Publikation

Mepolizumab for Eosinophilic Granulomatosis with Polyangiitis (EGPA): a European multicenter observational study

Wissenschaftlicher Artikel/Review - 04.08.2021

Bereiche
PubMed
DOI

Zitation
European EGPA Study Group, Moroni L, Fagni F, Bello F, Fiori D, Ribi C, Cohen Tervaert J, Bargagli E, Samson M, Hellmich B, Mohammad A, Vacca A, Roccatello D, Ramirez G, Nasser M, Emmi G, Vaglio A, Prisco D, Jayne D, Salvarani C, Iannone F, Seeliger B, Egan A, Padoan R, Firinu D, Toniati P, Marvisi C, Fraticelli P, Cinetto F, Berti A, Lombardi C, Baldini C, Novikov P, Lopalco G, Neumann T, Schiavon F, Del Giacco S, Franceschini F, Cottin V, Dagna L, Urban M, Alberici F, Folci M, Crimi C, Silvagni E, Monti S, Kernder A, Schroeder J, Espígol-Frigolé G, Moosig F, Parronchi P, Lunardi C, Quartuccio L, Sinico R, Negrini S, Bettiol A. Mepolizumab for Eosinophilic Granulomatosis with Polyangiitis (EGPA): a European multicenter observational study. Arthritis Rheumatol 2021
Art
Wissenschaftlicher Artikel/Review (Englisch)
Zeitschrift
Arthritis Rheumatol 2021
Veröffentlichungsdatum
04.08.2021
eISSN (Online)
2326-5205
Kurzbeschreibung/Zielsetzung

OBJECTIVE
Mepolizumab proved efficacious for eosinophilic granulomatosis with polyangiitis (EGPA, former Churg-Strauss) at the dosage of 300mg/4 weeks in the randomized controlled MIRRA trial. Few successful real-life experiences with the dosage approved for severe eosinophilic asthma (100mg/4 weeks) were recently reported. We retrospectively assessed the effectiveness and safety of mepolizumab 100 and 300mg/4 weeks in a large European EGPA cohort.

METHODS
We included all EGPA patients treated with mepolizumab at the recruiting centres in 2015-2020. Treatment response was evaluated from month 3 through 24 (T3-T24) after mepolizumab starting. Complete response (CR) was defined as no disease activity (Birmingham Vasculitis Activity Score, BVAS=0) and a prednisone dose ≤4mg/day. Respiratory outcomes included asthma and ear-nose-throat (ENT) exacerbations.

RESULTS
We included 203 patients, of whom 191 at stable dosage (158 mepolizumab 100mg/4 weeks, 33 300mg/4 weeks). At T3, 25 patients (12.3%) had a CR. CR rates increased to 30.4% and 35.7% at T12 and T24 and were comparable between mepolizumab 100 and 300mg/4 weeks. Mepolizumab led to a significant reduction in BVAS, prednisone dose, eosinophil counts from T3 through T24, with no significant differences between 100 and 300 mg/4weeks. Eighty-two patients (40.4%) experienced asthma exacerbations [57/158 (36%) on 100mg/4 weeks; 17/33 (52%) on 300mg/4 weeks]. Thirty-one (15.3%) experienced ENT exacerbations. Forty-four patients (21.7%) experienced adverse events, most being non-serious (38/44).

CONCLUSION
Mepolizumab both at 100 and 300mg/4 weeks is effective for EGPA. The two dosages should be compared in the setting of a controlled trial.