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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TitreLong-term efficacy and safety of rituximab in IgG4-related disease: Data from a French nationwide study of thirty-three patients
Type de publicationJournal Article
Year of Publication2017
AuteursEbbo M, Grados A, Samson M, Groh M, Loundou A, Rigolet A, Terrier B, Guillaud C, Carra-Dalliere C, Renou F, Pozdzik A, Labauge P, Palat S, Berthelot J-M, Pennaforte J-L, Wynckel A, Lebas C, Le Gouellec N, Quemeneur T, Dahan K, Carbonnel F, Leroux G, Perlat A, Mathian A, Cacoub P, Hachulla E, Costedoat-Chalumeau N, Harle J-R, Schleinitz N
JournalPLOS ONE
Volume12
Paginatione0183844
Date PublishedSEP 15
Type of ArticleArticle
ISSN1932-6203
Résumé

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 patientyears) 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.

DOI10.1371/journal.pone.0183844