Evidence map›Paper›PMID 25397616›Full record

ArticlePloS one2014

HIV cure strategies: how good must they be to improve on current antiretroviral therapy?

Paul E Sax, Alexis Sypek, Bethany K Berkowitz, Bethany L Morris, Elena Losina, A David Paltiel, Kathleen A Kelly, George R Seage, Rochelle P Walensky, Milton C Weinstein and 2 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

14 citing papers in PubMed, 19 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 6 institutions in 1 country.

Paul E SaxDivision of Infectious Diseases, Brigham and Women's Hospital, Boston, Massachusetts, United States of America; Harvard University Center for AIDS Research, Harvard University, Boston, Massachusetts, United States of America.
Alexis SypekDivision of General Medicine, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts, United States of America; Medical Practice Evaluation Center, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts, United States of America.
Bethany K BerkowitzDivision of General Medicine, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts, United States of America; Medical Practice Evaluation Center, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts, United States of America.
Bethany L MorrisDivision of General Medicine, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts, United States of America; Medical Practice Evaluation Center, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts, United States of America.
Elena LosinaDepartment of Orthopedic Surgery, Brigham and Women's Hospital, Boston, Massachusetts, United States of America; Harvard University Center for AIDS Research, Harvard University, Boston, Massachusetts, United States of America; Division of General Medicine, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts, United States of America; Medical Practice Evaluation Center, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts, United States of America; Department of Biostatistics, Boston University School of Public Health, Boston, Massachusetts, United States of America.
A David PaltielYale School of Public Health, New Haven, Connecticut, United States of America.
Kathleen A KellyDivision of General Medicine, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts, United States of America; Medical Practice Evaluation Center, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts, United States of America.
George R SeageHarvard School of Public Health, Harvard University, Boston, Massachusetts, United States of America.
Rochelle P WalenskyDivision of Infectious Diseases, Brigham and Women's Hospital, Boston, Massachusetts, United States of America; Harvard University Center for AIDS Research, Harvard University, Boston, Massachusetts, United States of America; Division of Infectious Diseases, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts, United States of America; Medical Practice Evaluation Center, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts, United States of America.
Milton C WeinsteinHarvard School of Public Health, Harvard University, Boston, Massachusetts, United States of America.
Joseph EronDivision of Infectious Disease, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, United States of America.
Kenneth A FreedbergHarvard University Center for AIDS Research, Harvard University, Boston, Massachusetts, United States of America; Harvard School of Public Health, Harvard University, Boston, Massachusetts, United States of America; Division of General Medicine, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts, United States of America; Division of Infectious Diseases, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts, United States of America; Medical Practice Evaluation Center, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts, United States of America; Department of Epidemiology, Boston University School of Public Health, Boston, Massachusetts, United States of America.
Massachusetts General Hospital · USHarvard University · USBoston University · USBrigham and Women's Hospital · USJohns Hopkins University Center for AIDS ResearchUniversity of North Carolina at Chapel Hill · US

Funding

AIDS Clinical Trials Group NetworkU01AI068636 · NIAID · SOCIAL AND SCIENTIFIC SYSTEMS, INC. · PI KURITZKES, DANIEL R. · 2006 to 2010
$147.1M
Virology, Immunology, and Microbiology CoreP30AI050410 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI DAVID M. MARGOLIS · 2001 to 2026
$76.9M
University of North Carolina Global HIV Prevention and Treatment Clinical Trials Unit 2024 SupplementUM1AI069423 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Joseph J Eron, MINA CHRISTINE HOSSEINIPOUR · 2012 to 2026
$71.8M
Partners Healthcare Systems/Harvard Medical School/Boston Medical Center AIDS CTUU01AI069472 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI KURITZKES, DANIEL R. · 2007 to 2011
$15.4M
Cost-effectiveness of preventing HIV complicationsR37AI042006 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI FREEDBERG, KENNETH ALAN · 2006 to 2014
$7.1M
Novel Methods to Inform HIV/TB Clinical Trial DevelopmentR01AI093269 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI REDDY, KRISHNA P · 2011 to 2024
$6.8M
Antiretroviral Therapy for HIV-Infected PatientsK24AI051966 · NIAID · WEILL MEDICAL COLL OF CORNELL UNIV · PI GULICK, ROY M. · 2003 to 2012
$1.6M
HIV cure studies: risk, risk perception, and ethicsR56AI114617 · NIAID · HARVARD MEDICAL SCHOOL · PI EYAL, NIR · 2014 to 2014
$528k
NIAID NIH HHS AI051966NIAID NIH HHS K24 AI051966NIAID NIH HHS P30 AI050410NIAID NIH HHS R01 AI093269NIAID NIH HHS R37 AI042006NIAID NIH HHS R56 AI114617NIAID NIH HHS U01 AI068636NIAID NIH HHS U01 AI 069472NIAID NIH HHS U01 AI069472NIAID NIH HHS UM1 AI 069423NIAID NIH HHS UM1 AI069423
6 · The paper itself

Abstract

backgroundWe examined efficacy, toxicity, relapse, cost, and quality-of-life thresholds of hypothetical HIV cure interventions that would make them cost-effective compared to life-long antiretroviral therapy (ART).

methodsWe used a computer simulation model to assess three HIV cure strategies: Gene Therapy, Chemotherapy, and Stem Cell Transplantation (SCT), each compared to ART. Efficacy and cost parameters were varied widely in sensitivity analysis. Outcomes included quality-adjusted life expectancy, lifetime cost, and cost-effectiveness in dollars/quality-adjusted life year ($/QALY) gained. Strategies were deemed cost-effective with incremental cost-effectiveness ratios <$100,000/QALY.

resultsFor patients on ART, discounted quality-adjusted life expectancy was 16.4 years and lifetime costs were $591,400. Gene Therapy was cost-effective with efficacy of 10%, relapse rate 0.5%/month, and cost $54,000. Chemotherapy was cost-effective with efficacy of 88%, relapse rate 0.5%/month, and cost $12,400/month for 24 months. At $150,000/procedure, SCT was cost-effective with efficacy of 79% and relapse rate 0.5%/month. Moderate efficacy increases and cost reductions made Gene Therapy cost-saving, but substantial efficacy/cost changes were needed to make Chemotherapy or SCT cost-saving.

conclusionsDepending on efficacy, relapse rate, and cost, cure strategies could be cost-effective compared to current ART and potentially cost-saving. These results may help provide performance targets for developing cure strategies for HIV.

Indexed as

AdultAnti-HIV AgentsCohort StudiesComputer SimulationCost-Benefit AnalysisFemaleGenetic TherapyHIV InfectionsHumansLife ExpectancyMaleMiddle AgedQuality-Adjusted Life YearsRecurrenceStem Cell TransplantationAnti-HIV Agents

Identifiers

PMID25397616
PMCPMC4232561
OpenAlexW2119145497

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.