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 - Report - MDSpire
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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
Clinical Report: Real-World Assessment of Benralizumab Versus Mepolizumab in EGPA
Overview
This study evaluates the effectiveness of benralizumab and two dosing strategies of mepolizumab in patients with eosinophilic granulomatosis with polyangiitis (EGPA) over 24 months. Results indicate that both treatment regimens are effective in achieving remission and glucocorticoid-free status, with no significant differences between them.
Background
Eosinophilic granulomatosis with polyangiitis (EGPA) is a rare but serious condition characterized by asthma and vasculitis, often requiring long-term glucocorticoid therapy. The introduction of anti–IL-5 and anti–IL-5 receptor biologics offers a promising steroid-sparing approach, particularly for patients with relapsing or refractory disease. Understanding the comparative effectiveness of these biologics is crucial for optimizing treatment strategies.
Data Highlights
Treatment
Remission Rate at 24 Months
GC-Free Status at 24 Months
Benralizumab 30 mg
73.7% (14/19)
63.2% (12/19)
Mepolizumab 300 mg
81.0% (17/21)
85.7% (18/21)
Mepolizumab 100 mg
50.0% (6/12)
58.3% (7/12)
Key Findings
Remission rates at 24 months were 73.7% for benralizumab and 81.0% for mepolizumab 300 mg.
GC-free status was achieved by 63.2% of patients on benralizumab and 85.7% on mepolizumab 300 mg.
Eosinophil counts decreased significantly, with near-complete suppression observed in the benralizumab group.
Improvement in pulmonary function indices was most pronounced in the benralizumab cohort.
Discontinuations were primarily due to inadequate control of ENT or respiratory symptoms.
Clinical Implications
The findings support the use of both benralizumab and mepolizumab as effective treatment options for EGPA, with significant potential for glucocorticoid sparing. Clinicians should consider individual patient profiles when selecting a biologic therapy, as both options demonstrate similar efficacy.
Conclusion
This study highlights the effectiveness and tolerability of anti–IL-5/IL-5R biologics in EGPA over a 24-month period, reinforcing the need for personalized treatment approaches in this patient population.
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
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