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Efficacy and safety of rituximab as maintenance therapy for relapsing granulomatosis with polyangiitis—a case series

The objective of this work was to study the efficacy and safety of pre-emptive rituximab (RTX) in a series of patients with severe relapsing granulomatosis with polyangiitis (GPA). GPA is a systemic vasculitis with a high relapse rate despite successful remission induction. Drug toxicity with repeat...

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Autores principales: Knight, A., Hallenberg, H., Baecklund, E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer London 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4058072/
https://www.ncbi.nlm.nih.gov/pubmed/23959445
http://dx.doi.org/10.1007/s10067-013-2351-y
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author Knight, A.
Hallenberg, H.
Baecklund, E.
author_facet Knight, A.
Hallenberg, H.
Baecklund, E.
author_sort Knight, A.
collection PubMed
description The objective of this work was to study the efficacy and safety of pre-emptive rituximab (RTX) in a series of patients with severe relapsing granulomatosis with polyangiitis (GPA). GPA is a systemic vasculitis with a high relapse rate despite successful remission induction. Drug toxicity with repeated induction treatments and long-standing immunosuppression poses a problem. Based on the findings in reports on RTX for rheumatoid arthritis, we treated patients with severe relapsing GPA with pre-emptive RTX, 1,000 mg 2 weeks apart every 6 months, aiming at achieving sustainable remission. All patients at one centre with relapsing GPA in spite of traditional maintenance treatment, who had received more than or equal to three cycles of RTX as regularly repeated pre-emptive maintenance therapy every 6 months, were included in this retrospective study. Information on disease manifestations and activity, treatments, lab parameters and adverse events was extracted from the medical files. Of the 12 included patients, all with a positive proteinase 3–anti-neutrophil cytoplasmic antibodies, generalised disease and a median disease duration of 35 months (21–270), 92 % (11/12) achieved sustainable remission during a median follow-up time of 32 months (range 21–111) from first RTX treatment. Concomitant immunosuppressants were reduced. Infections were the most common adverse events, but infections were an issue also before the start of RTX. RTX administered every 6 months seems to be an effective maintenance treatment in a population with severe, relapsing long-standing GPA. Granulomatous as well as vasculitic manifestations responded equally well. Infections are a problem in this patient group but no new safety problems were identified.
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spelling pubmed-40580722014-06-18 Efficacy and safety of rituximab as maintenance therapy for relapsing granulomatosis with polyangiitis—a case series Knight, A. Hallenberg, H. Baecklund, E. Clin Rheumatol Original Article The objective of this work was to study the efficacy and safety of pre-emptive rituximab (RTX) in a series of patients with severe relapsing granulomatosis with polyangiitis (GPA). GPA is a systemic vasculitis with a high relapse rate despite successful remission induction. Drug toxicity with repeated induction treatments and long-standing immunosuppression poses a problem. Based on the findings in reports on RTX for rheumatoid arthritis, we treated patients with severe relapsing GPA with pre-emptive RTX, 1,000 mg 2 weeks apart every 6 months, aiming at achieving sustainable remission. All patients at one centre with relapsing GPA in spite of traditional maintenance treatment, who had received more than or equal to three cycles of RTX as regularly repeated pre-emptive maintenance therapy every 6 months, were included in this retrospective study. Information on disease manifestations and activity, treatments, lab parameters and adverse events was extracted from the medical files. Of the 12 included patients, all with a positive proteinase 3–anti-neutrophil cytoplasmic antibodies, generalised disease and a median disease duration of 35 months (21–270), 92 % (11/12) achieved sustainable remission during a median follow-up time of 32 months (range 21–111) from first RTX treatment. Concomitant immunosuppressants were reduced. Infections were the most common adverse events, but infections were an issue also before the start of RTX. RTX administered every 6 months seems to be an effective maintenance treatment in a population with severe, relapsing long-standing GPA. Granulomatous as well as vasculitic manifestations responded equally well. Infections are a problem in this patient group but no new safety problems were identified. Springer London 2013-08-20 2014 /pmc/articles/PMC4058072/ /pubmed/23959445 http://dx.doi.org/10.1007/s10067-013-2351-y Text en © The Author(s) 2013 https://creativecommons.org/licenses/by-nc/2.0/ Open Access This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Original Article
Knight, A.
Hallenberg, H.
Baecklund, E.
Efficacy and safety of rituximab as maintenance therapy for relapsing granulomatosis with polyangiitis—a case series
title Efficacy and safety of rituximab as maintenance therapy for relapsing granulomatosis with polyangiitis—a case series
title_full Efficacy and safety of rituximab as maintenance therapy for relapsing granulomatosis with polyangiitis—a case series
title_fullStr Efficacy and safety of rituximab as maintenance therapy for relapsing granulomatosis with polyangiitis—a case series
title_full_unstemmed Efficacy and safety of rituximab as maintenance therapy for relapsing granulomatosis with polyangiitis—a case series
title_short Efficacy and safety of rituximab as maintenance therapy for relapsing granulomatosis with polyangiitis—a case series
title_sort efficacy and safety of rituximab as maintenance therapy for relapsing granulomatosis with polyangiitis—a case series
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4058072/
https://www.ncbi.nlm.nih.gov/pubmed/23959445
http://dx.doi.org/10.1007/s10067-013-2351-y
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