Evidence map›Paper›PMID 40275364›Full record

ArticlePediatric rheumatology online journal2025

Incidence and reasons for biologic and targeted synthetic DMARD switching in juvenile idiopathic arthritis: a real- life stratified analysis.

Daniel Clemente, Leticia Leon, Juan Carlos Nieto-Gonzalez, Alina Lucica Boteanu, Laura Trives Folguera, Antía Asunción García-Fernández, Helena Amar Muñoz, Aliuska Palomeque, Juan Carlos López Robledillo, Lydia Abasolo

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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. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Daniel ClementePediatric Rheumatology Unit, Hospital Universitario Niño Jesús, Madrid, Spain.ORCID http://orcid.org/0000-0002-1605-7488
Leticia LeonFaculty of Health Sciences-HM Hospitals, Universidad Camilo José Cela, Madrid, Spain. lleon.hcsc@salud.madrid.org.ORCID http://orcid.org/0000-0001-7142-0545
Juan Carlos Nieto-GonzalezRheumatology Department, Hospital General Universitario Gregorio Marañón, Madrid, Spain.ORCID http://orcid.org/0000-0002-5971-4185
Alina Lucica BoteanuRheumatology Department, Hospital General Universitario Ramon y Cajal, Madrid, Spain.ORCID http://orcid.org/0000-0002-7826-6947
Laura Trives FolgueraRheumatology Department, Hospital Universitario Infanta Sofía, San Sebastián de los Reyes, Spain.ORCID http://orcid.org/0000-0002-7258-8136
Antía Asunción García-FernándezRheumatology Department, Hospital General Universitario Ramon y Cajal, Madrid, Spain.ORCID http://orcid.org/0000-0003-3670-6796
Helena Amar MuñozRheumatology Department, Hospital General Universitario Gregorio Marañón, Madrid, Spain.ORCID http://orcid.org/0009-0002-6231-1747
Aliuska PalomequeRheumatology Department, Hospital General Universitario Ramon y Cajal, Madrid, Spain.ORCID http://orcid.org/0009-0001-4064-448X
Juan Carlos López RobledilloPediatric Rheumatology Unit, Hospital Universitario Niño Jesús, Madrid, Spain.ORCID http://orcid.org/0000-0002-5253-945X
Lydia AbasoloMusculoskeletal Pathology Group, Rheumatology Department, Health Research Institute (IdISSC), Hospital Clínico San Carlos, Madrid, Spain.ORCID http://orcid.org/0000-0001-8152-0478

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSwitching biologic and targeted synthetic DMARDs (b/tsDMARD) is common in juvenile idiopathic arthritis (JIA) patients, though information about how this switching is done is scarce. This study aimed to determine the incidence rate, reasons for switching, and risk factors associated with switching due to inefficacy across different JIA subtypes.

methodsA multi-hospital electronic health record (EHR) registry was used to identify JIA patients prescribed ≥ 1 b/tsDMARD between 2000 and 2024. Patients were categorized into four JIA subgroups: oligoarticular, polyarticular, juvenile spondyloarthritis (JSpA), and systemic JIA. The primary outcomes were switching rates and switching due to inefficacy. Incidence rates (IR) were calculated per 100 patients-year. Cox multivariate regression analyses were run to assess the risk of b/tsDMARDs switching due to inefficacy, expressed as hazard ratio (HR) and 95% CI.

resultsIn our JIA registry, a total of 213 patients received a b/tsDMARD, with a total of 321 courses. The mean age at onset was 6.03 ± 4.44 years and 66.20% were females. The oligoarticular course group included 69 patients (32.39%), the polyarticular group 76 patients (35.68%), the JSpA group 43 patients (20.19%), and the systemic group 25 patients (11.74%). We found a total of 100 b/tsDMARD switches, with 32.05% of patients switched at least once. The systemic JIA group was more likely to swapping (p ≤ 0.001). Through the study period, the overall switching incidence rate was 7.32 [6.01-8.90] per 100 patients-year. In the stratified analysis across JIA groups, the systemic JIA group exhibited the highest incidence (IR:17.01 [11.20-25.84]). Regarding switching due to inefficacy, global incidence was 4.53 [3.53-5.82] and again systemic JIA was the group with the highest incidence (IR: 9.28 [5.27-16.34]). Still, the adjusted multivariate final model confirms that systemic JIA needed more switching due to inefficacy (2.43 [1.01-5.89], p = 0.04).

conclusionThis real-life study provides data on different switch patterns in various subtypes of JIA, confirming that patients with systemic JIA needed more switching, did more swapping strategies, and had more risk for switching due to inefficacy.

Indexed as

Antirheumatic AgentsArthritis, JuvenileBiological ProductsDrug SubstitutionAdolescentChildChild, PreschoolFemaleHumansIncidenceMaleRegistriesAntirheumatic AgentsBiological ProductsBiologic and targeted synthetic DMARDsIncidenceJuvenile idiopathic arthritisRisk factorsSwitching

Identifiers

PMID40275364
PMCPMC12023536

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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.