Real-world comparison of lymphopenia profiles in S1P receptor modulators for multiple sclerosis: a multicenter retrospective study.
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Maniscalco Giorgia Teresa, Sparaco Maddalena, Di Gregorio Maria, Cafasso Giuseppina, Signoriello Elisabetta, Romano Felice, Iodice Rosa, Fantozzi Roberta, Bellantonio Paolo, Zanghi Aurora, Sinisi Leonardo, D'Ambrosio Alessandro, Busillo Vincenzo, Scarano Valentina, Capuano Rocco, Lavorgna Luigi, Williams Michela, De Martino Antonio, Di Battista Maria Elena, Di Giulio Cesare Daniele, Lus Giacomo, Cassano Emanuele, Di Filippo Paola Sofia, Sibilia Grazia, Abbadessa Gianmarco, Andreone Vincenzo, Bonavita Simona
Аннотация
METHODS: We conducted a retrospective multicenter study across thirteen MS centers in Italy, including 191 MS patients (mean age 46.4 years; 61.3% women). Of these, 28.8% received Siponimod, 26.2% Ozanimod, 24.1% Fingolimod, and 20.9% Ponesimod. Lymphocyte counts were measured at baseline (T0), one month (T1), three months (T3), and six months (T6) post-treatment. Lymphopenia grades range from 0 (≥ 1.0 × 10^9 cells/L) to 4 (< 0.2 × 10^9 cells/L), according to Common Terminology Criteria for Adverse Events.
RESULTS: At T1, Ozanimod showed a significantly higher mean lymphocyte count than Siponimod and Fingolimod (p < 0.001), Ponesimod higher mean lymphocyte count than Siponimod (p = 0.006). The differences persisted between Ozanimod than Siponimod and Fingolimod at T3 (p = 0.01 and p = 0.04), and between Ponesimod and Siponimod at T6 (p = 0.03). Severe lymphopenia cases were significantly higher in Siponimod than in Ponesimod and Ozanimod, at T1 (p = 0.001 and p = 0.0001). The differences remained significant between Ozanimod and Siponimod, at T3 (p = 0.001), and between Ponesimod and Siponimod, Fingolimod and Ozanimod, at T6 (p = 0.001). Grade 4 lymphopenia was observed in Ozanimod and Siponimod at T3.
CONCLUSION: This is the first real-world, head-to-head observational study comparing lymphopenia among different S1P modulators. Our results might assist in therapy choice depending on patients baseline hematological characteristics.