Evidence map›Paper›PMID 33409332›Full record

ArticleOpen forum infectious diseases2020

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.

Hélène Chaussade, Camille Tumiotto, Fabien Le Marec, Olivier Leleux, Lucile Lefèvre, Estibaliz Lazaro, Marie-Edith Lafon, Elsa Nyamankolly, Pierre Duffau, Didier Neau and 2 more

Open access · goldAbstract read
In one paragraph

Article in Open forum infectious diseases, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.1field-weighted citation impact, top 51% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 3 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 4 institutions in 1 country.

Hélène ChaussadeCHU Bordeaux, Services de Médecine Interne et Maladies Infectieuses, Bordeaux, France.
Camille TumiottoCHU Bordeaux, Virology Laboratory, Bordeaux, France.
Fabien Le MarecUniv. Bordeaux, ISPED, Inserm, Bordeaux Population Health Research Center, Team MORPH3Eus, UMR, Bordeaux, France.
Olivier LeleuxUniv. Bordeaux, ISPED, Inserm, Bordeaux Population Health Research Center, Team MORPH3Eus, UMR, Bordeaux, France.
Lucile LefèvreJANSSEN France, Issy-les-Moulineaux, France.
Estibaliz LazaroCHU Bordeaux, Services de Médecine Interne et Maladies Infectieuses, Pessac, France.
Marie-Edith LafonCHU Bordeaux, Virology Laboratory, Bordeaux, France.
Elsa NyamankollyCHU Bordeaux, Service des Maladies Infectieuses et Tropicales, Bordeaux, France.
Pierre DuffauCHU Bordeaux, Services de Médecine Interne et Maladies Infectieuses, Bordeaux, France.
Didier NeauCHU Bordeaux, Service des Maladies Infectieuses et Tropicales, Bordeaux, France.
Pantxika BellecaveCHU Bordeaux, Virology Laboratory, Bordeaux, France.
Fabrice BonnetCHU Bordeaux, Services de Médecine Interne et Maladies Infectieuses, Bordeaux, France.
Centre Hospitalier Universitaire de Bordeaux · FRInserm · FRJanssen (France) · FRUniversité de Bordeaux · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRitonavir-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.

methodsData 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).

resultsAmong 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.

conclusionsThese 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.

Indexed as

darunavirgenotypeHIV-1mutation rate

Identifiers

PMID33409332
PMCPMC7772944
OpenAlexW3106966184

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.