Evidence map›Paper›PMID 30544247›Full record

ArticleThe Journal of antimicrobial chemotherapy2019

Virological outcomes of boosted protease inhibitor-based first-line ART in subjects harbouring thymidine analogue-associated mutations as the sole form of transmitted drug resistance.

Anna Maria Geretti, Ellen White, Chloe Orkin, Anna Tostevin, Peter Tilston, David Chadwick, Clifford Leen, Caroline Sabin, David T Dunn, UK HIV Drug Resistance Database and UK CHIC Study

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of antimicrobial chemotherapy, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.0field-weighted citation impact, top 24% 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

3 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
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

10 authors at 7 institutions in 1 country.

Anna Maria GerettiInstitute of Infection & Global Health, University of Liverpool, Liverpool, UK.
Ellen WhiteMRC Clinical Trials Unit at University College London, London, UK.
Chloe OrkinDepartment of Infection & Immunity, Barts Health NHS Trust, London, UK.
Anna TostevinInstitute for Global Health, University College London, London, UK.
Peter TilstonDepartment of Clinical Virology, Manchester Royal Infirmary, Manchester, UK.
David ChadwickDepartment of Infectious Diseases, South Tees Hospitals NHS Trust, Middlesbrough, UK.
Clifford LeenRegional Infectious Diseases Unit, NHS Lothian, Edinburgh, UK.
Caroline SabinInstitute for Global Health, University College London, London, UK.
David T DunnInstitute for Global Health, University College London, London, UK.
UK HIV Drug Resistance Database and UK CHIC Study
University College London · GBSouth Tees Hospitals NHS Foundation Trust · GBBarts Health NHS Trust · GBManchester Royal Infirmary · GBNHS Lothian · GBUniversity of Liverpool · GBMRC Clinical Trials Unit at UCL · GB

Funding

Medical Research Council MC_U122886351Medical Research Council MC_UU_12023/15Medical Research Council MR/M004236/1
6 · The paper itself

Abstract

objectivesIn subjects with transmitted thymidine analogue mutations (TAMs), boosted PIs (PI/b) are often chosen to overcome possible resistance to the NRTI backbone. However, data to guide treatment selection are limited. Our aim was to obtain firmer guidance for clinical practice using real-world cohort data.

methodsWe analysed 1710 subjects who started a PI/b in combination with tenofovir or abacavir plus emtricitabine or lamivudine, and compared their virological outcomes with those of 4889 patients who started an NNRTI (predominantly efavirenz), according to the presence of ≥1 TAM as the sole form of transmitted drug resistance.

resultsParticipants with ≥1 TAM comprised predominantly MSM (213 of 269, 79.2%), subjects of white ethnicity (206 of 269, 76.6%) and HIV-1 subtype B infections (234 of 269, 87.0%). Most (203 of 269, 75.5%) had singleton TAMs, commonly a revertant of T215Y or T215F (112 of 269, 41.6%). Over a median of 2.5 years of follow-up, 834 of 6599 (12.6%) subjects experienced viraemia (HIV-1 RNA >50 copies/mL). The adjusted HR for viraemia was 2.17 with PI/b versus NNRTI-based therapy (95% CI 1.88-2.51; P < 0.001). Other independent predictors of viraemia included injecting drug use, black ethnicity, higher viral load and lower CD4 cell count at baseline, and receiving abacavir instead of tenofovir. Resistance showed no overall impact (adjusted HR 0.77 with ≥1 TAM versus no resistance; 95% CI 0.54-1.10; P = 0.15).

conclusionsIn this cohort, patients harbouring ≥1 TAM as the sole form of transmitted drug resistance gained no apparent virological advantage from starting first-line ART with a PI/b.

Indexed as

Drug Resistance, ViralMutationAdultAllelesAmino Acid SubstitutionAnti-HIV AgentsAntiretroviral Therapy, Highly ActiveFemaleGenotypeHIV-1HIV InfectionsHumansKaplan-Meier EstimateMalePrognosisProtease InhibitorsAnti-HIV AgentsProtease InhibitorsRNA, Viral

Identifiers

PMID30544247
PMCPMC6376847
OpenAlexW2913665820

What OpenQuestion holds

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LicenceCC BY-NC
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.