Pediatric rheumatology

Toward a Treat‐to‐Target Strategy in Juvenile Dermatomyositis: What Are the Suitable Targets and Optimal Timing of Their Achievement?

Arthritis RheumatolPublished Retrospective cohort study

Authors' conclusion

This study provides real-world data for potential timelines to target with a treat-to-target strategy for JDM.

Study context

Population
Patients with physician-confirmed juvenile dermatomyositis (JDM) at two tertiary care centres, first two years after diagnosis (mean age at diagnosis 8 years)
Participants
187 patients2 sites
Exposure
Gaslini (Gaslini) vs SickKids
Outcome
Time to treatment response (normalisation of muscle enzymes, muscle remission, skin remission, inactive disease)
Follow-up
First two years following diagnosis
Methodological detailstwo tertiary care centres, Kaplan-Meier survival analysis
  • Two tertiary care centres
  • Kaplan-Meier survival analysis

Main finding

As reported in the abstract

Time to treatment response
Normalisation of muscle enzymes, on average, after treatment initiation
three months
Muscle remission, on average, after treatment initiation
six months
Skin remission, after starting treatment
within 12 months

Observational data: associations, not effects.

Further findings

Time to inactive disease (varied between sites)

Original publication

Toward a Treat‐to‐Target Strategy in Juvenile Dermatomyositis: What Are the Suitable Targets and Optimal Timing of Their Achievement? Arthritis Rheumatol. Published 28 January 2026. doi:10.1002/art.43431

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