TY - JOUR
T1 - Mepolizumab versus benralizumab for eosinophilic granulomatosis with polyangiitis (EGPA)
T2 - A European real-life retrospective comparative study
AU - Mattioli, Irene
AU - Urban, Maria Letizia
AU - Padoan, Roberto
AU - Mohammad, Aladdin J
AU - Salvarani, Carlo
AU - Baldini, Chiara
AU - Berti, Alvise
AU - Cameli, Paolo
AU - Caminati, Marco
AU - Cathébras, Pascal
AU - Bianchi, Fulvia Chieco
AU - Cinetto, Francesco
AU - Cohen Tervaert, Jan Willem
AU - Coppola, Angelo
AU - Costanzo, Giulia
AU - Cottin, Vincent
AU - Crimi, Claudia
AU - Del Giacco, Stefano
AU - Desaintjean, Charlene
AU - Egan, Allyson
AU - Espigol-Frigolé, Georgina
AU - Folci, Marco
AU - Fornaro, Marco
AU - Franceschini, Franco
AU - Govoni, Marcello
AU - Groh, Matthieu
AU - Guarnieri, Gabriella
AU - Hellmich, Bernhard
AU - Iannone, Florenzo
AU - Jones, Rachel
AU - Kernder, Anna
AU - Lo Gullo, Alberto
AU - Lombardi, Carlo
AU - Lopalco, Giuseppe
AU - Losappio, Laura
AU - Marchi, Maria Rita
AU - Rivera, Carlos Martinez
AU - Marvisi, Chiara
AU - Maule, Matteo
AU - Moi, Laura
AU - Monti, Sara
AU - Moosig, Frank
AU - Moroncini, Gianluca
AU - Negrini, Simone Matteo
AU - Neumann, Thomas
AU - Nolasco, Santi
AU - Novikov, Pavel
AU - Roccatello, Dario
AU - Samson, Maxime
AU - Schroeder, Jan Walter
AU - Emmi, Giacomo
AU - European EGPA Study Group
PY - 2025/5
Y1 - 2025/5
N2 - Background: Following the results of the MANDARA trial, this real-life study aimed at comparing the effectiveness and safety profile of mepolizumab versus benralizumab in a European EGPA cohort. Methods: We conducted a retrospective observational comparative study including EGPA patients, who received mepolizumab or benralizumab at the asthma dose. Patients were matched 1:1 by sex, age, BVAS and oral corticosteroid (OCS) dosage at the treatment initiation (T0). Complete response (CR) and partial response (PR), disease activity, OCS, pulmonary parameters, eosinophil count, relapses, and safety outcomes were also compared at 3, 6 and 12 months. Results: Patients treated with mepolizumab or benralizumab (n = 88 each) were matched: 57 % were females, median age was 54 years (IQR 45–60), median OCS dose 10 (7.5–12.5) and 10 (7–13) mg/day, median BVAS 4 (2–7) and 3 (2–8), respectively. 45.4 % of patients in the mepolizumab group and 51.1 % in the benralizumab group achieved CR or PR at T3, with CR steadily increasing during follow-up for both treatments. At T12, a higher CR rate was found in the benralizumab group (48.1 % vs 32.4 %, p = 0.005). No differences in BVAS, OCS, and respiratory parameters were observed between groups at the different timepoints. Throughout the follow-up, both treatments reduced eosinophil count, although a deeper reduction was found in the benralizumab group at all timepoints (p < 0.0001). Safety profile was comparable between patient groups. Conclusion: Mepolizumab and benralizumab showed comparable overall effectiveness and safety in EGPA. However, benralizumab achieved a higher CR rate at T12, and a deeper peripheral eosinophil reduction.
AB - Background: Following the results of the MANDARA trial, this real-life study aimed at comparing the effectiveness and safety profile of mepolizumab versus benralizumab in a European EGPA cohort. Methods: We conducted a retrospective observational comparative study including EGPA patients, who received mepolizumab or benralizumab at the asthma dose. Patients were matched 1:1 by sex, age, BVAS and oral corticosteroid (OCS) dosage at the treatment initiation (T0). Complete response (CR) and partial response (PR), disease activity, OCS, pulmonary parameters, eosinophil count, relapses, and safety outcomes were also compared at 3, 6 and 12 months. Results: Patients treated with mepolizumab or benralizumab (n = 88 each) were matched: 57 % were females, median age was 54 years (IQR 45–60), median OCS dose 10 (7.5–12.5) and 10 (7–13) mg/day, median BVAS 4 (2–7) and 3 (2–8), respectively. 45.4 % of patients in the mepolizumab group and 51.1 % in the benralizumab group achieved CR or PR at T3, with CR steadily increasing during follow-up for both treatments. At T12, a higher CR rate was found in the benralizumab group (48.1 % vs 32.4 %, p = 0.005). No differences in BVAS, OCS, and respiratory parameters were observed between groups at the different timepoints. Throughout the follow-up, both treatments reduced eosinophil count, although a deeper reduction was found in the benralizumab group at all timepoints (p < 0.0001). Safety profile was comparable between patient groups. Conclusion: Mepolizumab and benralizumab showed comparable overall effectiveness and safety in EGPA. However, benralizumab achieved a higher CR rate at T12, and a deeper peripheral eosinophil reduction.
KW - ANCA-associated vasculitis
KW - Benralizumab
KW - Biologicals
KW - Eosinophilic granulomatosis with polyangiitis (EGPA)
KW - Epidemiology
KW - Interleukin-5
KW - Mepolizumab
U2 - 10.1016/j.jaut.2025.103398
DO - 10.1016/j.jaut.2025.103398
M3 - Article
SN - 0896-8411
VL - 153
JO - Journal of Autoimmunity
JF - Journal of Autoimmunity
M1 - 103398
ER -