Evidence map›Paper›PMID 26712907›Full record

ArticleThe Journal of antimicrobial chemotherapy2016

Dolutegravir-based monotherapy or dual therapy maintains a high proportion of viral suppression even in highly experienced HIV-1-infected patients.

Camelia Gubavu, Thierry Prazuck, Mohamadou Niang, Jennifer Buret, Catherine Mille, Jérôme Guinard, Véronique Avettand-Fènoël, Laurent Hocqueloux

Abstract read
In one paragraph

Article in The Journal of antimicrobial chemotherapy, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 2 pooled it
–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

21 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. A systematic review of the genetic mechanisms of dolutegravir resistance.The Journal of antimicrobial chemotherapy · 2019
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  7. Simplifying ARV Therapy in the Setting of Resistance.Current infectious disease reports · 2019
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Camelia GubavuService des Maladies Infectieuses et Tropicales, Centre Hospitalier Régional, Orléans, France.
Thierry PrazuckService des Maladies Infectieuses et Tropicales, Centre Hospitalier Régional, Orléans, France.
Mohamadou NiangService des Maladies Infectieuses et Tropicales, Centre Hospitalier Régional, Orléans, France.
Jennifer BuretService des Maladies Infectieuses et Tropicales, Centre Hospitalier Régional, Orléans, France.
Catherine MilleService des Maladies Infectieuses et Tropicales, Centre Hospitalier Régional, Orléans, France.
Jérôme GuinardLaboratoire de Virologie, Centre Hospitalier Régional, Orléans, France.
Véronique Avettand-FènoëlLaboratoire de Virologie, Hôpital Necker-Enfants Malades, APHP, Paris, France Université Paris-Descartes Sorbonne Paris Cité, Faculté de Médecine, EA 7327, Paris, France.
Laurent HocquelouxService des Maladies Infectieuses et Tropicales, Centre Hospitalier Régional, Orléans, France laurent.hocqueloux@chr-orleans.fr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDolutegravir is a powerful, well-tolerated integrase inhibitor with a high genetic barrier to resistance and may thus constitute the backbone of lightened regimens.

methodsThis was a monocentric, retrospective study. HIV-1-infected patients receiving dolutegravir as monotherapy (mDGV) or dual therapy (dDGV) were systematically identified. The primary outcome was the proportion of patients who maintained undetectable (<50 copies/mL) plasma HIV RNA [plasma viral load (PVL)].

resultsWe identified 21 patients on mDGV (50 mg/day) and 31 on dDGV (50 or 100 mg/day, with atazanavir  ±  ritonavir, n = 12; rilpivirine, n = 11; maraviroc, n = 3; lamivudine, n = 3; darunavir/ritonavir, n = 1; or abacavir, n = 1). All of the patients were treatment experienced and 48% had experienced at least one virological failure. The baseline characteristics were as follows (for the mDGV/dDGV patients, respectively): 5%/29% had a history of AIDS; the median (IQR) highest PVL was 4.5 (4.3-5.5)/5.3 (4.7-5.6) log copies/mL; the median (IQR) nadir CD4+ count was 310 (280-468)/199 (134-281) cells/mm(3); 100% had undetectable PVL before the mDGV for a median (IQR) duration of 5.9 (3.5-9.9) years/81% had undetectable PVL before the dDGV for a median (IQR) duration of 3.7 (1.4-8.3) years; and the median (IQR) HIV DNA level was 2.7 (2.1-3.1)/2.9 (2.7-3) log copies/10(6) PBMCs. At the last follow-up visit, 100% and 97% of patients showed undetectable PVL following mDGV and dDGV, respectively [median (IQR) follow-up of 32 (29-45) and 50 (30-74) weeks, respectively].

conclusionsIn our experience, dolutegravir-based lightened regimens provided a high proportion of viral suppression, even in highly treatment-experienced patients.

Indexed as

Viral LoadAnti-HIV AgentsAntiretroviral Therapy, Highly ActiveCD4 Lymphocyte CountDolutegravirDrug Resistance, ViralFemaleFollow-Up StudiesHeterocyclic Compounds, 3-RingHIV-1HIV InfectionsHumansMaleMiddle AgedMutationOxazinesAnti-HIV AgentsDolutegravirHeterocyclic Compounds, 3-RingOxazinesPiperazinesPyridones

Identifiers

PMID26712907
PMCPMC4790618

What OpenQuestion holds

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LicenceCC BY-NC
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Registered trials

None linked

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.