These results highlight the efficacy and robustness of DRV/r, as the emergence of DRV RAMs appeared in <0.4% of patients receiving a DRV/r-based regimen in our large cohort.

Sections du résumé

BACKGROUND BACKGROUND
Ritonavir-boosted darunavir (DRV/r) is a protease inhibitor (PI) indicated for the treatment of naïve and pretreated HIV-infected patients since 2007. Our study aims to describe DRV/r-treated patients experiencing virological failure (VF) documented with HIV resistance testing.
METHODS METHODS
Data from patients belonging to the ANRS CO3 Aquitaine Cohort treated with a regimen including DRV/r between February 2007 and December 2015 were analyzed. Baseline characteristics of patients experiencing VF (defined by 2 consecutive plasma viral loads >50 copies/mL) were compared with those without VF. We then described factors associated with VF as emergence of IAS DRV resistance-associated mutations (RAMs).
RESULTS RESULTS
Among the 1458 patients treated at least once with a DRV/r-based regimen, 270 (18.5%) patients experienced VF during follow-up, including 240 with at least 1 genotype resistance test (GRT). DRV RAMs were detected in 29 patients (12%). Among them, 25/29 patients had ≥2 DRV RAMs before DRV/r initiation, all of whom had experienced VF during previous PI treatments. For 18/29, DRV/r was maintained after VF, and controlled viremia was restored after modification of DRV-associated antiretroviral molecules or increased DRV dose. Finally, only 6/29 patients selected new DRV RAMs after DRV/r initiation. All of these experienced previous VFs while on other PIs.
CONCLUSIONS CONCLUSIONS
These results highlight the efficacy and robustness of DRV/r, as the emergence of DRV RAMs appeared in <0.4% of patients receiving a DRV/r-based regimen in our large cohort.

Identifiants

pubmed: 33409332
doi: 10.1093/ofid/ofaa567
pii: ofaa567
pmc: PMC7772944
doi:

Types de publication

Journal Article

Langues

eng

Pagination

ofaa567

Informations de copyright

© The Author(s) 2020. Published by Oxford University Press on behalf of Infectious Diseases Society of America.

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Auteurs

Hélène Chaussade (H)

CHU Bordeaux, Services de Médecine Interne et Maladies Infectieuses, Bordeaux, France.

Camille Tumiotto (C)

CHU Bordeaux, Virology Laboratory, Bordeaux, France.

Fabien Le Marec (F)

Univ. Bordeaux, ISPED, Inserm, Bordeaux Population Health Research Center, Team MORPH3Eus, UMR, Bordeaux, France.

Olivier Leleux (O)

Univ. Bordeaux, ISPED, Inserm, Bordeaux Population Health Research Center, Team MORPH3Eus, UMR, Bordeaux, France.

Lucile Lefèvre (L)

JANSSEN France, Issy-les-Moulineaux, France.

Estibaliz Lazaro (E)

CHU Bordeaux, Services de Médecine Interne et Maladies Infectieuses, Pessac, France.

Marie-Edith Lafon (ME)

CHU Bordeaux, Virology Laboratory, Bordeaux, France.

Elsa Nyamankolly (E)

CHU Bordeaux, Service des Maladies Infectieuses et Tropicales, Bordeaux, France.

Pierre Duffau (P)

CHU Bordeaux, Services de Médecine Interne et Maladies Infectieuses, Bordeaux, France.

Didier Neau (D)

CHU Bordeaux, Service des Maladies Infectieuses et Tropicales, Bordeaux, France.

Pantxika Bellecave (P)

CHU Bordeaux, Virology Laboratory, Bordeaux, France.

Fabrice Bonnet (F)

CHU Bordeaux, Services de Médecine Interne et Maladies Infectieuses, Bordeaux, France.
Univ. Bordeaux, ISPED, Inserm, Bordeaux Population Health Research Center, Team MORPH3Eus, UMR, Bordeaux, France.

Classifications MeSH