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Efficacy and safety of rituximab in the treatment of connective tissue disease-related interstitial lung disease

Interstitial lung disease (ILD) represents a severe pulmonary complication of connective tissue diseases, rheumatoid arthritis (RA), and antineutrophil cytoplasmic antibody-associated vasculitis. Treatment of ILD, mainly based on immunosuppression, remains challenging. Rituximab (RTX), a monoclonal...

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Autores principales: Vacchi, Caterina, Manfredi, Andreina, Cassone, Giulia, Erre, Gian Luca, Salvarani, Carlo, Sebastiani, Marco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioExcel Publishing Ltd 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7813433/
https://www.ncbi.nlm.nih.gov/pubmed/33505478
http://dx.doi.org/10.7573/dic.2020-8-7
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author Vacchi, Caterina
Manfredi, Andreina
Cassone, Giulia
Erre, Gian Luca
Salvarani, Carlo
Sebastiani, Marco
author_facet Vacchi, Caterina
Manfredi, Andreina
Cassone, Giulia
Erre, Gian Luca
Salvarani, Carlo
Sebastiani, Marco
author_sort Vacchi, Caterina
collection PubMed
description Interstitial lung disease (ILD) represents a severe pulmonary complication of connective tissue diseases, rheumatoid arthritis (RA), and antineutrophil cytoplasmic antibody-associated vasculitis. Treatment of ILD, mainly based on immunosuppression, remains challenging. Rituximab (RTX), a monoclonal antibody binding to CD20, is considered a valuable therapeutic choice in cases of refractory ILD. Here, we review the available efficacy and safety data on the use of RTX in the treatment of rheumatic disease-related ILD. Despite controversial efficacy data, RTX seems to be able to stabilize or improve ILD related to RA and antisynthetase syndrome and in established and severe ILD complicating systemic sclerosis. Fewer data are available regarding ILD related to Sjögren syndrome, systemic lupus erythematosus, and antineutrophil cytoplasmic antibody-associated vasculitis. To date, few prospective studies are available and randomized trials are still ongoing with the purpose of exploring the role of RTX in this condition, including the supposed relationship between efficacy and ILD radiologic patterns and safety data, up to now derived mainly from RA studies. Despite an overall acceptable safety profile, concerns remain regarding an increased infectious disease risk in patients with ILD as well as possible lung toxicity and the increased rate of immune-mediated reactions in patients with connective tissue diseases. In conclusion, RTX is a relevant therapeutic option for rheumatic disease-related ILD despite the existing uncertainties; ongoing trials are expected to clarify its use.
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spelling pubmed-78134332021-01-26 Efficacy and safety of rituximab in the treatment of connective tissue disease-related interstitial lung disease Vacchi, Caterina Manfredi, Andreina Cassone, Giulia Erre, Gian Luca Salvarani, Carlo Sebastiani, Marco Drugs Context Review Interstitial lung disease (ILD) represents a severe pulmonary complication of connective tissue diseases, rheumatoid arthritis (RA), and antineutrophil cytoplasmic antibody-associated vasculitis. Treatment of ILD, mainly based on immunosuppression, remains challenging. Rituximab (RTX), a monoclonal antibody binding to CD20, is considered a valuable therapeutic choice in cases of refractory ILD. Here, we review the available efficacy and safety data on the use of RTX in the treatment of rheumatic disease-related ILD. Despite controversial efficacy data, RTX seems to be able to stabilize or improve ILD related to RA and antisynthetase syndrome and in established and severe ILD complicating systemic sclerosis. Fewer data are available regarding ILD related to Sjögren syndrome, systemic lupus erythematosus, and antineutrophil cytoplasmic antibody-associated vasculitis. To date, few prospective studies are available and randomized trials are still ongoing with the purpose of exploring the role of RTX in this condition, including the supposed relationship between efficacy and ILD radiologic patterns and safety data, up to now derived mainly from RA studies. Despite an overall acceptable safety profile, concerns remain regarding an increased infectious disease risk in patients with ILD as well as possible lung toxicity and the increased rate of immune-mediated reactions in patients with connective tissue diseases. In conclusion, RTX is a relevant therapeutic option for rheumatic disease-related ILD despite the existing uncertainties; ongoing trials are expected to clarify its use. BioExcel Publishing Ltd 2021-01-15 /pmc/articles/PMC7813433/ /pubmed/33505478 http://dx.doi.org/10.7573/dic.2020-8-7 Text en Copyright © 2021 Vacchi C, Manfredi A, Cassone G, Erre GL, Salvarani C, Sebastiani M Published by Drugs in Context under Creative Commons License Deed CC BY NC ND 4.0 which allows anyone to copy, distribute, and transmit the article provided it is properly attributed in the manner specified below. No commercial use without permission.
spellingShingle Review
Vacchi, Caterina
Manfredi, Andreina
Cassone, Giulia
Erre, Gian Luca
Salvarani, Carlo
Sebastiani, Marco
Efficacy and safety of rituximab in the treatment of connective tissue disease-related interstitial lung disease
title Efficacy and safety of rituximab in the treatment of connective tissue disease-related interstitial lung disease
title_full Efficacy and safety of rituximab in the treatment of connective tissue disease-related interstitial lung disease
title_fullStr Efficacy and safety of rituximab in the treatment of connective tissue disease-related interstitial lung disease
title_full_unstemmed Efficacy and safety of rituximab in the treatment of connective tissue disease-related interstitial lung disease
title_short Efficacy and safety of rituximab in the treatment of connective tissue disease-related interstitial lung disease
title_sort efficacy and safety of rituximab in the treatment of connective tissue disease-related interstitial lung disease
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7813433/
https://www.ncbi.nlm.nih.gov/pubmed/33505478
http://dx.doi.org/10.7573/dic.2020-8-7
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