Evidence map›Paper›PMID 38543764›Full record

ArticleViruses2024

Prevalence of Emergent Dolutegravir Resistance Mutations in People Living with HIV: A Rapid Scoping Review.

Carolyn Chu, Kaiming Tao, Vinie Kouamou, Ava Avalos, Jake Scott, Philip M Grant, Soo-Yon Rhee, Suzanne M McCluskey, Michael R Jordan, Rebecca L Morgan and 1 more

Open access · goldAbstract readScoping Review
In one paragraph

Article in Viruses, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed, 1 pooled it
19.1field-weighted citation impact, top 1% 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

42 citing papers in PubMed, 1 synthesis or guideline pooled it, 49 citations in OpenAlex.

  1. Virologic Failure and Emergent Integrase Strand Transfer Inhibitor Drug Resistance With Long-Acting Cabotegravir for HIV Treatment: A Meta-analysis.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2025
    Pooled it
  2. Trial
  3. Trial
  4. A Real-Time Urine Tenofovir Assay Improves Drug Adherence Among People With HIV With Prior Virologic Failure in a Randomized Controlled Trial.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2025
    Trial
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. HIV Resistance to Dolutegravir Varies With Coadministered Agents.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2026
    Article
  13. Article
  14. Article
  15. Approaches to the Management of Virologic Failure on Dolutegravir-Based Antiretroviral Therapy in the 50 Countries With the Highest Adult HIV Prevalence.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2026
    Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

11 authors at 6 institutions in 2 countries.

Carolyn ChuDepartment of Family and Community Medicine, University of California San Francisco, San Francisco, CA 94110, USA.
Kaiming TaoDivision of Infectious Diseases, Department of Medicine, Stanford University, Stanford, CA 94305, USA.
Vinie KouamouFaculty of Medicine and Health Sciences, University of Zimbabwe, Harare 00263, Zimbabwe.ORCID 0000-0003-3531-7780
Ava AvalosCareena Center for Health, Gaborone, Botswana.ORCID 0000-0003-4111-7072
Jake ScottDivision of Infectious Diseases, Department of Medicine, Stanford University, Stanford, CA 94305, USA.ORCID 0000-0003-4210-509X
Philip M GrantDivision of Infectious Diseases, Department of Medicine, Stanford University, Stanford, CA 94305, USA.
Soo-Yon RheeDivision of Infectious Diseases, Department of Medicine, Stanford University, Stanford, CA 94305, USA.
Suzanne M McCluskeyDivision of Infectious Diseases, Harvard Medical School, Boston, MA 02115, USA.
Michael R JordanDivision of Geographic Medicine and Infectious Diseases, Tufts Medical Center, Boston, MA 02111, USA.
Rebecca L MorganSchool of Medicine, Case Western Reserve University, Cleveland, OH 44106, USA.
Robert W ShaferDivision of Infectious Diseases, Department of Medicine, Stanford University, Stanford, CA 94305, USA.ORCID 0000-0003-2513-2643
Stanford University · USCase Western Reserve University · USHarvard University · USTufts University · USUniversity of California, San Francisco · USUniversity of Zimbabwe · ZW

Funding

HIV Drug Resistance DatabaseR24AI136618 · NIAID · STANFORD UNIVERSITY · PI ROBERT William SHAFER · 2018 to 2026
$7.3M
NIAID NIH HHS R24 AI136618NIH HHS 2R24AI13661806
6 · The paper itself

Abstract

backgroundDolutegravir (DTG) is a cornerstone of global antiretroviral (ARV) therapy (ART) due to its high efficacy and favorable tolerability. However, limited data exist regarding the risk of emergent integrase strand transfer inhibitor (INSTI) drug-resistance mutations (DRMs) in individuals receiving DTG-containing ART.

methodsWe performed a PubMed search using the term "Dolutegravir", last updated 18 December 2023, to estimate the prevalence of VF with emergent INSTI DRMs in people living with HIV (PLWH) without previous VF on an INSTI who received DTG-containing ART.

resultsOf 2131 retrieved records, 43 clinical trials, 39 cohorts, and 6 cross-sectional studies provided data across 6 clinical scenarios based on ART history, virological status, and co-administered ARVs: (1) ART-naïve PLWH receiving DTG plus two NRTIs; (2) ART-naïve PLWH receiving DTG plus lamivudine; (3) ART-experienced PLWH with VF on a previous regimen receiving DTG plus two NRTIs; (4) ART-experienced PLWH with virological suppression receiving DTG plus two NRTIs; (5) ART-experienced PLWH with virological suppression receiving DTG and a second ARV; and (6) ART-experienced PLWH with virological suppression receiving DTG monotherapy. The median proportion of PLWH in clinical trials with emergent INSTI DRMs was 1.5% for scenario 3 and 3.4% for scenario 6. In the remaining four trial scenarios, VF prevalence with emergent INSTI DRMs was ≤0.1%. Data from cohort studies minimally influenced prevalence estimates from clinical trials, whereas cross-sectional studies yielded prevalence data lacking denominator details.

conclusionsIn clinical trials, the prevalence of VF with emergent INSTI DRMs in PLWH receiving DTG-containing regimens has been low. Novel approaches are required to assess VF prevalence with emergent INSTI DRMs in PLWH receiving DTG in real-world settings.

Indexed as

Anti-HIV AgentsHIV InfectionsHIV Integrase InhibitorsOxazinesPiperazinesPyridonesCross-Sectional StudiesDolutegravirHeterocyclic Compounds, 3-RingHumansLamivudineMutationPrevalenceAnti-HIV AgentsDolutegravirHeterocyclic Compounds, 3-RingHIV Integrase InhibitorsLamivudineOxazinesPiperazinesPyridonesepidemiologyHIVsystematic reviewtreatment

Identifiers

PMID38543764
PMCPMC10975848
OpenAlexW4392378382

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.