Evidence map›Paper›PMID 40977426›Full record

ArticleArthritis & rheumatology (Hoboken, N.J.)2026

Effect of Time to Start of Biologic Therapy on Treatment Response in Childhood Arthritis: Results From the UCAN CAN-DU Cohort.

Jelleke B de Jonge, Sytze de Roock, Dieneke Schonenberg-Meinema, J Merlijn van den Berg, Deborah A Marshall, Sebastiaan J Vastert, Rae S M Yeung, Joost F Swart, Susanne M Benseler, UCAN CAN‐DU and UCAN CURE consortia

Abstract readMulticenter Study
In one paragraph

Article in Arthritis & rheumatology (Hoboken, N.J.), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
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  4. Observational
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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

10 authors.

Jelleke B de JongeDivision of Pediatrics, Department of Pediatric Rheumatology, Wilhelmina Children's Hospital, University Medical Center Utrecht, the Netherlands.ORCID 0009-0009-6847-4409
Sytze de RoockDivision of Pediatrics, Department of Pediatric Rheumatology, Wilhelmina Children's Hospital, University Medical Center Utrecht, the Netherlands.ORCID 0009-0003-7281-1304
Dieneke Schonenberg-MeinemaDepartment of Pediatric Immunology, Rheumatology and Infectious Diseases, Emma Children's Hospital, Amsterdam University Medical Centers, University of Amsterdam, the Netherlands.ORCID 0000-0001-9416-6631
J Merlijn van den BergDepartment of Pediatric Immunology, Rheumatology and Infectious Diseases, Emma Children's Hospital, Amsterdam University Medical Centers, University of Amsterdam, the Netherlands.ORCID 0000-0001-9431-5457
Deborah A MarshallDepartments of Community Health Services and Medicine, McCaig Institute for Bone and Joint Health, O'Brien Institute for Public Health, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.ORCID 0000-0002-8467-8008
Sebastiaan J VastertDivision of Pediatrics, Department of Pediatric Rheumatology, Wilhelmina Children's Hospital, University Medical Center Utrecht, the Netherlands.ORCID 0000-0002-4226-0949
Rae S M YeungDivision of Rheumatology, Department of Paediatrics, Immunology and Institute of Medical Science, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada.ORCID 0000-0003-2361-725X
Joost F SwartDivision of Pediatrics, Department of Pediatric Rheumatology, Wilhelmina Children's Hospital, University Medical Center Utrecht, the Netherlands.ORCID 0000-0002-2759-2822
Susanne M BenselerAlberta Children's Hospital Research Institute, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.ORCID 0000-0001-5756-3638
UCAN CAN‐DU and UCAN CURE consortia

Funding

CIHR 381280Dutch Arthritis Foundation (ReumaNederland)Genome AlbertaGenome Canada OGI-150Ontario GenomicsZonMw 001ZonMw 006ZonMw 848
6 · The paper itself

Abstract

objectiveTo estimate the effect of time from symptom onset to start of biologic treatment on achieving inactive arthritis within six months in a cohort of patients with juvenile idiopathic arthritis (JIA).

methodsThe international UCAN CAN-DU study prospectively enrolled patients with JIA across Canada and the Netherlands. A nested cohort study was performed and biologic-naive patients with nonsystemic JIA were included at the start of biologic therapy. The primary outcome was inactive arthritis at six months. Demographics, disease-related parameters, and treatment response were compared using (non)parametric tests among early (time symptom onset to biologic start: 0-6 months), intermediate (7-12 months), and late (13-24 months) treatment groups. A logistic regression model analyzed the effect of time to biologic start on the response at six months, adjusting for active joint count and physician global assessment. A graphical representation of the model was created.

resultsOne hundred and thirty children with JIA were included (early: n = 35; intermediate: n = 46; late: n = 49), 66% were female, and the median age at symptom onset was 11.0 years. The proportion of patients that reach inactive arthritis in the early starters (83%) was significantly higher than in late starters (57%). For each month of delay to the start of biologic treatment, the adjusted odds of having active arthritis after six months of therapy was 1.09 (interquartile range: 1.02-1.17, P = 0.009).

conclusionEarly start of biologic therapies in patients with JIA was associated with a higher proportion of patients reaching inactive arthritis within six months, suggesting a window of opportunity to control disease activity.

Indexed as

Antirheumatic AgentsArthritis, JuvenileBiological ProductsBiological TherapyTime-to-TreatmentAdolescentCanadaChildChild, PreschoolCohort StudiesFemaleHumansMaleNetherlandsProspective StudiesTime FactorsAntirheumatic AgentsBiological Products

Identifiers

PMID40977426
PMCPMC12991923

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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.