Evidence map›Paper›PMID 26374404›Full record

ArticleAnnals of the rheumatic diseases2016

Effectiveness of tocilizumab with and without synthetic disease-modifying antirheumatic drugs in rheumatoid arthritis: results from a European collaborative study.

Cem Gabay, Myriam Riek, Merete Lund Hetland, Ellen-Margrethe Hauge, Karel Pavelka, Matija Tomšič, Helena Canhao, Katerina Chatzidionysiou, Galina Lukina, Dan C Nordström and 6 more

Open access · hybridAbstract read
In one paragraph

Article in Annals of the rheumatic diseases, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
9.4field-weighted citation impact, top 2% 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

35 citing papers in PubMed, 70 citations in OpenAlex.

  1. Trial
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  8. Pathogenic mechanisms of cardiovascular damage in COVID-19.Molecular medicine (Cambridge, Mass.) · 2024
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  11. Cardiovascular Implications of Immune Disorders in Women.Circulation research · 2022 · on this map
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  12. Article
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  14. Antibody-Based Therapeutics for Atherosclerosis and Cardiovascular Diseases.International journal of molecular sciences · 2021
    Review
  15. Article
  16. Article
  17. Observational
  18. Article
  19. Anticytokine Immune Therapy and Atherothrombotic Cardiovascular Risk.Arteriosclerosis, thrombosis, and vascular biology · 2019
    Review
  20. 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

16 authors at 14 institutions in 11 countries.

Cem GabayDivision of Rheumatology, University Hospitals of Geneva, Geneva, Switzerland.
Myriam RiekSCQM Foundation, Zurich, Switzerland.
Merete Lund HetlandDANBIO, Center for Rheumatology and Spine Diseases, Rigshospitalet, Glostrup, Denmark Department of Clinical Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Glostrup, Denmark.
Ellen-Margrethe HaugeDepartment of Rheumatology, Aarhus University Hospital, Aarhus, Denmark.
Karel PavelkaInstitute of Rheumatology and Clinic of Rheumatology, Charles University Prague, Prague, Czech Republic.
Matija TomšičUniversity Medical Center, Ljubljana, Slovenia.
Helena CanhaoRheumatology Research Unit, Instituto de Medicina Molecular, Lisbon, Portugal, on behalf of the Rheumatic Diseases Portuguese Register (Reuma.pt).
Katerina ChatzidionysiouThe Karolinska Institute, Stockholm, Sweden.
Galina LukinaInstitute of Rheumatology, Moscow, Russia.
Dan C NordströmDepartment of Medicine, Helsinki University Central Hospital and University of Helsinki, Helsinki, Finland.
Elisabeth LieDepartment of Rheumatology, Diakonhjemmet Hospital, Oslo, Norway.
Ioan AncutaCantacuzino Hosp, Bucharest, Romania.
M Victoria HernándezRheumatology Department, Hospital Clinic of Barcelona, Barcelona, Spain.
Piet L M C van RielRadboud University Nijmegen Medical Centre, Nijmegen, the Netherlands.
Ronald van VollenhovenThe Karolinska Institute, Stockholm, Sweden.
Tore K KvienDepartment of Rheumatology, Diakonhjemmet Hospital, Oslo, Norway.
Diakonhjemmet Hospital · NOKarolinska Institutet · SEAarhus University Hospital · DKGlostrup Hospital · DKHospital Clínic de Barcelona · ESInstitute of Rheumatology · CZInstituto de Medicina Molecular João Lobo AntunesInstitutul Cantacuzino · ROLjubljana University Medical Centre · SIRadboud University Nijmegen · NLSCQM Foundation · CHUniversity Hospital of Geneva · CHUniversity of Helsinki · FIVA Nasonova Scientific Research Institute of Rheumatology · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesTo examine the effectiveness of tocilizumab (TCZ) with and without synthetic disease-modifying antirheumatic drugs (sDMARDs) in a large observational study.

methodsPatients with rheumatoid arthritis treated with TCZ who had a baseline visit and information on concomitant sDMARDs were included. According to baseline data, patients were considered as taking TCZ as monotherapy or combination with sDMARDs. Main study outcomes were the change of Clinical Disease Activity Index (CDAI) and TCZ retention. The prescription of TCZ as monotherapy was analysed using logistic regression. CDAI change was analysed with a mixed-effects model for longitudinal data. TCZ retention was analysed with a stratified extended Cox model.

resultsMultiple-adjusted analysis suggests that prescription of TCZ as monotherapy varied according to age, corticosteroid use, country of the registry and year of treatment initiation. The change of disease activity assessed by CDAI as well as the likelihood to be in remission were not significantly different whether TCZ was used as monotherapy or in combination with sDMARDs in a covariate-adjusted analysis. Estimates for unadjusted median TCZ retention were 2.3 years (95% CI 1.8 to 2.7) for monotherapy and 3.7 years (lower 95% CI limit 3.1, upper limit not estimable) for combination therapies. In a covariate-adjusted analysis, TCZ retention was also reduced when used as monotherapy, with an increasing difference between mono and combination therapy over time after 1.5 years (p=0.002).

conclusionsTCZ with or without concomitant sDMARDs resulted in comparable clinical response as assessed by CDAI change, but TCZ retention was shorter under monotherapy of TCZ.

Indexed as

Antibodies, Monoclonal, HumanizedAntirheumatic AgentsArthritis, RheumatoidDrug Therapy, CombinationEuropeFemaleHumansMaleMiddle AgedSeverity of Illness IndexTreatment OutcomeAntibodies, Monoclonal, HumanizedAntirheumatic AgentstocilizumabDMARDs (biologic)DMARDs (synthetic)Rheumatoid ArthritisTreatment

Identifiers

PMID26374404
PMCPMC4941183
OpenAlexW2227181458

What OpenQuestion holds

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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.