Evidence map›Paper›PMID 31463794›Full record

ArticlePaediatric drugs2019

Canakinumab in Children with Familial Mediterranean Fever: A Single-Center, Retrospective Analysis.

Rabia Miray Kisla Ekinci, Sibel Balci, Dilek Dogruel, Derya Ufuk Altintas, Mustafa Yilmaz

Abstract read
PubMed Publisher
In one paragraph

Article in Paediatric drugs, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
1.1field-weighted citation impact, top 22% 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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 22 citations in OpenAlex.

  1. Pooled it
  2. Systematic Review of Adverse Events of IL-1 and IL-6 Inhibitor Use in Pediatrics.The journal of pediatric pharmacology and therapeutics : JPPT : the official journal of PPAG · 2025
    Article
  3. Familial Mediterranean Fever in Childhood.Turkish archives of pediatrics · 2024
    Review
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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

5 authors at 1 institution in 1 country.

Rabia Miray Kisla EkinciDepartment of Pediatric Rheumatology, Cukurova University Faculty of Medicine, Adana, 01331, Turkey. mir_kisla@hotmail.com.ORCID http://orcid.org/0000-0001-6234-822X
Sibel BalciDepartment of Pediatric Rheumatology, Cukurova University Faculty of Medicine, Adana, 01331, Turkey.ORCID http://orcid.org/0000-0003-0099-313X
Dilek DogruelDepartment of Pediatric Allergy and Immunology, Cukurova University Faculty of Medicine, Adana, Turkey.ORCID http://orcid.org/0000-0003-3972-7277
Derya Ufuk AltintasDepartment of Pediatric Allergy and Immunology, Cukurova University Faculty of Medicine, Adana, Turkey.ORCID http://orcid.org/0000-0003-2090-5248
Mustafa YilmazDepartment of Pediatric Rheumatology, Cukurova University Faculty of Medicine, Adana, 01331, Turkey.ORCID http://orcid.org/0000-0002-6213-8289
Cukurova University · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionFamilial Mediterranean fever (FMF) is an autoinflammatory disease characterized by interleukin (IL)-1 overproduction. Colchicine is the mainstay drug in the treatment of FMF; however, a minority of patients do not respond despite the highest tolerated doses. We aimed to share our experience with canakinumab, a human monoclonal antibody against IL-1β, in pediatric FMF patients.

methodsThis historical, single-cohort study retrospectively evaluated the disease characteristics, indications, and treatment responses of 14 pediatric FMF patients treated with canakinumab in our pediatric rheumatology department.

resultsThe median age at onset and diagnosis of 14 FMF patients (9 females, 5 males), were 3.5 (range 0.5-10) years and 6 (range 3-16) years, respectively. Indications for canakinumab treatment were renal amyloidosis (n = 1), colchicine resistance (n = 11), and persistent arthritis (n = 2). Only two (14.3%) patients had colchicine intolerance. Complete response was obtained in 10/14 (71.5%) among all patients and 10/12 (86%) in patients with typical phenotype. The patient with chronic oligoarthritis had a complete response, whereas the patient with rheumatoid factor (RF)-positive polyarthritis demonstrated an initial partial response to canakinumab treatment. We found that attack frequency, proteinuria, and acute phase reactants, including erythrocyte sedimentation rate and C-reactive protein, were significantly decreased after canakinumab treatment in children with FMF.

conclusionCanakinumab may be an effective treatment option for pediatric FMF patients with colchicine resistance, renal amyloidosis, and chronic oligoarthritis. Further studies are needed to clarify the efficacy of canakinumab in patients with a second disease, RF-positive polyarticular juvenile idiopathic arthritis.

Indexed as

AdolescentAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedChildChild, PreschoolCohort StudiesFamilial Mediterranean FeverFemaleHumansInfantInfant, NewbornInterleukin-1betaMaleRetrospective StudiesTreatment OutcomeAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedcanakinumabInterleukin-1beta

Identifiers

PMID31463794
OpenAlexW2970871122

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.