Evidence map›Paper›PMID 33055569›Full record

ArticleAIDS (London, England)2020

Substantial decline in heavily treated therapy-experienced persons with HIV with limited antiretroviral treatment options.

Kristina L Bajema, Robin M Nance, Joseph A C Delaney, Ellen Eaton, Thibaut Davy-Mendez, Maile Y Karris, Richard D Moore, Joseph J Eron, Benigno Rodriguez, Kenneth H Mayer and 6 more

Open access · greenAbstract read
In one paragraph

Article in AIDS (London, England), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
0.4field-weighted citation impact, top 26% 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

19 citing papers in PubMed, 35 citations in OpenAlex.

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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

16 authors at 8 institutions in 1 country.

Kristina L BajemaDepartment of Medicine, Division of Allergy & Infectious Diseases, University of Washington, Seattle, Washington.
Robin M NanceDepartment of Medicine, Division of Allergy & Infectious Diseases, University of Washington, Seattle, Washington.
Joseph A C DelaneyDepartment of Medicine, Division of Allergy & Infectious Diseases, University of Washington, Seattle, Washington.
Ellen EatonDepartment of Medicine, Division of Infectious Diseases, University of Alabama Birmingham, Birmingham, Alabama.
Thibaut Davy-MendezDepartment of Epidemiology, University of North Carolina, Chapel Hill, North Carolina.
Maile Y KarrisDepartment of Medicine, Division of Infectious Diseases & Global Public Health, University of California, San Diego, California.
Richard D MooreDepartment of Medicine, Division of Infectious Diseases, Baltimore, Johns Hopkins University, Maryland, USA.
Joseph J EronDepartment of Epidemiology, University of North Carolina, Chapel Hill, North Carolina.
Benigno RodriguezDepartment of Medicine, Division of Infectious Diseases, Case Western Reserve University, Cleveland, Ohio.
Kenneth H MayerDepartment of Medicine, Division of Infectious Diseases, Fenway Health, Boston, Massachusetts.
Elvin GengDepartment of Medicine, Division of Infectious Diseases, University of California San Francisco, San Francisco, California.
Cindy GarrisViiV Healthcare, Research Triangle Park, North Carolina, USA.
Michael S SaagDepartment of Medicine, Division of Infectious Diseases, University of Alabama Birmingham, Birmingham, Alabama.
Heidi M CraneDepartment of Medicine, Division of Allergy & Infectious Diseases, University of Washington, Seattle, Washington.
Mari M KitahataDepartment of Medicine, Division of Allergy & Infectious Diseases, University of Washington, Seattle, Washington.
Centers for AIDS Research Clinical Network of Integrated Systems (CNICS)
University of Washington · USUniversity of Alabama at Birmingham · USUniversity of North Carolina at Chapel Hill · USCase Western Reserve University · USFenway Health · USJohns Hopkins Medicine · USUniversity of California, San Diego · USUniversity of California, San Francisco · US

Funding

University of Washington/Fred Hutch Center for AIDS ResearchP30AI027757 · NIAID · UNIVERSITY OF WASHINGTON · PI EDWIN ROBERTO ORELLANA · 1988 to 2026
$104.9M
Unsolicited R24 for the CFAR-Network of Integrated Clinical Sciences, CNICSR24AI067039 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Michael S. Saag · 2006 to 2026
$99.4M
The impact of HIV viral diversity and cellular immunity on HIV pathogenesisP30AI060354 · NIAID · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI RAJESH T GANDHI · 2004 to 2026
$94.4M
Virology CoreP30AI027763 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MALLORY O JOHNSON · 1988 to 2026
$93.6M
Virology CoreP30AI027767 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Latesha Ellen Elopre · 1988 to 2026
$84.1M
VirologyP30AI036214 · NIAID · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI David Mitchell Smith · 1994 to 2026
$78.4M
Virology, Immunology, and Microbiology CoreP30AI050410 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI DAVID M. MARGOLIS · 2001 to 2026
$76.9M
Vaccine Response and Immunotherapeutics SWGP30AI094189 · NIAID · JOHNS HOPKINS UNIVERSITY · PI Richard E. Chaisson · 2012 to 2026
$67.0M
WG3: HIV, Co-infections and Co-morbiditiesP30AI036219 · NIAID · CASE WESTERN RESERVE UNIVERSITY · PI Alan David Levine · 1994 to 2026
$50.0M
Johns Hopkins HIV Clinical CohortU01DA036935 · NIDA · JOHNS HOPKINS UNIVERSITY · PI MOORE, RICHARD DOUGLAS · 2014 to 2024
$14.9M
NIAID NIH HHS P30 AI027757NIAID NIH HHS P30 AI027763NIAID NIH HHS P30 AI027767NIAID NIH HHS P30 AI036214NIAID NIH HHS P30 AI036219NIAID NIH HHS P30 AI050410NIAID NIH HHS P30 AI060354NIAID NIH HHS P30 AI094189NIAID NIH HHS R24 AI067039NIDA NIH HHS U01 DA036935
6 · The paper itself

Abstract

objectiveHistorically, a high burden of resistance to antiretroviral therapy (ART) in heavily treatment-experienced (HTE) persons with HIV (PWH) resulted in limited treatment options (LTOs). We evaluated the prevalence, risk factors, and virologic control of HTE PWH with LTO throughout the modern ART era.

designWe examined all ART-experienced PWH in care between 2000 and 2017 in the Centers for AIDS Research Network of Integrated Clinical Systems cohort.

methodsWe computed the annual prevalence of HTE PWH with LTO defined as having two or less available classes with two or less active drugs per class based on genotypic data and cumulative antiretroviral resistance. We used multivariable Cox proportional hazards models to examine risk of LTO by 3-year study entry periods adjusting for demographic and clinical characteristics.

resultsAmong 27 133 ART-experienced PWH, 916 were classified as having LTO. The prevalence of PWH with LTO was 5.2-7.5% in 2000-2006, decreased to 1.8% in 2007, and remained less than 1% after 2012. Persons entering the study in 2009-2011 had an 80% lower risk of LTO compared with those entering in 2006-2008 (adjusted hazard ratio 0.20; 95% confidence interval: 0.09-0.42). We found a significant increase in undetectable HIV viral loads among PWH ever classified as having LTO from less than 30% in 2001 to more than 80% in 2011, comparable with persons who never had LTO.

conclusionResults of this large multicenter study show a dramatic decline in the prevalence of PWH with LTO to less than 1% with the availability of more potent drugs and a marked increase in virologic suppression in the current ART era.

Indexed as

AdultAnti-HIV AgentsAntiretroviral Therapy, Highly ActiveCohort StudiesDrug Resistance, ViralFemaleHIV-1HIV InfectionsHumansMaleMiddle AgedTreatment OutcomeViral LoadAnti-HIV Agents

Identifiers

PMID33055569
PMCPMC7606534
OpenAlexW3092824650

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Registered trials

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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.