Evidence map›Paper›PMID 29352723›Full record

Trial reportThe lancet. HIV2018

Which HIV-infected adults with high CD4 T-cell counts benefit most from immediate initiation of antiretroviral therapy? A post-hoc subgroup analysis of the START trial.

Jean-Michel Molina, Birgit Grund, Fred Gordin, Ian Williams, Mauro Schechter, Marcello Losso, Matthew Law, Ernest Ekong, Noluthando Mwelase, Athanasios Skoutelis and 7 more

2 registry-linked trialsOpen access · bronzeAbstract readComparative StudyMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in The lancet. HIV, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
3.5field-weighted citation impact, top 7% 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.

NCT00867048 phase4completednot on this map

Strategic Timing of AntiRetroviral Treatment

TypeinterventionalSponsorUniversity of MinnesotaRan2009 to 2022Enrolled4,688ConditionsHIV InfectionArmsAll licensed antiretroviral medications
NCT03723525 phase4completednot on this map

Evaluation of World Health Organization (WHO) Recommendations on Test and Treat Strategy, Managing Advanced HIV Disease and Rapid Initiation of ART Among People Living With HIV in Nepal: A Cluster Randomized Trial.

TypeinterventionalSponsorNational Centre for AIDs and STD Control, NepalRan2018 to 2019Enrolled1,073ConditionsHIVArmsPackage of HIV care, Standard HIV care
3 · Its place in the literature

Who cites it

18 citing papers in PubMed, 36 citations in OpenAlex.

  1. ART in HIV-Positive Persons With Low Pretreatment Viremia: Results From the START Trial.Journal of acquired immune deficiency syndromes (1999) · 2019
    Trial
  2. Trial
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Frailty in People Living with HIV.Current HIV/AIDS reports · 2020
    Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. The Benefits of Immediate ART.Journal of the International Association of Providers of AIDS Care
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 14 institutions in 11 countries.

Jean-Michel MolinaUniversity of Paris Diderot, Sorbonne Paris Cité, Saint-Louis Hospital, Assistance Publique Hôpitaux de Paris, Agence Nationale de Recherches sur le SIDA et les Hépatites Virales (ANRS), Paris, France. Electronic address: jean-michel.molina@aphp.fr.
Birgit GrundSchool of Statistics, University of Minnesota, Minneapolis, MN, USA.
Fred GordinWashington Veterans Affairs Medical Center, George Washington University, Washington, DC, USA.
Ian WilliamsUniversity College London Medical School, London, UK.
Mauro SchechterProjeto Praça Onze, Universidade Federal do Rio de Janeiro, Brazil.
Marcello LossoHospital General de Agudos JM Ramos, Buenos Aeres, Argentina.
Matthew LawKirby Institute, University of New South Wales, Sydney, NSW, Australia.
Ernest EkongInstitute of Human Virology, Abuja, Nigeria.
Noluthando MwelaseDepartment of Medicine, University of Witwatersrand, Johannesburg, South Africa.
Athanasios SkoutelisEvanlegismos General Hospital, Athens, Greece.
Martin J WiselkaLeicester Royal Infirmary, Leicester, UK.
Linos VandekerckhoveUniversitaire Ziekenhuizen Gent, Ghent, Belgium.
Thomas BenfieldHvidovre Hospital, University of Copenhagen, Copenhagen, Denmark.
David MunroeSlidell, LA, USA.
Jens D LundgrenRigshospitalet, University of Copenhagen, Copenhagen, Denmark.
James D NeatonSchool of Public Health, University of Minnesota, Minneapolis, MN, USA.
INSIGHT START study group
University of Minnesota · USAgence Nationale de Recherches sur le Sida et les Hépatites Virales · FREvangelismos Hospital · GRGhent University Hospital · BEHospital Ramos Mejía · ARHvidovre Hospital · DKInstitute of Human Virology · NGLeicester Royal Infirmary · GBUniversidade Federal do Rio de Janeiro · BRUniversity College London · GBUniversity of Copenhagen · DKUniversity of the Witwatersrand · ZAUNSW Sydney · AUWashington University Medical Center · US

Funding

International Network for Strategic Initiatives in Global HIV Trials (INSIGHT)UM1AI068641 · NIAID · UNIVERSITY OF MINNESOTA · PI NEATON, JAMES DENNIS · 2011 to 2014
$83.5M
International Network for Strategic Initiatives in Global HIV Trials (INSIGHT): STARTUM1AI120197 · NIAID · UNIVERSITY OF MINNESOTA · PI NEATON, JAMES DENNIS · 2015 to 2017
$65.1M
Medical Research Council MC_UU_12023/23NIAID NIH HHS UM1 AI068641NIAID NIH HHS UM1 AI120197
6 · The paper itself

Abstract

backgroundImmediate initiation of antiretroviral therapy (ART) in asymptomatic adults with CD4 counts higher than 500 cells per μL, as recommended, might not always be possible in resource-limited settings. We aimed to identify subgroups of individuals who would benefit most from immediate treatment.

methodsThe START trial was a randomised controlled trial in asymptomatic, HIV-positive adults previously untreated with ART. Participants with CD4 counts higher than 500 cells per μL were randomly assigned to receive immediate ART or to defer ART until CD4 counts were lower than 350 cells per μL. The primary endpoint of the study was serious AIDS-defining illnesses or death from AIDS and serious non-AIDS illnesses or non-AIDS-related death. In this post-hoc analysis, we estimated event rates and absolute risk reduction with immediate versus deferred ART, overall and by subgroup. Subgroups were prespecified in the study protocol or formed post hoc on the basis of baseline characteristics associated with morbidity and mortality in people with HIV. For continuous characteristics, approximate terciles were chosen as subgroup cutoff points, unless different cutoffs were clinically meaningful (eg, age ≥50 years). We estimated the number needed to treat immediately with ART for 1 year to prevent one primary event. Heterogeneity in the absolute risk reduction between subgroups was assessed with bootstrap tests. The START trial is registered with ClinicalTrials.gov, number NCT00867048.

findingsBetween April 15, 2009, and Dec 23, 2013, we enrolled 4684 participants from 35 countries across five continents, of whom 2325 were assigned to immediate ART and 2359 were assigned to deferred ART. The primary endpoint occurred in 42 participants in the immediate ART group (0·58 events per 100 person-years) and 100 participants in the deferred ART group (1·37 events per 100 person-years). The absolute risk reduction was 0·80 (95% CI 0·48-1·13) per 100 person-years with immediate treatment, and the number needed to treat immediately to prevent one event was 126 (95% CI 89-208). Significant heterogeneity in absolute risk reduction with immediate ART was found across subgroups according to age (p=0·0022), CD4 to CD8 ratio (p=0·0007), and plasma HIV RNA viral load (p=0·033) at baseline. The highest absolute risk reductions and the lowest numbers needed to treat were found in participants aged 50 years or older, those with CD4 to CD8 ratios of less than 0·5, and those with plasma HIV RNA viral loads of 50 000 copies per mL or higher.

interpretationAsymptomatic, ART-naive adults with CD4 counts higher than 500 cells per μL who are older, have a low CD4 to CD8 ratio, or a high plasma HIV RNA viral load benefit most from immediate initiation of ART and should be prioritised for treatment.

fundingUS National Institute of Allergy and Infectious Diseases.

Indexed as

AdultAntiretroviral Therapy, Highly ActiveCD4 Lymphocyte CountFemaleHIV-1HIV InfectionsHumansMaleTreatment OutcomeViral LoadYoung Adult

Identifiers

PMID29352723
PMCPMC9287840
OpenAlexW2783440746

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

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.