Evidence map›Paper›PMID 30270543›Full record

Trial reportHIV medicine2019

Predictors of virological failure in HIV-1-infected patients switching to dolutegravir maintenance monotherapy.

Iea Wijting, S L Rutsaert, C Rokx, D M Burger, A Verbon, Jja van Kampen, Cab Boucher, Bja Rijnders, L Vandekerckhove

Registry-linked trialAbstract readEquivalence TrialRandomized Controlled Trial
In one paragraph

Trial report in HIV medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02401828 (The Dolutegravir Antiretroviral Mono-Therapy for HIV Trial), which is not on this map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 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.

NCT02401828 phase4completednot on this map

The Dolutegravir Antiretroviral Mono-Therapy for HIV Trial

TypeinterventionalSponsorErasmus Medical CenterRan2015 to 2017Enrolled134ConditionsHuman Immunodeficiency VirusArmsDolutegravir
3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. A systematic review of the genetic mechanisms of dolutegravir resistance.The Journal of antimicrobial chemotherapy · 2019
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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

9 authors.

Iea WijtingDepartment of Internal Medicine, Infectious Diseases, Erasmus University Medical Center, Rotterdam, The Netherlands.ORCID 0000-0002-7077-9887
S L RutsaertDepartment of Internal Medicine, HIV Cure Research Center, Ghent University, Ghent, Belgium.
C RokxDepartment of Internal Medicine, Infectious Diseases, Erasmus University Medical Center, Rotterdam, The Netherlands.
D M BurgerDepartment of Pharmacy, Radboud University Medical Center, Nijmegen, The Netherlands.
A VerbonDepartment of Internal Medicine, Infectious Diseases, Erasmus University Medical Center, Rotterdam, The Netherlands.
Jja van KampenDepartment of Viroscience, Erasmus University Medical Center, Rotterdam, The Netherlands.
Cab BoucherDepartment of Viroscience, Erasmus University Medical Center, Rotterdam, The Netherlands.
Bja RijndersDepartment of Internal Medicine, Infectious Diseases, Erasmus University Medical Center, Rotterdam, The Netherlands.
L VandekerckhoveDepartment of Internal Medicine, HIV Cure Research Center, Ghent University, Ghent, Belgium.

Funding

Erasmus University Rotterdam Trustfund 97030.34/15
6 · The paper itself

Abstract

objectivesThe Dolutegravir Monotherapy for HIV (DOMONO; NCT02401828) study showed that maintenance monotherapy with dolutegravir (DTG) is associated with virological failure (VF) and leads to DTG resistance and as a result should not be used. However, data on clinical and virological factors associated with VF during DTG monotherapy are lacking. We identified factors associated with VF during DTG monotherapy.

methodsA randomized trial was carried out in which patients on combination antiretroviral therapy (cART) with an HIV-1 RNA zenith < 100 000 copies/mL and a CD4 T-cell nadir ≥ 200 cells/μL, who had never experienced VF, switched to DTG monotherapy. Clinical and virological factors were compared between patients with and without VF, using univariate analyses.

resultsEight of the 95 patients developed VF during DTG monotherapy. A total of 78 participants had reached week 48 when the study was discontinued. The median CD4 T-cell nadir was lower in patients with VF than in patients without VF [260 (interquartile range (IQR) 223-320) versus 380 (IQR 290-520) cells/μL, respectively; P = 0.011]. Patients with VF had a longer time between HIV diagnosis and cART initiation than those without VF [median 49 (IQR 27-64) versus 15 (IQR 1-38) months, respectively; P = 0.015]. The median total peripheral blood mononuclear cell (PBMC) HIV DNA copy number was higher in patients with VF than in those without VF [417 (range 85-4151) versus 147 (range 16-4132) copies/10

conclusionsA lower CD4 nadir, a longer time between HIV diagnosis and cART initiation, and a higher HIV DNA copy number at the time of DTG monotherapy initiation were associated with VF. While there clearly is no future role for DTG monotherapy, ongoing and future studies on the efficacy of maintenance dual therapy (e.g. DTG lamivudine) may have to take these variables into account in their study design and analysis.

Indexed as

AdultCD4 Lymphocyte CountDolutegravirFemaleHeterocyclic Compounds, 3-RingHIV-1HIV InfectionsHIV Integrase InhibitorsHumansMaintenance ChemotherapyMaleMiddle AgedOxazinesPiperazinesPyridonesTreatment FailureDolutegravirHeterocyclic Compounds, 3-RingHIV Integrase InhibitorsOxazinesPiperazinesPyridonescombination antiretroviral therapydolutegravir monotherapyHIV-1HIV integrase inhibitorsvirological failure

Identifiers

PMID30270543
PMCPMC6586017

What OpenQuestion holds

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Registered trials

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.