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Rituximab as a front-line therapy for adult-onset minimal change disease with nephrotic syndrome
Minimal change disease (MCD) accounts for 15% of adult nephrotic syndrome (NS) cases. Adult-MCD patients may have more severe clinical features than pediatric patients. In children, Rituximab (RTX) has been used since 2006 to treat frequently relapsing NS. In adults, data about the efficacy of RTX f...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6034752/ https://www.ncbi.nlm.nih.gov/pubmed/29989000 http://dx.doi.org/10.18632/oncotarget.25612 |
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author | Fenoglio, Roberta Sciascia, Savino Beltrame, Giulietta Mesiano, Paola Ferro, Michela Quattrocchio, Giacomo Menegatti, Elisa Roccatello, Dario |
author_facet | Fenoglio, Roberta Sciascia, Savino Beltrame, Giulietta Mesiano, Paola Ferro, Michela Quattrocchio, Giacomo Menegatti, Elisa Roccatello, Dario |
author_sort | Fenoglio, Roberta |
collection | PubMed |
description | Minimal change disease (MCD) accounts for 15% of adult nephrotic syndrome (NS) cases. Adult-MCD patients may have more severe clinical features than pediatric patients. In children, Rituximab (RTX) has been used since 2006 to treat frequently relapsing NS. In adults, data about the efficacy of RTX for MCD are limited. We report our experience on the use of RTX in adult biopsy-proven MCD. Our series includes 6 adult patients (2 males and 4 females), age 45–73 years, treated with RTX (4 weekly doses of 375 mg/m(2)). Proteinuria decreased from 11,2 (23–4.8) g/24 hours to 0.6 (0–2) g/24 hours after 6 months, and to 0.4 (0–1, 4) g/24 h in the 4 pts with the longer follow-up. Creatinine decreased from 1.95 (0.5–5) mg/dl to 0.88 (0.6–1.3) mg/l. Five patients achieved a complete renal remission, while in 1 pt proteinuria decreased by 75%. RTX successfully depleted CD19 lymphocytes in 100% of pts for at least 6 months. No clinically relevant adverse events have been observed. This case series shows a remarkable efficacy of RTX in treatment of MCD. RTX can be an attractive alternative both in recurrent forms and in induction-therapy of MCD. RTX may be preferentially used in patients at a high risk of development of the adverse effects of corticosteroids and should be considered as an alternative option in patients with recurrent NS. Additional data are needed to inform clinical practice on how best to use RTX in this patient population, so that definitive randomized trials can be planned. |
format | Online Article Text |
id | pubmed-6034752 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-60347522018-07-09 Rituximab as a front-line therapy for adult-onset minimal change disease with nephrotic syndrome Fenoglio, Roberta Sciascia, Savino Beltrame, Giulietta Mesiano, Paola Ferro, Michela Quattrocchio, Giacomo Menegatti, Elisa Roccatello, Dario Oncotarget Research Paper: Immunology Minimal change disease (MCD) accounts for 15% of adult nephrotic syndrome (NS) cases. Adult-MCD patients may have more severe clinical features than pediatric patients. In children, Rituximab (RTX) has been used since 2006 to treat frequently relapsing NS. In adults, data about the efficacy of RTX for MCD are limited. We report our experience on the use of RTX in adult biopsy-proven MCD. Our series includes 6 adult patients (2 males and 4 females), age 45–73 years, treated with RTX (4 weekly doses of 375 mg/m(2)). Proteinuria decreased from 11,2 (23–4.8) g/24 hours to 0.6 (0–2) g/24 hours after 6 months, and to 0.4 (0–1, 4) g/24 h in the 4 pts with the longer follow-up. Creatinine decreased from 1.95 (0.5–5) mg/dl to 0.88 (0.6–1.3) mg/l. Five patients achieved a complete renal remission, while in 1 pt proteinuria decreased by 75%. RTX successfully depleted CD19 lymphocytes in 100% of pts for at least 6 months. No clinically relevant adverse events have been observed. This case series shows a remarkable efficacy of RTX in treatment of MCD. RTX can be an attractive alternative both in recurrent forms and in induction-therapy of MCD. RTX may be preferentially used in patients at a high risk of development of the adverse effects of corticosteroids and should be considered as an alternative option in patients with recurrent NS. Additional data are needed to inform clinical practice on how best to use RTX in this patient population, so that definitive randomized trials can be planned. Impact Journals LLC 2018-06-22 /pmc/articles/PMC6034752/ /pubmed/29989000 http://dx.doi.org/10.18632/oncotarget.25612 Text en Copyright: © 2018 Fenoglio et al. http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Research Paper: Immunology Fenoglio, Roberta Sciascia, Savino Beltrame, Giulietta Mesiano, Paola Ferro, Michela Quattrocchio, Giacomo Menegatti, Elisa Roccatello, Dario Rituximab as a front-line therapy for adult-onset minimal change disease with nephrotic syndrome |
title | Rituximab as a front-line therapy for adult-onset minimal change disease with nephrotic syndrome |
title_full | Rituximab as a front-line therapy for adult-onset minimal change disease with nephrotic syndrome |
title_fullStr | Rituximab as a front-line therapy for adult-onset minimal change disease with nephrotic syndrome |
title_full_unstemmed | Rituximab as a front-line therapy for adult-onset minimal change disease with nephrotic syndrome |
title_short | Rituximab as a front-line therapy for adult-onset minimal change disease with nephrotic syndrome |
title_sort | rituximab as a front-line therapy for adult-onset minimal change disease with nephrotic syndrome |
topic | Research Paper: Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6034752/ https://www.ncbi.nlm.nih.gov/pubmed/29989000 http://dx.doi.org/10.18632/oncotarget.25612 |
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