Comparative real-world effectiveness and safety of benralizumab and two mepolizumab dosing regimens in eosinophilic granulomatosis with polyangiitis: a 24-month prospective single-center cohort study - Summary - MDSpire

Comparative real-world effectiveness and safety of benralizumab and two mepolizumab dosing regimens in eosinophilic granulomatosis with polyangiitis: a 24-month prospective single-center cohort study

  • By

  • Marta Codirenzi

  • Federica Davanzo

  • Luca Iorio

  • Eleonora Fiorin

  • Gabriella Guarnieri

  • Fulvia Chieco Bianchi

  • Alessia Achille

  • Maria Rita Marchi

  • Andrea Vianello

  • Andrea Doria

  • Roberta Ramonda

  • Roberto Padoan

  • June 15, 2026

  • 0 min

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Objective:

To evaluate the effectiveness and safety of benralizumab compared to two mepolizumab dosing strategies in patients with eosinophilic granulomatosis with polyangiitis (EGPA) over 24 months.

Key Findings:
  • Remission rates at 24 months were 73.7% for benralizumab, 81.0% for mepolizumab 300 mg, and 50.0% for mepolizumab 100 mg, with no significant differences reported.
  • GC-free status reached 63.2% with benralizumab, 85.7% with mepolizumab 300 mg, and 58.3% with mepolizumab 100 mg at 24 months, with no significant between-group differences.
  • Eosinophil counts decreased significantly, with near-complete suppression in the benralizumab group, indicating a strong therapeutic effect.
  • Pulmonary function improved, particularly in the benralizumab group, suggesting enhanced respiratory outcomes.
  • Adverse events were uncommon, with no serious events reported, indicating a favorable safety profile.
Interpretation:

The study indicates that anti–IL-5/IL-5R biologics are effective and well tolerated in EGPA, with a significant glucocorticoid-sparing effect, which may influence treatment strategies.

Limitations:
  • The observational design may introduce confounding by indication, potentially biasing the effectiveness results.
  • Comparative effectiveness conclusions are limited due to the study's design, which may not account for all variables influencing treatment outcomes.
Conclusion:

Findings support individualized biologic selection in EGPA, highlighting the effectiveness of both benralizumab and mepolizumab dosing strategies.

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