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


Journal

Rheumatology (Oxford, England)
ISSN: 1462-0332
Titre abrégé: Rheumatology (Oxford)
Pays: England
ID NLM: 100883501

Informations de publication

Date de publication:
30 05 2022
Historique:
received: 23 07 2021
revised: 20 10 2021
pubmed: 27 10 2021
medline: 3 6 2022
entrez: 26 10 2021
Statut: ppublish

Résumé

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). A retrospective French nationwide study was conducted in patients with AAV who received RTX/MTX combination therapy for persistently active disease. 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 Combination therapy was withdrawn in 4 patients (24%), but never for safety concerns.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. RTX/MTX combination therapy could be an effective salvage therapy to treat persistently active GPA with granulomatous manifestations, with an acceptable safety profile.

Identifiants

pubmed: 34698818
pii: 6410656
doi: 10.1093/rheumatology/keab791
doi:

Substances chimiques

Antibodies, Antineutrophil Cytoplasmic 0
Rituximab 4F4X42SYQ6
Methotrexate YL5FZ2Y5U1

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2619-2624

Informations de copyright

© The Author(s) 2021. Published by Oxford University Press on behalf of the British Society for Rheumatology. All rights reserved. For permissions, please email: journals.permissions@oup.com.

Auteurs

Boris Sorin (B)

Department of Internal Medicine, Hôpital Cochin, Paris.

Maxime Samson (M)

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

Cécile-Audrey Durel (CA)

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

Elisabeth Diot (E)

Department of Internal Medicine, Hôpital Bretonneau, Tours.

Isabelle Guichard (I)

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

Aurélie Grados (A)

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

Nicolas Limal (N)

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

Alexis Régent (A)

Department of Internal Medicine, Hôpital Cochin, Paris.

Pascal Cohen (P)

Department of Internal Medicine, Hôpital Cochin, Paris.

Jérémie Dion (J)

Department of Internal Medicine, Hôpital Cochin, Paris.

Paul Legendre (P)

Department of Internal Medicine, Hôpital Cochin, Paris.

Véronique Le Guern (V)

Department of Internal Medicine, Hôpital Cochin, Paris.

Luc Mouthon (L)

Department of Internal Medicine, Hôpital Cochin, Paris.

Loïc Guillevin (L)

Department of Internal Medicine, Hôpital Cochin, Paris.

Benjamin Terrier (B)

Department of Internal Medicine, Hôpital Cochin, Paris.

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Classifications MeSH