Rituximab plus methotrexate combination as a salvage therapy in persistently active granulomatosis with polyangiitis

Author:

Sorin Boris1ORCID,Samson Maxime2,Durel Cécile-Audrey3,Diot Elisabeth4,Guichard Isabelle5,Grados Aurélie6,Limal Nicolas7,Régent Alexis1,Cohen Pascal1,Dion Jérémie1ORCID,Legendre Paul1,Le Guern Véronique1,Mouthon Luc1,Guillevin Loïc1,Terrier Benjamin1

Affiliation:

1. Department of Internal Medicine, Hôpital Cochin, Paris

2. Department of Internal Medicine and Clinical Immunology, Dijon University Hospital, Dijon

3. Department of Internal Medicine, Hôpital Edouard Herriot, Hospices Civils de Lyon, Lyon

4. Department of Internal Medicine, Hôpital Bretonneau, Tours

5. Department of Internal Medicine, Centre Hospitalier Universitaire de Saint-Etienne, Saint-Etienne

6. Department of Internal Medicine, Centre Hospitalier de Niort, Niort

7. Department of Internal Medicine, Hôpital Henri Mondor, Créteil, France

Abstract

Abstract Objective The aim of this study was to describe the efficacy and safety of rituximab and MTX (RTX/MTX) combination therapy in ANCA-associated vasculitides (AAV). Methods A retrospective French nationwide study was conducted in patients with AAV who received RTX/MTX combination therapy for persistently active disease. Results Seventeen patients were included. All patients had granulomatosis with polyangiitis (GPA), with positive ANCA in 76% of them, mainly with PR3-ANCA specificity. Sixteen patients (94%) had priorly failed to achieve remission with RTX and 11 (65%) with CYC. Patients had experienced a median of 3 (2–4) flares. Manifestations requiring RTX/MTX combination therapy were subglottic or bronchial stenosis in 6 patients (35%), orbital mass in 6 (35%), disabling ENT involvement in 2 (12%), and epiduritis and pachymeningitis in 1 case (6%) each. The median follow-up duration for the RTX/MTX combination therapy was 11 months (11–26 months). At 6 months, global response had been achieved in 15 patients (88%), including partial response in 11 (65%) and complete response in 4 (24%). At last evaluation, global response had been achieved in 16 patients (94%). Seven patients (41%) experienced severe adverse events (grade 3 or 4), including infections in 4 (24%) and hepatitis in 2 (12%). Combination therapy was withdrawn in 4 patients (24%), but never for safety concerns. In contrast, the MTX dose was decreased in 2 patients (12%) because of adverse events. One patient died of an unknown cause. Conclusion RTX/MTX combination therapy could be an effective salvage therapy to treat persistently active GPA with granulomatous manifestations, with an acceptable safety profile.

Publisher

Oxford University Press (OUP)

Subject

Pharmacology (medical),Rheumatology

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