Evidence map›Paper›PMID 41121260›Full record

ArticlePediatric rheumatology online journal2025

Long-term safety of canakinumab in patients with systemic juvenile idiopathic arthritis: 5-year results from the Childhood Arthritis and Rheumatology Research Alliance (CARRA) registry.

Colleen Correll, Alis Burciu, Amita Bansal, Anne Dennos, Deepak Narayanswamy, Elodie Aubrun, Laura E Schanberg, Li Yuhan, Rahel Schneider, Stephen Balevic and 3 more

Abstract read
In one paragraph

Article in Pediatric rheumatology online journal, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–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

1 citing paper in PubMed.

  1. 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

13 authors.

Colleen CorrellDepartment of Pediatrics, University of Minnesota, Minneapolis, MN, USA.
Alis BurciuNovartis Pharma AG, Basel, Switzerland.
Amita BansalNovartis Pharma AG, Basel, Switzerland.
Anne DennosDuke Clinical Research Institute, Duke University School of Medicine, Durham, NC, USA.
Deepak NarayanswamyNovartis Healthcare Pvt Ltd, Hyderabad, India.
Elodie AubrunNovartis Pharma AG, Basel, Switzerland.
Laura E SchanbergDepartment of Pediatrics, Duke Clinical Research Institute, Duke University School of Medicine, Durham, NC, USA.
Li YuhanNovartis Pharmaceuticals Corporation, East Hanover, NJ, USA.
Rahel SchneiderNovartis Pharma AG, Basel, Switzerland.
Stephen BalevicDepartment of Pediatrics, Duke Clinical Research Institute, Duke University School of Medicine, Durham, NC, USA.
Yukiko KimuraJoseph M. Sanzari Children's Hospital, Hackensack Meridian School of Medicine, Nutley, NJ, USA.
Timothy BeukelmanChildhood Arthritis and Rheumatology Research Alliance, Washington D.C, USA. tbeukelman@carragroup.org.
CARRA Registry investigators

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSystemic juvenile idiopathic arthritis (SJIA) is a severe form of juvenile idiopathic arthritis characterized by fever, rash, chronic arthritis, and systemic inflammation. The introduction of biologics has improved the treatment options for SJIA. Canakinumab selectively inhibits interleukin-1β and is approved for SJIA treatment. In this study that utilized the Childhood Arthritis and Rheumatology Research Alliance (CARRA) Registry, long-term safety data available from patients with SJIA who started either canakinumab treatment or an alternative therapy were assessed.

methodsThis long-term, prospective, non-interventional study was conducted from August 2015 to June 2022 using data from the CARRA Registry. Data for serious adverse events (SAEs) and pre-specified events of special interest (ESIs) were collected from patients with SJIA aged between ≥ 2 and < 18 years at the time of treatment initiation and followed for a minimum of 5 years. Data were summarized descriptively, and no hypothesis testing was performed.

resultsThe final analysis included 177 patients: 90 in the overall canakinumab group (incident users [N = 39] and prevalent users [N = 51]) and 87 in the alternative treatment group. Median patient age at treatment initiation was 8.0 years in the overall canakinumab group. The incidence rates of SAEs per 100 patient-years were 3.62 (overall canakinumab group) and 3.39 (canakinumab incident users group). Of the predefined ESIs, macrophage activation syndrome (n = 5) and infections treated with intravenous anti-infectives (n = 1) were observed in the overall canakinumab group. The majority of patients (72.2%) treated with canakinumab received on-label dosing at some point during the first 5 years of the study.

conclusionsOverall, no changes were observed in the safety profile with long-term use of canakinumab in pediatric patients with SJIA. Particularly, no change in the frequency or severity of known ESIs occurred, and no new risks were identified. The findings suggest that canakinumab is effective in SJIA management and has a favorable safety profile with long-term use over a period of 5 years in real-world settings.

Indexed as

Antibodies, Monoclonal, HumanizedAntirheumatic AgentsArthritis, JuvenileAdolescentChildChild, PreschoolFemaleHumansInterleukin-1betaMaleProspective StudiesRegistriesTreatment OutcomeAntibodies, Monoclonal, HumanizedAntirheumatic AgentscanakinumabInterleukin-1betaCanakinumabCARRA registrySafetySystemic juvenile idiopathic arthritis

Identifiers

PMID41121260
PMCPMC12538899

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.