Evidence map›Paper›PMID 39436753›Full record

ArticleThe Journal of antimicrobial chemotherapy2025

Emergent resistance-associated mutations at first- or second-line HIV-1 virologic failure with second-generation InSTIs in two- and three-drug regimens: the Virostar-1 study.

Anne-Geneviève Marcelin, Cathia Soulie, Marc Wirden, Guillaume Barriere, François Durand, Charlotte Charpentier, Diane Descamps, Vincent Calvez

Abstract readMulticenter Study
In one paragraph

Article in The Journal of antimicrobial chemotherapy, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–field-weighted citation impact
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

11 citing papers in PubMed.

  1. Trial
  2. Observational
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  8. Review
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  10. Review
  11. Use of genotypic HIV DNA testing: a DELPHI-type consensus.The Journal of antimicrobial chemotherapy · 2024
    Article
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

8 authors.

Anne-Geneviève MarcelinSorbonne Université, INSERM, Pierre Louis Institute of Epidemiology and Public Health, AP-HP, Hôpital Pitié-Salpêtrière, Laboratoire de Virologie, Paris, France.
Cathia SoulieSorbonne Université, INSERM, Pierre Louis Institute of Epidemiology and Public Health, AP-HP, Hôpital Pitié-Salpêtrière, Laboratoire de Virologie, Paris, France.ORCID 0009-0008-2032-4148
Marc WirdenSorbonne Université, INSERM, Pierre Louis Institute of Epidemiology and Public Health, AP-HP, Hôpital Pitié-Salpêtrière, Laboratoire de Virologie, Paris, France.ORCID 0009-0003-3723-4142
Guillaume BarriereMedical Department, Gilead Sciences, S.A.S., Boulogne-Billancourt, France.ORCID 0009-0006-4776-4827
François DurandMedical Department, Gilead Sciences, S.A.S., Boulogne-Billancourt, France.
Charlotte CharpentierUniversité Paris Cité, INSERM, IAME, AP-HP, Hôpital Bichat-Claude Bernard, Laboratoire de Virologie, Paris, France.
Diane DescampsUniversité Paris Cité, INSERM, IAME, AP-HP, Hôpital Bichat-Claude Bernard, Laboratoire de Virologie, Paris, France.
Vincent CalvezSorbonne Université, INSERM, Pierre Louis Institute of Epidemiology and Public Health, AP-HP, Hôpital Pitié-Salpêtrière, Laboratoire de Virologie, Paris, France.

Funding

Gilead SciencesGilead Sciences Inc
6 · The paper itself

Abstract

backgroundSecond-generation integrase strand transfer inhibitors (InSTIs) have a high barrier to resistance and potent antiretroviral activity. They are recommended as first- or second-line (FL and SL) options in two- and three-drug regimens (2DR and 3DR) in international treatment guidelines. However, there are limited real-world data on emerging resistance at the time of virological failure (VF) with these regimens.

objectivesThe Virostar-1 study objective is to analyse the emergence of resistance-associated mutations (RAMs) over 3 years with DTG-based 2DRs and DTG- or bictegravir (BIC)-based 3DRs in people living with HIV (PLWH) experiencing a VF (FL or SL).

methodsRetrospective analysis of genotypic resistance detected at the time of a FL or SL VF with BIC/FTC/TAF, DTG/ABC/3TC, DTG/3TC and DTG/RPV between 2019 and 2022 was conducted from a French multicentre database. VF was defined as two consecutive HIV-1 plasma viral loads > 50 c/mL. Sanger assays were performed at VF within standard clinical care. Resistance mutations were reported using the ANRS algorithm. Selection biases prevent group comparisons.

resultsDuring the period, N = 5986 PLWH were followed either in FL or SL. The VF rate was overall low: BIC/FTC/TAF, 6.8%; DTG/ABC/3TC, 7.5%; DTG/3TC, 5.1%; and DTG/RPV, 2.1%. Some emergent InSTI or NRTI RAMs were detected with BIC/FTC/TAF 4%, DTG/ABC/3TC 8.5%, DTG/3TC 18% and 39% emergent NNRTI RAMs with DTG/RPV. However, a complete absence of dual resistance against NRTIs and InSTIs was observed.

conclusionsWe detected rare emergent InSTI RAMs and few emergent NRTI RAMs in PLWH failing DTG- or BIC-based regimens in FL or SL. The observed rates of emergent RAMs at VF were 4% with BIC/FTC/TAF, 8.5% with DTG/ABC/3TC, 18% with DTG/3TC and 39% with DTG/RPV.

Indexed as

Drug Resistance, ViralHIV-1HIV InfectionsMutationTreatment FailureAdultAmidesAnti-HIV AgentsDrug Therapy, CombinationFemaleGenotypeHeterocyclic Compounds, 3-RingHIV Integrase InhibitorsHumansMaleMiddle AgedAmidesAnti-HIV AgentsbictegravirHeterocyclic Compounds, 3-RingHIV Integrase InhibitorsPiperazinesPyridones

Identifiers

PMID39436753
PMCPMC11695916

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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.