# Long-term effectiveness and safety of benralizumab in EGPA: a 3-year single-center experience

## TL;DR

This study shows that benralizumab is effective and safe for treating a severe form of asthma called EGPA over three years.

## Contribution

The study provides new evidence on the long-term effectiveness and safety of benralizumab in treating EGPA.

## Key findings

- Benralizumab increased clinical remission rates from 39.4% at 3 months to 65.0% at 36 months.
- Corticosteroid use dropped from 90.9% to 15.4%, and eosinophil counts decreased significantly.
- Drug retention rates were 81.8% at 1 year and 62.4% at 3 years, with mild adverse events reported.

## Abstract

Benralizumab emerged as a promising treatment option for eosinophilic granulomatosis with polyangiitis (EGPA). This study assessed the long-term effectiveness and safety of benralizumab in patients with severe asthma and relapsing-refractory EGPA.

This retrospective, single-center study evaluated patients treated with benralizumab (30 mg/8 weeks), followed for up to 36 months. Primary outcome included disease remission (defined as Birmingham Vasculitis Activity Score version 3 = 0 and prednisone dose ≤4 mg/day). Secondary endpoints were corticosteroid tapering, lung function, relapses, treatment failure and drug retention rates.

The study included 33 EGPA patients (17 [51.5%] male; median age at benralizumab initiation 56 years [IQR: 47–62]). Before starting benralizumab, most patients were on corticosteroids (90.9%), prior treatments included mepolizumab (24.2%). Benralizumab showed effectiveness, with clinical remission rates increasing from 39.4% (95% CI: 22.9–57.9) at 3 months to 65.0% (95% CI: 40.8–84.6) at 36 months (p < 0.001). Corticosteroid use declined from 90.9% to 15.4%, eosinophil counts dropped from 850 (515–1367) to 0 (0–0) cells/µL, and BVASv3 decreased from 2 (2–5) to 0 (0–0), showing significant improvements (p = 0.002 and p < 0.001, respectively). Proportion of patients experiencing asthma exacerbations reduced, alongside improved lung function. Retention rates were 81.8% at 1 year, 72.6% at 2 years, and 62.4% at 3 years, with secondary failure due to uncontrolled sinonasal symptoms. Mild adverse events were observed in 21.2% of patients.

These findings support the long-term effectiveness and safety of benralizumab for EGPA, highlighting its role in inducing clinical remission, reducing corticosteroid dependence, and controlling disease activity.