Rituximab plus methotrexate combination as a salvage therapy in persistently active granulomatosis with polyangiitis.
Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis
/ drug therapy
Antibodies, Antineutrophil Cytoplasmic
Granulomatosis with Polyangiitis
/ drug therapy
Humans
Methotrexate
/ therapeutic use
Remission Induction
Retrospective Studies
Rituximab
/ therapeutic use
Salvage Therapy
Treatment Outcome
ANCA
granulomatosis with polyangiitis
methotrexate
rituximab
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
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 Combination therapy was withdrawn in 4 patients (24%), but never for safety concerns.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
2619-2624Informations 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.