Arthritis Research & Therapy · 2021 · 38 citations · 14 references
Life SciencesPharmacologyPharmacotherapyImmunopharmacologyImmunotherapyRheumatologyAutoimmune DiseasesAutoimmune Rheumatic DiseasesCorticosteroid TherapyEosinophilic DisordersGranulomatous InflammationImmunosuppressionAnti-interleukin 5 TherapyClinical RemissionDisease Activity MeasurementEosinophil CountEosinophilic Disease TherapyEosinophilic InfiltratesTherapeutic CorticosteroidsVasculitis Activity Assessment
BACKGROUND: Mepolizumab (MPZ), an anti-interleukin-5 antibody, is effective for the treatment of eosinophilic granulomatosis with polyangiitis (EGPA). However, its effectiveness has not been adequately evaluated in real-world clinical practice. In this study, we assessed the effectiveness and safety of MPZ (300 mg) for relapsing/refractory EGPA resistant to corticosteroids (CS) for 1 year in real-world settings. METHODS: We administered MPZ (300 mg) to 16 patients with relapsing/refractory EGPA resistant to CS (Post-MPZ). We also retrospectively collected data from the same patients for the 12 months before the administration of MPZ (Pre-MPZ). The primary endpoint was the 12-month remission rate after MPZ administration and the secondary endpoints were the Birmingham vasculitis activity score (BVAS), vasculitis damage index (VDI), eosinophil counts, changes in concomitant CS doses/concomitant immunosuppressant use, MPZ retention rate, and incidence of adverse events. The clinical course was compared between Pre-MPZ and Post-MPZ. RESULTS: The 12-month remission rate after the initiation of MPZ was 75%. No change was observed in BVAS, eosinophil count, or concomitant CS dose over time in the Pre-MPZ group, whereas all these parameters were significantly decreased over time in the Post-MPZ group. The number of patients using concomitant immunosuppressant also decreased over time in the Post-MPZ group. VDI did not increase in either group. The MPZ retention rate was 100% and only three patients (18.8%) had infections. Changes in BVAS, eosinophil count, and cumulative concomitant CS dose were significantly lower in the Post-MPZ group than in the Pre-MPZ group. There was no significant difference in the changes in VDI between the groups. CONCLUSION: This study demonstrated that MPZ is effective and safe for EGPA. Furthermore, MPZ decreases disease activity, increases remission rate, and has a CS-sparing effect.
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Allergic granulomatosis, allergic angiitis, and periarteritis nodosa.
Jacob Churg, Lotte Strauss · PubMed · 2004 · 1.7K citations
Modification and validation of the Birmingham Vasculitis Activity Score (version 3)
Chetan Mukhtyar, R Lee, Denise Scott Brown et al. · Annals of the Rheumatic Diseases · 2008 · 1.2K citations
Medicine, Cancer Biology, Oncology +14