Evidence map›Paper›PMID 41933457›Full record

ArticleACR open rheumatology2026

Effectiveness of Canakinumab for First-Line Steroid-Free Treatment in Systemic-Onset Juvenile Idiopathic Arthritis and Juvenile Still Disease.

Gerd Horneff, Tilman Kallinich, Markus Hufnagel, Kirsten Minden, Frank Weller-Heinemann, Ralf Trauzeddel, Dirk Foell, Claas Hinze, Fabienne Staubi, Ariane Klein

Abstract read
In one paragraph

Article in ACR open rheumatology, 2026. 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. 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.

Gerd HorneffDepartment of General Paediatrics, Asklepios Clinic Sankt Augustin, Sankt Augustin, Germany.ORCID https://orcid.org/0000-0001-5491-7832
Tilman KallinichDepartment of Rheumatology and Clinical Immunology, German Rheumatism Research Centre Berlin and Charité University Medicine, Berlin, Germany.
Markus HufnagelDivision of Pediatric Rheumatology and Clinical Infectious Diseases, Department of General Pediatrics, Adolescent Medicine and Neonatology, Center for Pediatrics, Medical Center and Medical Faculty, University of Freiburg, Freiburg, Germany.
Kirsten MindenDepartment of Rheumatology and Clinical Immunology, German Rheumatism Research Centre Berlin and Charité University Medicine, Berlin, Germany.ORCID https://orcid.org/0000-0003-2775-0111
Frank Weller-HeinemannKlinikum Bremen-Mitte, Eltern-Kind-Zentrum Prof. Hess, Bremen, Germany.
Ralf TrauzeddelKlinik für Kinder und Jugendmedizin, Berlin, Germany.
Dirk FoellKlinik für Pädiatrische Rheumatologie und Immunologie, Universitätsklinik Münster, Münster, Germany.
Claas HinzeKlinik für Pädiatrische Rheumatologie und Immunologie, Universitätsklinik Münster, Münster, Germany.ORCID https://orcid.org/0000-0001-9247-4729
Fabienne StaubiDepartment of General Paediatrics, Asklepios Clinic Sankt Augustin, Sankt Augustin, Germany.
Ariane KleinDepartment of General Paediatrics, Asklepios Clinic Sankt Augustin, Sankt Augustin, Germany.ORCID https://orcid.org/0000-0001-9771-8710

Funding

Kinderrheumazentrum Sankt Augustin gGmbHNovartis Pharma GmbH
6 · The paper itself

Abstract

objectiveThis prospective study assesses the response to canakinumab monotherapy administered as three monthly subcutaneous injections in glucocorticoid-naïve patients with newly diagnosed systemic juvenile idiopathic arthritis (sJIA) and Still disease and evaluates the durability of drug-free inactive disease for up to nine months after canakinumab cessation.

methodsIn a multicenter, two-phase open-label study of newly diagnosed sJIA or Still disease, canakinumab was administered at 4 mg/kg subcutaneously every 4 weeks for 12 weeks. Thereafter, patients were followed for an additional 40 weeks. Routine care was provided to nonresponders.

resultsIn total, 21 patients were recruited, and 1 was excluded due to protocol violations. Fever resolved immediately in 17/19 patients. Two nonresponders (n = 2) were managed with different strategies: one received steroids alone, and the other received steroids plus canakinumab as part of routine care. By week 12, 14 patients achieved inactive disease. Thereafter, two flares occurred at weeks 24 and 36. Macrophage activation syndrome (MAS) was diagnosed in a third patient at week 19 and responded to treatment with glucocorticoids and cyclosporine A. By week 52, 11 patients had reached drug-free inactive disease and 3 had minimal disease activity. A total of 97 adverse events were reported; four were serious (one MAS, two disease flares, and one viral infection), but none were attributed to the study drug.

conclusionCanakinumab steroid-free first-line therapy in newly diagnosed sJIA induces long-lasting, drug-free inactive disease in a substantial proportion of patients. Discontinuation of canakinumab was associated with disease flares in a minority of patients.

Identifiers

PMID41933457
PMCPMC13052215

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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.