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Rituximab for Steroid-Dependent Minimal Change Disease in Adults: Is It Time for a Change?

Minimal change disease (MCD) is a common cause of nephrotic syndrome, and steroid treatment is usually effective at the expense of adverse effects and frequent relapses. Rituximab, a monoclonal antibody against cluster of differentiation (CD)20 B-lymphocytes, leads to depletion of B-cells and has be...

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Autor principal: Kannan, Lakshmi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8933270/
https://www.ncbi.nlm.nih.gov/pubmed/35350528
http://dx.doi.org/10.7759/cureus.22313
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author Kannan, Lakshmi
author_facet Kannan, Lakshmi
author_sort Kannan, Lakshmi
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description Minimal change disease (MCD) is a common cause of nephrotic syndrome, and steroid treatment is usually effective at the expense of adverse effects and frequent relapses. Rituximab, a monoclonal antibody against cluster of differentiation (CD)20 B-lymphocytes, leads to depletion of B-cells and has been frequently used to treat relapsing MCD in children. The efficacy of rituximab in treating adult MCD is limited. We report our experience with the use of rituximab for adult biopsy-proven MCD. Our series includes four adult patients (two males and two females), aged 22-80 years, treated with rituximab. All four patients achieved a complete remission with rituximab which lasted from 12 to 19 months. No adverse events from rituximab were observed. This shows the remarkable efficacy of rituximab in the treatment of minimal change disease in adults and may be preferred in patients at high risk for the development of adverse events from corticosteroids.
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spelling pubmed-89332702022-03-28 Rituximab for Steroid-Dependent Minimal Change Disease in Adults: Is It Time for a Change? Kannan, Lakshmi Cureus Pathology Minimal change disease (MCD) is a common cause of nephrotic syndrome, and steroid treatment is usually effective at the expense of adverse effects and frequent relapses. Rituximab, a monoclonal antibody against cluster of differentiation (CD)20 B-lymphocytes, leads to depletion of B-cells and has been frequently used to treat relapsing MCD in children. The efficacy of rituximab in treating adult MCD is limited. We report our experience with the use of rituximab for adult biopsy-proven MCD. Our series includes four adult patients (two males and two females), aged 22-80 years, treated with rituximab. All four patients achieved a complete remission with rituximab which lasted from 12 to 19 months. No adverse events from rituximab were observed. This shows the remarkable efficacy of rituximab in the treatment of minimal change disease in adults and may be preferred in patients at high risk for the development of adverse events from corticosteroids. Cureus 2022-02-17 /pmc/articles/PMC8933270/ /pubmed/35350528 http://dx.doi.org/10.7759/cureus.22313 Text en Copyright © 2022, Kannan et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Pathology
Kannan, Lakshmi
Rituximab for Steroid-Dependent Minimal Change Disease in Adults: Is It Time for a Change?
title Rituximab for Steroid-Dependent Minimal Change Disease in Adults: Is It Time for a Change?
title_full Rituximab for Steroid-Dependent Minimal Change Disease in Adults: Is It Time for a Change?
title_fullStr Rituximab for Steroid-Dependent Minimal Change Disease in Adults: Is It Time for a Change?
title_full_unstemmed Rituximab for Steroid-Dependent Minimal Change Disease in Adults: Is It Time for a Change?
title_short Rituximab for Steroid-Dependent Minimal Change Disease in Adults: Is It Time for a Change?
title_sort rituximab for steroid-dependent minimal change disease in adults: is it time for a change?
topic Pathology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8933270/
https://www.ncbi.nlm.nih.gov/pubmed/35350528
http://dx.doi.org/10.7759/cureus.22313
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