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The efficacy of rituximab in adult frequently relapsing minimal change disease

BACKGROUND: Corticosteroids are the basis of treatment for nephrotic syndrome due to minimal change disease (MCD), but 25% of patients have frequently relapsing nephrotic syndrome (FRNS) and 30% become steroid dependent. Prolonged use of conventional immunosuppressants causes significant toxicity. R...

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Autores principales: King, Catherine, Logan, Sarah, Smith, Stuart W., Hewins, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5469552/
https://www.ncbi.nlm.nih.gov/pubmed/28638601
http://dx.doi.org/10.1093/ckj/sfw100
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author King, Catherine
Logan, Sarah
Smith, Stuart W.
Hewins, Peter
author_facet King, Catherine
Logan, Sarah
Smith, Stuart W.
Hewins, Peter
author_sort King, Catherine
collection PubMed
description BACKGROUND: Corticosteroids are the basis of treatment for nephrotic syndrome due to minimal change disease (MCD), but 25% of patients have frequently relapsing nephrotic syndrome (FRNS) and 30% become steroid dependent. Prolonged use of conventional immunosuppressants causes significant toxicity. Rituximab (RTX) is now included in guidelines for childhood MCD. Evidence for use in adult MCD is limited. We describe a single-centre experience of RTX use in adult MCD. METHODS: Outcomes of all adult MCD patients treated with RTX for FRNS between 2008 and 2015 were retrospectively analysed. RESULTS: Thirteen patients received RTX; 11/13 had childhood-onset MCD. All had FRNS and 10 were steroid dependent. Eleven patients experienced one or more major treatment side effect from conventional therapy. At the time of RTX treatment, six patients were relapsing. All entered remission after RTX. The median length of follow-up after the first RTX treatment was 20 months (range 6–85). After RTX, the rate of relapse was reduced from 4 to 0.4/year (Wilcoxon signed rank P ≤ 0.05). Seven patients relapsed after RTX after a median of 10 months (range 1–11). All seven relapsing patients were successfully re-treated with RTX and none developed RTX-resistant nephrosis. The median number of courses of RTX per patient was 1 (range 1–5). The number of additional immunosuppressants, steroid dependency and antihypertensive agents were also reduced. At the last follow-up, two patients remained on low-dose steroids. No RTX-related adverse events were observed. CONCLUSION: RTX is safe and effective in adults with FRNS due to MCD. The median rate of relapse is significantly reduced following RTX treatment and additional immunosuppressant exposure is minimized.
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spelling pubmed-54695522017-06-21 The efficacy of rituximab in adult frequently relapsing minimal change disease King, Catherine Logan, Sarah Smith, Stuart W. Hewins, Peter Clin Kidney J B-Cell Depletion in Glomerulopathies BACKGROUND: Corticosteroids are the basis of treatment for nephrotic syndrome due to minimal change disease (MCD), but 25% of patients have frequently relapsing nephrotic syndrome (FRNS) and 30% become steroid dependent. Prolonged use of conventional immunosuppressants causes significant toxicity. Rituximab (RTX) is now included in guidelines for childhood MCD. Evidence for use in adult MCD is limited. We describe a single-centre experience of RTX use in adult MCD. METHODS: Outcomes of all adult MCD patients treated with RTX for FRNS between 2008 and 2015 were retrospectively analysed. RESULTS: Thirteen patients received RTX; 11/13 had childhood-onset MCD. All had FRNS and 10 were steroid dependent. Eleven patients experienced one or more major treatment side effect from conventional therapy. At the time of RTX treatment, six patients were relapsing. All entered remission after RTX. The median length of follow-up after the first RTX treatment was 20 months (range 6–85). After RTX, the rate of relapse was reduced from 4 to 0.4/year (Wilcoxon signed rank P ≤ 0.05). Seven patients relapsed after RTX after a median of 10 months (range 1–11). All seven relapsing patients were successfully re-treated with RTX and none developed RTX-resistant nephrosis. The median number of courses of RTX per patient was 1 (range 1–5). The number of additional immunosuppressants, steroid dependency and antihypertensive agents were also reduced. At the last follow-up, two patients remained on low-dose steroids. No RTX-related adverse events were observed. CONCLUSION: RTX is safe and effective in adults with FRNS due to MCD. The median rate of relapse is significantly reduced following RTX treatment and additional immunosuppressant exposure is minimized. Oxford University Press 2017-02 2016-10-24 /pmc/articles/PMC5469552/ /pubmed/28638601 http://dx.doi.org/10.1093/ckj/sfw100 Text en © The Author 2016. Published by Oxford University Press on behalf of ERA-EDTA. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle B-Cell Depletion in Glomerulopathies
King, Catherine
Logan, Sarah
Smith, Stuart W.
Hewins, Peter
The efficacy of rituximab in adult frequently relapsing minimal change disease
title The efficacy of rituximab in adult frequently relapsing minimal change disease
title_full The efficacy of rituximab in adult frequently relapsing minimal change disease
title_fullStr The efficacy of rituximab in adult frequently relapsing minimal change disease
title_full_unstemmed The efficacy of rituximab in adult frequently relapsing minimal change disease
title_short The efficacy of rituximab in adult frequently relapsing minimal change disease
title_sort efficacy of rituximab in adult frequently relapsing minimal change disease
topic B-Cell Depletion in Glomerulopathies
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5469552/
https://www.ncbi.nlm.nih.gov/pubmed/28638601
http://dx.doi.org/10.1093/ckj/sfw100
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