Evidence map›Paper›PMID 26605505›Full record

Trial reportJournal of acquired immune deficiency syndromes (1999)2016

Brief Report: Switch to Ritonavir-Boosted Atazanavir Plus Raltegravir in Virologically Suppressed Patients With HIV-1 Infection: A Randomized Pilot Study.

Jan van Lunzen, Anton Pozniak, Jose M Gatell, Andrea Antinori, Isabelle Klauck, Oscar Serrano, Adyb Baakili, Olayemi Osiyemi, Heather Sevinsky, Pierre-Marie Girard

Open access · greenAbstract readMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Journal of acquired immune deficiency syndromes (1999), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
2.7field-weighted citation impact, top 10% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 23 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Review
  4. Article
  5. Review
  6. Barrier to Resistance of Dolutegravir in Two-Drug Combinations.Antimicrobial agents and chemotherapy · 2019
    Article
  7. Observational
  8. Review
  9. Review
  10. Observational
  11. Article
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

10 authors at 1 institution in 2 countries.

Jan van Lunzen*Infectious Diseases Unit, University Medical Center Hamburg-Eppendorf, Hamburg, Germany; †ViiV Healthcare, Brentford, United Kingdom; ‡Chelsea and Westminster NHS Foundation Trust Hospital, London, United Kingdom; §Infectious Diseases & AIDS Units, Clinical Institute of Medicine & Dermatology, Hospital Clinic, University of Barcelona, Barcelona, Spain; ‖National Institute for Infectious Diseases Lazzaro Spallanzani IRCCS, Roma, Italy; ¶Bristol-Myers Squibb, Rueil-Malmaison, France; #Bristol-Myers Squibb, Madrid, Spain; **Bristol-Myers Squibb, Uxbridge, United Kingdom; ††Triple O Research Institute PA, West Palm Beach, FL; ‡‡Bristol-Myers Squibb, Princeton, NJ; §§Department of Infectious and Tropical Diseases, Hôpital St Antoine, Assistance Publique-Hôpitaux de Paris, Paris, France; and ‖‖Institut Pierre-Louis d'Epidémiologie et Santé Publique, Institut National de la Santé et de la Recherche Médicale, Unité Mixte de Recherche en Santé n°1136, Paris, France.
Anton Pozniak
Jose M Gatell
Andrea Antinori
Isabelle Klauck
Oscar Serrano
Adyb Baakili
Olayemi Osiyemi
Heather Sevinsky
Pierre-Marie Girard
Universität Hamburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This open-label, multinational, pilot study randomized (1:2 ratio) adults with HIV-1 RNA <40 copies per milliliter and nucleos(t)ide-related safety/tolerability issues to switch to ritonavir-boosted atazanavir (ATV/r) plus tenofovir disoproxil fumarate/emtricitabine (n = 37) or the nucleos(t)ide reverse transcriptase inhibitor-sparing regimen of ATV/r plus raltegravir (RAL) (n = 72). At 24 weeks, 35/37 (94.6%) and 58/72 (80.6%) of patients, respectively, maintained virological suppression, the primary endpoint, and 1 (2.7%) and 7 (9.7%), respectively, experienced virological rebound. Corresponding 48-week proportions were 86.5%, 69.4%, 2.7%, and 12.5%, respectively. Adherence was lower and treatment discontinuation was higher with ATV/r+RAL. In conclusion, switching to ATV/r+RAL resulted in a higher virological rebound rate than switching to ATV/r plus tenofovir disoproxil fumarate/emtricitabine.

Indexed as

Drug SubstitutionHIV-1AdultAtazanavir SulfateDrug Therapy, CombinationFemaleHIV InfectionsHIV Integrase InhibitorsHIV Protease InhibitorsHumansMaleMiddle AgedPilot ProjectsProspective StudiesRaltegravir PotassiumReverse Transcriptase InhibitorsAtazanavir SulfateHIV Integrase InhibitorsHIV Protease InhibitorsRaltegravir PotassiumReverse Transcriptase InhibitorsRitonavir

Identifiers

PMID26605505
PMCPMC4804741
OpenAlexW2316844105

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.