Long-term efficacy and safety of rituximab in IgG4-related disease: Data from a French nationwide study of thirty-three patients

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Ebbo, Mikael | Grados, Aurelie | Samson, Maxime | Groh, Matthieu | Loundou, Anderson | Rigolet, Pierre | Terrier, Benjamin | Guillaud, Constance | Carra-Dallière, Clarisse | Renou, Frédéric | Pozdzik, Agnieszka | Labauge, Pierre | Palat, Sylvain | Berthelot, Jean-Marie | Pennaforte, Jean-Loup | Wynckel, Alain | Lebas, Céline | Le Gouellec, Noémie | Quemeneur, Thomas | Dahan, Karine | Carbonnel, Franck | Leroux, Gaëlle | Perlat, Antoinette | Mathian, Alexis | Cacoub, Patrice | Hachulla, Eric | Costedoat-Chalumeau, Nathalie | Harlé, Jean-Robert | Schleinitz, Nicolas

Edité par CCSD ; Public Library of Science -

International audience. Objectives: To assess efficacy and safety of rituximab (RTX) as induction therapy, maintenance of remission and treatment of relapses in a cohort of IgG4-related disease (IgG4-RD) patients.Methods: Nationwide retrospective multicenter study of IgG4-RD patients treated with at least one course of RTX. Clinical, biological and radiological response, relapse rate and drug tolerance were analyzed. Kaplan-Meier curves were plotted and risk factors for relapse studied with a Cox regression model.Results: Among 156 IgG4-RD patients included in the French database, 33 received rituximab. Clinical response was noted in 29/31 (93.5%) symptomatic patients. Glucocorticoids withdrawal was achieved in 17 (51.5%) patients. During a mean follow-up of 24.8 ±21 months, 13/31 (41.9%) responder patients relapsed after a mean delay of 19 ±11 months after RTX. Active disease, as defined by an IgG4-RD Responder Index >9 before RTX, was significantly associated with relapse (HR = 3.68, 95% CI: 1.1, 12.6) (P = 0.04), whereas maintenance therapy with systematic (i.e. before occurrence of a relapse) RTX retreatment was associated with longer relapse-free survival (41 versus 21 months; P = 0.02). Eight severe infections occurred in 4 patients during follow-up (severe infections rate of 12.1/100 patient-years) and hypogammaglobulinemia ≤5 g/l in 3 patients.Conclusion: RTX is effective for both induction therapy and treatment of relapses in IgG4-RD, but relapses are frequent after B-cell reconstitution. Maintenance therapy with systematic RTX infusions is associated with longer relapse-free survival and might represent a novel treatment strategy. Yet, the high rate of infections and the temporary effect of RTX might be hindrances to such strategy.

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