Evidence map›Paper›PMID 30653541›Full record

ArticlePloS one2019

Real-life study of dual therapy based on dolutegravir and ritonavir-boosted darunavir in HIV-1-infected treatment-experienced patients.

Elżbieta Jabłonowska, Ewa Siwak, Monika Bociąga-Jasik, Jacek Gąsiorowski, Anna Kalinowska, Ewa Firląg Burkacka, Kamila Wójcik-Cichy, Anna Piątek, Iwona Cielniak, Andrzej Horban

Open access · goldAbstract readMulticenter Study
In one paragraph

Article in PloS one, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
1.7field-weighted citation impact, top 17% 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

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 19 citations in OpenAlex.

  1. A systematic review of the genetic mechanisms of dolutegravir resistance.The Journal of antimicrobial chemotherapy · 2019
    Pooled it
  2. Trial
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Simplifying ARV Therapy in the Setting of Resistance.Current infectious disease reports · 2019
    Review
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 4 institutions in 1 country.

Elżbieta JabłonowskaDepartment of Infectious Diseases and Hepatology, Medical University of Lodz, Lodz, Poland.ORCID 0000-0002-7282-1225
Ewa SiwakHospital for Infectious Diseases, HIV Out-Patient Clinic, Warsaw, Poland.
Monika Bociąga-JasikDepartment of Infectious Diseases, Jagiellonian University Medical College, Krakow, Poland.
Jacek GąsiorowskiDepartment of Infectious Diseases, Hepatology and Acquired Immune Deficiencies, Wroclaw Medical University, Wroclaw, Poland.
Anna KalinowskaDepartment of Infectious Diseases, Jagiellonian University Medical College, Krakow, Poland.
Ewa Firląg BurkackaHospital for Infectious Diseases, HIV Out-Patient Clinic, Warsaw, Poland.
Kamila Wójcik-CichyDepartment of Infectious Diseases and Hepatology, Medical University of Lodz, Lodz, Poland.
Anna PiątekDepartment of Infectious Diseases, Jagiellonian University Medical College, Krakow, Poland.
Iwona CielniakHospital for Infectious Diseases, HIV Out-Patient Clinic, Warsaw, Poland.
Andrzej HorbanHospital for Infectious Diseases, HIV Out-Patient Clinic, Warsaw, Poland.
Jagiellonian University · PLMedical University of Lodz · PLMedical University of Warsaw · PLWroclaw Medical University · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDual therapy based on dolutegravir and ritonavir-boosted darunavir (DTG/DRV/r) is a combination of well-known drugs with a high genetic barrier to HIV resistance.

methodA retrospective analysis of all HIV-1 infected treatment-experienced patients who switched to DTG/DRV/r from May 2014 till March 2017 in 4 Polish centres-results of a 48-week treatment.

resultsThe study group consisted of 59 men and 17 women. Median baseline parameters were: age- 42.7 years, CD4 cells count- 560.5 cells/μl, CD4 cells nadir- 150 cells/μl, number of prior antiretroviral regimens- 3. The introduction of dual therapy was primarily due to virologic failure (30 patients), adverse events on previous regimens (17 patients) and therapy simplification (27 patients). At week 48 the treatment was continued in 70/76 of patients and the median CD4 cells count increased from 560.5 to 641.0 cells/μl. The therapy was discontinued in six patients (1 -virologic failure, 1 -decrease of estimated glomerular filtration rate (eGFR), 1 -myalgia, 3 -lost to follow-up). At week 48 six patients had detectable viremia, but only in one patient viremia was higher than 200 copies/ml. At week 48 the level of serum total cholesterol of the investigated subjects was statistically significantly higher than at the moment of dual therapy introduction (185.8 mg/dl vs. 174.8 mg/dl- p<0.05). However, in patients previously not treated with TDF, there were no changes in lipid parameters during therapy. Proteinuria was observed in 13.2% of patients before the switch to dual therapy and in 7.1% of patients at week 48.

conclusionsThe investigated dual therapy was effective and safe. The observed increase in lipid parameters only concerned the patients who had used a TDF-based regimen prior to analysed dual treatment.

Indexed as

AdultAnti-HIV AgentsAntiretroviral Therapy, Highly ActiveCD4 Lymphocyte CountDarunavirDolutegravirDrug Therapy, CombinationFemaleHeterocyclic Compounds, 3-RingHIV-1HIV InfectionsHumansMaleMiddle AgedOutcome Assessment, Health CareOxazinesAnti-HIV AgentsDarunavirDolutegravirHeterocyclic Compounds, 3-RingOxazinesPiperazinesPyridonesRitonavir

Identifiers

PMID30653541
PMCPMC6336297
OpenAlexW2909009432

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.