Pediatric rheumatology

Therapeutic Drug Monitoring of Rituximab to Predict Early B-Cell Repopulation in Children With Inflammatory Diseases

J RheumatolPublished Proof-of-concept study

Authors' conclusion

This proof-of-concept study demonstrates that rituximab serum concentration measurements can predict future drug concentrations that are associated with early B-cell repopulation.

Study context

Population
Children and adolescents receiving rituximab for AAV, neuroinflammatory disease or childhood-onset SLE40 samples
Participants
10 children
Outcome
Accuracy of predicted vs measured future rituximab serum concentrations (absolute error)
Methodological detailspharmacokinetic prediction, exponential decay model
  • Pharmacokinetic prediction
  • Exponential decay model

Main finding

As reported in the abstract

Rituximab half-life, median (range 1.7-3.5)

2.7 weeks

Absolute error of predictions, median (IQR −0.02 to 0.26); slight overestimation

0.12 μg/mL

Time to minimum concentration for B-cell depletion (0.55 μg/mL), median (range 13.3-28.8)

22.2 weeks

Participants with B-cell repopulation, at concentrations ≤ 0.3 μg/mL

5

Further findings

Participants with positive antidrug antibodies (half-life 1.8 weeks)
1

Original publication

Therapeutic Drug Monitoring of Rituximab to Predict Early B-Cell Repopulation in Children With Inflammatory Diseases. J Rheumatol. Published 1 March 2026. doi:10.3899/jrheum.2025-0890

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