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Rituximab in Patients With Phospholipase A2 Receptor–Associated Membranous Nephropathy and Severe CKD
INTRODUCTION: Patients with phospholipase A2 receptor (PLA2R)–associated membranous nephropathy and stage 4 or 5 chronic kidney disease are at high risk of end-stage kidney disease. In recent years, rituximab (RTX) emerged as a safe and efficient treatment for patients with PLA2R-associated membrano...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7056852/ https://www.ncbi.nlm.nih.gov/pubmed/32154454 http://dx.doi.org/10.1016/j.ekir.2019.12.006 |
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author | Hanset, Nicolas Esteve, Emmanuel Plaisier, Emmanuelle Johanet, Catherine Michel, Pierre-Antoine Boffa, Jean-Jacques Fievet, Patrick Mesnard, Laurent Morelle, Johann Ronco, Pierre Dahan, Karine |
author_facet | Hanset, Nicolas Esteve, Emmanuel Plaisier, Emmanuelle Johanet, Catherine Michel, Pierre-Antoine Boffa, Jean-Jacques Fievet, Patrick Mesnard, Laurent Morelle, Johann Ronco, Pierre Dahan, Karine |
author_sort | Hanset, Nicolas |
collection | PubMed |
description | INTRODUCTION: Patients with phospholipase A2 receptor (PLA2R)–associated membranous nephropathy and stage 4 or 5 chronic kidney disease are at high risk of end-stage kidney disease. In recent years, rituximab (RTX) emerged as a safe and efficient treatment for patients with PLA2R-associated membranous nephropathy. Whether its use is also appropriate in patients with an estimated glomerular filtration rate <30 ml/min per 1.73 m(2) has not been investigated. METHODS: We retrospectively reviewed characteristics and outcome of 13 patients with PLA2R-associated membranous nephropathy and stage 4 or 5 chronic kidney disease who received a total of 14 consecutive RTX treatments from January 2012 to March 2018. The treatment regimen consisted of either 2 weekly infusions of 375 mg/m(2) or 2 RTX infusions of 1 g/d two weeks apart. When needed, the regimen was repeated to achieve immunological remission. RESULTS: The mean estimated glomerular filtration rate, serum albumin level, and urinary protein level at the first RTX infusion were 18 ± 7 ml/min per 1.73 m(2), 25.2 ± 5.4 g/l, and 13.2 ± 7.5 g/d, respectively, with all patients being tested positive for serum PLA2R antibodies. Ten treatment courses led to an increase in estimated glomerular filtration rate and remission of nephrotic syndrome after a median follow-up of 40.8 months (interquartile range, 14.8–46.8). Conversely, 4 RTX treatments were unsuccessful, with patients requiring chronic hemodialysis within 1 year. The urinary albumin-to-protein ratio before treatment was predictive of renal response. Immunological remission occurred after 11 treatment courses and was associated with clinical response in 10 of 11 patients. Three patients experienced severe adverse events. CONCLUSION: RTX seems effective and reasonably safe in PLA2R-associated membranous nephropathy with stage 4 or 5 chronic kidney disease. Immunological remission is associated with a good clinical outcome. |
format | Online Article Text |
id | pubmed-7056852 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-70568522020-03-09 Rituximab in Patients With Phospholipase A2 Receptor–Associated Membranous Nephropathy and Severe CKD Hanset, Nicolas Esteve, Emmanuel Plaisier, Emmanuelle Johanet, Catherine Michel, Pierre-Antoine Boffa, Jean-Jacques Fievet, Patrick Mesnard, Laurent Morelle, Johann Ronco, Pierre Dahan, Karine Kidney Int Rep Clinical Research INTRODUCTION: Patients with phospholipase A2 receptor (PLA2R)–associated membranous nephropathy and stage 4 or 5 chronic kidney disease are at high risk of end-stage kidney disease. In recent years, rituximab (RTX) emerged as a safe and efficient treatment for patients with PLA2R-associated membranous nephropathy. Whether its use is also appropriate in patients with an estimated glomerular filtration rate <30 ml/min per 1.73 m(2) has not been investigated. METHODS: We retrospectively reviewed characteristics and outcome of 13 patients with PLA2R-associated membranous nephropathy and stage 4 or 5 chronic kidney disease who received a total of 14 consecutive RTX treatments from January 2012 to March 2018. The treatment regimen consisted of either 2 weekly infusions of 375 mg/m(2) or 2 RTX infusions of 1 g/d two weeks apart. When needed, the regimen was repeated to achieve immunological remission. RESULTS: The mean estimated glomerular filtration rate, serum albumin level, and urinary protein level at the first RTX infusion were 18 ± 7 ml/min per 1.73 m(2), 25.2 ± 5.4 g/l, and 13.2 ± 7.5 g/d, respectively, with all patients being tested positive for serum PLA2R antibodies. Ten treatment courses led to an increase in estimated glomerular filtration rate and remission of nephrotic syndrome after a median follow-up of 40.8 months (interquartile range, 14.8–46.8). Conversely, 4 RTX treatments were unsuccessful, with patients requiring chronic hemodialysis within 1 year. The urinary albumin-to-protein ratio before treatment was predictive of renal response. Immunological remission occurred after 11 treatment courses and was associated with clinical response in 10 of 11 patients. Three patients experienced severe adverse events. CONCLUSION: RTX seems effective and reasonably safe in PLA2R-associated membranous nephropathy with stage 4 or 5 chronic kidney disease. Immunological remission is associated with a good clinical outcome. Elsevier 2019-12-20 /pmc/articles/PMC7056852/ /pubmed/32154454 http://dx.doi.org/10.1016/j.ekir.2019.12.006 Text en © 2019 International Society of Nephrology. Published by Elsevier Inc. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Clinical Research Hanset, Nicolas Esteve, Emmanuel Plaisier, Emmanuelle Johanet, Catherine Michel, Pierre-Antoine Boffa, Jean-Jacques Fievet, Patrick Mesnard, Laurent Morelle, Johann Ronco, Pierre Dahan, Karine Rituximab in Patients With Phospholipase A2 Receptor–Associated Membranous Nephropathy and Severe CKD |
title | Rituximab in Patients With Phospholipase A2 Receptor–Associated Membranous Nephropathy and Severe CKD |
title_full | Rituximab in Patients With Phospholipase A2 Receptor–Associated Membranous Nephropathy and Severe CKD |
title_fullStr | Rituximab in Patients With Phospholipase A2 Receptor–Associated Membranous Nephropathy and Severe CKD |
title_full_unstemmed | Rituximab in Patients With Phospholipase A2 Receptor–Associated Membranous Nephropathy and Severe CKD |
title_short | Rituximab in Patients With Phospholipase A2 Receptor–Associated Membranous Nephropathy and Severe CKD |
title_sort | rituximab in patients with phospholipase a2 receptor–associated membranous nephropathy and severe ckd |
topic | Clinical Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7056852/ https://www.ncbi.nlm.nih.gov/pubmed/32154454 http://dx.doi.org/10.1016/j.ekir.2019.12.006 |
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