Evidence map›Paper›PMID 31769856›Full record

ReviewRheumatology (Oxford, England)2019

Anakinra in children and adults with Still's disease.

Sebastiaan J Vastert, Yvan Jamilloux, Pierre Quartier, Sven Ohlman, Lisa Osterling Koskinen, Torbjörn Kullenberg, Karin Franck-Larsson, Bruno Fautrel, Fabrizio de Benedetti

Abstract readReview
In one paragraph

Review in Rheumatology (Oxford, England), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed, 2 pooled it
–field-weighted citation impact
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

53 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
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  8. NF-κB in inflammation and cancer.Cellular & molecular immunology · 2025
    Review
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  10. His brain is on FIRES.Journal of neurology · 2024
    Article
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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

9 authors.

Sebastiaan J VastertDepartment of Pediatric Rheumatology and Laboratory of Translational Immunology, University Medical Centre Utrecht, Utrecht, The Netherlands.
Yvan JamillouxDepartment of Internal Medicine Hospices Civils de Lyon, Croix-Rousse Hospital, Lyon, France.
Pierre QuartierPediatric Immunology-Hematology and Rheumatology Unit, RAISE Rare Disease Reference Centre, IMAGINE Institute, Necker Hospital, Assistance Publique Hôpitaux de Paris, Paris, France.
Sven OhlmanSobi, Stockholm, Sweden.
Lisa Osterling KoskinenSobi, Stockholm, Sweden.
Torbjörn KullenbergSobi, Stockholm, Sweden.
Karin Franck-LarssonSobi, Stockholm, Sweden.
Bruno FautrelDepartment of Rheumatology, AP-HP Pitié-Salpêtrière Hospital, Paris, France.
Fabrizio de BenedettiDivision of Rheumatology, Ospedale Pediatrico Bambino Gesù, Rome, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Systemic juvenile idiopathic arthritis and adult-onset Still's disease are rare autoinflammatory disorders with common features, supporting the recognition of these being one disease-Still's disease-with different ages of onset. Anakinra was recently approved by the European Medicines Agency for Still's disease. In this review we discuss the reasoning for considering Still's disease as one disease and present anakinra efficacy and safety based on the available literature. The analysis of 27 studies showed that response to anakinra in Still's disease was remarkable, with clinically inactive disease or the equivalent reported for 23-100% of patients. Glucocorticoid reduction and/or stoppage was reported universally across the studies. In studies on paediatric patients where anakinra was used early or as first-line treatment, clinically inactive disease and successful anakinra tapering/stopping occurred in >50% of patients. Overall, current data support targeted therapy with anakinra in Still's disease since it improves clinical outcome, especially if initiated early in the disease course.

Indexed as

AdultAntirheumatic AgentsArthritis, JuvenileChildDose-Response Relationship, DrugDrug Administration ScheduleDrug ApprovalFemaleHumansInterleukin 1 Receptor Antagonist ProteinMalePatient SafetySeverity of Illness IndexStill's Disease, Adult-OnsetTreatment OutcomeAntirheumatic AgentsInterleukin 1 Receptor Antagonist Proteinadult-onset Still’s disease (AOSD)anakinraIL-1IL-1 receptor antagonist (IL-1Ra)Still’s diseasesystemic juvenile idiopathic arthritis (sJIA)

Identifiers

PMID31769856
PMCPMC6878842

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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.