Comparative Efficacy of Nonsteroid Immunosuppressive Medications in Childhood Nephrotic Syndrome

Cal H Robinson1,2,3, Nowrin Aman3, Tonny Banh3

  • 1Division of Nephrology, The Hospital for Sick Children, Toronto, Ontario, Canada.

JAMA Pediatrics
|January 27, 2025
PubMed

Insights

For children with nephrotic syndrome, cyclophosphamide and calcineurin inhibitors showed no significant difference in preventing relapses. Cyclophosphamide is more accessible globally.

Area of Science:

  • Pediatric Nephrology
  • Immunosuppressive Therapy
  • Chronic Inflammatory Conditions

Background:

  • Cyclophosphamide and calcineurin inhibitors are widely used for pediatric chronic inflammatory conditions.
  • Their comparative effectiveness in childhood nephrotic syndrome is unclear, causing practice variations.
  • Nephrotic syndrome is a common kidney disease in children, and suboptimal treatment increases morbidity.

Purpose of the Study:

  • To compare the effectiveness of cyclophosphamide versus calcineurin inhibitors (tacrolimus or cyclosporine) in preventing relapses of childhood nephrotic syndrome.

Main Methods:

  • Emulated a pragmatic, open-label trial using data from the INSIGHT prospective cohort study (1996-2019).
  • Included children (1-18 years) with steroid-sensitive nephrotic syndrome initiating either cyclophosphamide or a calcineurin inhibitor.
  • Used overlap weighting for propensity scores to emulate randomization; analyzed time to relapse using weighted Kaplan-Meier and Cox models.

Main Results:

  • No significant difference in time to relapse between calcineurin inhibitor and cyclophosphamide treatment (HR, 1.25; 95% CI, 0.84-1.87).
  • Relapse rates were numerically higher with calcineurin inhibitors (85% vs 73%), but not statistically significant.
  • Calcineurin inhibitor use was associated with more hospitalizations and intravenous albumin use.

Conclusions:

  • No evidence of a difference in relapse prevention between cyclophosphamide and calcineurin inhibitors for childhood nephrotic syndrome.
  • Cyclophosphamide offers a shorter treatment duration and greater global accessibility.
  • Further research may clarify optimal immunosuppressive strategies for this condition.
Abstract

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