Evidence map›Paper›PMID 28873128›Full record

Trial reportJAMA pediatrics2017

Safety and Feasibility of Antiretroviral Preexposure Prophylaxis for Adolescent Men Who Have Sex With Men Aged 15 to 17 Years in the United States.

Sybil G Hosek, Raphael J Landovitz, Bill Kapogiannis, George K Siberry, Bret Rudy, Brandy Rutledge, Nancy Liu, D Robert Harris, Kathleen Mulligan, Gregory Zimet and 8 more

Registry-linked trialOpen access · greenAbstract readClinical Trial, Phase IIMulticenter Study
In one paragraph

Trial report in JAMA pediatrics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01769456 (Project PrEPare - An Open Label Demonstration Project and Phase II Safety Study of Pre-Exposure Prophylaxis Use Among 15 to 17 Year Old Young Men Who Have Sex With Men), which is not on this map. Cited by 130 papers, 10 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
130citing papers in PubMed, 10 pooled it
16.8field-weighted citation impact, top 1% 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.

NCT01769456 phase2completednot on this map

Project PrEPare - An Open Label Demonstration Project and Phase II Safety Study of Pre-Exposure Prophylaxis Use Among 15 to 17 Year Old Young Men Who Have Sex With Men (YMSM) in the United States

TypeinterventionalSponsorUniversity of North Carolina, Chapel HillRan2013 to 2016Enrolled78ConditionsHIV InfectionArmsPCC, Emtricitabine/tenofovir (FTC/TDF (Truvada®))
3 · Its place in the literature

Who cites it

130 citing papers in PubMed, 10 syntheses or guidelines pooled it, 225 citations in OpenAlex.

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70 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

18 authors at 14 institutions in 1 country.

Sybil G HosekStroger Hospital of Cook County, Chicago, Illinois.
Raphael J LandovitzUniversity of California-Los Angeles, Los Angeles.
Bill KapogiannisNational Institute of Child Health and Human Development, Bethesda, Maryland.
George K SiberryNational Institute of Child Health and Human Development, Bethesda, Maryland.
Bret RudyNew York University, New York.
Brandy RutledgeWestat, Rockville, Maryland.
Nancy LiuWestat, Rockville, Maryland.
D Robert HarrisWestat, Rockville, Maryland.
Kathleen MulliganUniversity of California-San Francisco, San Francisco.
Gregory ZimetIndiana University, Indianapolis.
Kenneth H MayerFenway Institute, Boston, Massachusetts.
Peter AndersonUniversity of Colorado-Denver, Denver.
Jennifer J KiserUniversity of Colorado-Denver, Denver.
Michelle LallyBrown University, Providence, Rhode Island.
Jennifer BrothersStroger Hospital of Cook County, Chicago, Illinois.
Kelly BojanRuth Rothstein CORE Center, Chicago, Illinois.
Jim RooneyGilead Sciences, Foster City, California.
Craig M WilsonUniversity of Alabama-Birmingham, Birmingham.
Westat (United States) · USEunice Kennedy Shriver National Institute of Child Health and Human Development · USJohn H. Stroger, Jr. Hospital of Cook County · USBrown University · USFenway Health · USGilead Sciences (United States) · USIndiana University – Purdue University Indianapolis · USNew York University · USRuth M. Rothstein CORE Center · USUniversity of Alabama at Birmingham · USUniversity of California, Los Angeles · USUniversity of California, San Francisco · USUniversity of Colorado Denver · USUniversity of Denver · US

Funding

Adol. Medicine Trials Network for HIV/AIDS InterventionsU01HD040474 · NICHD · WESTAT, INC. · PI HARRIS, DONALD ROBERT · 2001 to 2016
$114.4M
LEADERSHIP GROUP FOR ADOLESCENT MEDICINE TRIALS NETWORKU01HD040533 · NICHD · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI WILSON, CRAIG M · 2001 to 2016
$76.4M
NICHD NIH HHS U01 HD040474NICHD NIH HHS U01 HD040533
6 · The paper itself

Abstract

Importance: Adolescents represent a key population for implementing preexposure prophylaxis (PrEP) interventions worldwide, yet tenofovir disoproxil fumarate/emtricitabine (TDF/FTC) for PrEP is only licensed for adults. Objective: To examine the safety of and adherence to PrEP along with changes in sexual risk behavior among adolescent men who have sex with men (MSM). Design, Setting, and Participants: Adolescent Medicine Trials Network for HIV/AIDS Interventions 113 (Project PrEPare) was a PrEP demonstration project that evaluated the safety, tolerability, and acceptability of TDF/FTC and patterns of use, rates of adherence, and patterns of sexual risk behavior among healthy young MSM aged 15 to 17 years. Participants were recruited from adolescent medicine clinics and their community partners in 6 US cities, had negative test results for human immunodeficiency virus (HIV) but were at high risk for acquiring an infection, and were willing to participate in a behavioral intervention and accept TDF/FTC as PrEP. Exposures: All participants completed an individualized evidence-based behavioral intervention and were provided with daily TDF/FTC as PrEP for 48 weeks. Main Outcomes and Measures: The main objectives were to: (1) provide additional safety data regarding TDF/FTC use among young MSM who had negative test results for HIV; (2) examine the acceptability, patterns of use, rates of adherence, and measured levels of tenofovir diphosphate in dried blood spots; and (3) examine patterns of risk behavior when young MSM were provided with a behavioral intervention in conjunction with open-label TDF/FTC. Results: Among 2864 individuals screened (from August 2013 to September 2014), 260 were eligible and 78 were enrolled (mean [SD] age, 16.5 [0.73] years), of whom 2 (3%) were Asian/Pacific Islander, 23 (29%) were black/African American, 11 (14%) were white, 16 (21%) were white Hispanic, and 26 (33%) were other/mixed race/ethnicity. Over 48 weeks of PrEP use, 23 sexually transmitted infections were diagnosed in 12 participants. The HIV seroconversion rate was 6.4 (95% CI: 1.3-18.7) per 100 person-years. Tenofovir diphosphate levels consistent with a high degree of anti-HIV protection (>700 fmol/punch) were found in 42 (54%), 37 (47%), 38 (49%), 22 (28%), 13 (17%), and 17 (22%) participants at weeks 4, 8, 12, 24, 36, and 48, respectively. Conclusions and Relevance: Adolescent Medicine Trials Network for HIV/AIDS Interventions 113 enrolled a diverse sample of adolescent MSM at risk for HIV who consented to study participation. Approximately half achieved protective drug levels during the monthly visits, but adherence decreased with quarterly visits. Youth may need additional contact with clinical staff members to maintain high adherence. Trial Registration: clinicaltrials.gov Identifier: NCT01769456.

Indexed as

Homosexuality, MalePre-Exposure ProphylaxisAdolescentAnti-HIV AgentsDrug MonitoringEmtricitabine, Tenofovir Disoproxil Fumarate Drug CombinationFeasibility StudiesFollow-Up StudiesHIV InfectionsHumansMaleRisk-TakingTreatment OutcomeUnited StatesAnti-HIV AgentsEmtricitabine, Tenofovir Disoproxil Fumarate Drug Combination

Identifiers

PMID28873128
PMCPMC5710370
OpenAlexW2753665408

What OpenQuestion holds

Textmetadata
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.