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Antibody-Guided Therapy in Phospholipase A2 Receptor-Associated Membranous Nephropathy
INTRODUCTION: A 6-month course of cyclophosphamide (CP) and steroids is effective in primary membranous nephropathy (MN), but unappealing because of long-term side effects. We evaluated efficacy of an “antibody-guided” treatment schedule. METHODS: Patients with phospholipase A2 receptor (PLA2R)-rela...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10014436/ https://www.ncbi.nlm.nih.gov/pubmed/36938074 http://dx.doi.org/10.1016/j.ekir.2022.12.003 |
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author | Vink, Coralien H. Logt, Anne-Els van de van der Molen, Renate G. Hofstra, Julia M. Wetzels, Jack F.M. |
author_facet | Vink, Coralien H. Logt, Anne-Els van de van der Molen, Renate G. Hofstra, Julia M. Wetzels, Jack F.M. |
author_sort | Vink, Coralien H. |
collection | PubMed |
description | INTRODUCTION: A 6-month course of cyclophosphamide (CP) and steroids is effective in primary membranous nephropathy (MN), but unappealing because of long-term side effects. We evaluated efficacy of an “antibody-guided” treatment schedule. METHODS: Patients with phospholipase A2 receptor (PLA2R)-related MN and high risk of progression were treated with CP 1.5 mg/kg/d and steroids in cycles of 8 weeks. Anti-PLA2R antibodies were measured by indirect immunofluorescence (IIFT) at 8, 16, and 24 weeks, and a negative test resulted in withdrawal of CP, and rapid tapering of prednisone. In patients with persistent anti-PLA2R antibodies at 24 weeks, CP was switched to mycophenolate mofetil. Treatment was repeated in patients with a relapse. RESULTS: Our analysis included 65 patients (48 males, 17 females), age 61 ± 12 years, estimated glomerular filtration rate (eGFR) 46 ml/min per 1.73 m(2) (35−68), urine protein-to-creatinine ratio 7.7 grams/10 mmol creatinine (5.4−11.1) and serum albumin 20 g/l (16−26). Immunologic remission rate was 71% after 8 weeks, 86% after 16 weeks, 88% after 24 weeks, and 94% after 3 years. Twenty-seven patients (42%) had persistent clinical remission after only 8 weeks of therapy. Sixteen patients needed a second course of therapy because of immunologic or clinical relapse. Follow-up was 37 (26−58) months. Overall partial remission rate was 92%. One patient developed end-stage kidney disease. Antibody-guided therapy (ABG) was as effective as the standard 6-month course, whereas providing a lower cumulative dose of CP (11.1 [8.0−18.5] vs. 18.9 [14.2−23.6] grams). CONCLUSION: ABG is effective, and allows individualized therapy, with many patients responding to 8 weeks of CP-based therapy. |
format | Online Article Text |
id | pubmed-10014436 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-100144362023-03-16 Antibody-Guided Therapy in Phospholipase A2 Receptor-Associated Membranous Nephropathy Vink, Coralien H. Logt, Anne-Els van de van der Molen, Renate G. Hofstra, Julia M. Wetzels, Jack F.M. Kidney Int Rep Clinical Research INTRODUCTION: A 6-month course of cyclophosphamide (CP) and steroids is effective in primary membranous nephropathy (MN), but unappealing because of long-term side effects. We evaluated efficacy of an “antibody-guided” treatment schedule. METHODS: Patients with phospholipase A2 receptor (PLA2R)-related MN and high risk of progression were treated with CP 1.5 mg/kg/d and steroids in cycles of 8 weeks. Anti-PLA2R antibodies were measured by indirect immunofluorescence (IIFT) at 8, 16, and 24 weeks, and a negative test resulted in withdrawal of CP, and rapid tapering of prednisone. In patients with persistent anti-PLA2R antibodies at 24 weeks, CP was switched to mycophenolate mofetil. Treatment was repeated in patients with a relapse. RESULTS: Our analysis included 65 patients (48 males, 17 females), age 61 ± 12 years, estimated glomerular filtration rate (eGFR) 46 ml/min per 1.73 m(2) (35−68), urine protein-to-creatinine ratio 7.7 grams/10 mmol creatinine (5.4−11.1) and serum albumin 20 g/l (16−26). Immunologic remission rate was 71% after 8 weeks, 86% after 16 weeks, 88% after 24 weeks, and 94% after 3 years. Twenty-seven patients (42%) had persistent clinical remission after only 8 weeks of therapy. Sixteen patients needed a second course of therapy because of immunologic or clinical relapse. Follow-up was 37 (26−58) months. Overall partial remission rate was 92%. One patient developed end-stage kidney disease. Antibody-guided therapy (ABG) was as effective as the standard 6-month course, whereas providing a lower cumulative dose of CP (11.1 [8.0−18.5] vs. 18.9 [14.2−23.6] grams). CONCLUSION: ABG is effective, and allows individualized therapy, with many patients responding to 8 weeks of CP-based therapy. Elsevier 2022-12-13 /pmc/articles/PMC10014436/ /pubmed/36938074 http://dx.doi.org/10.1016/j.ekir.2022.12.003 Text en © 2022 Published by Elsevier Inc. on behalf of the International Society of Nephrology. https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Clinical Research Vink, Coralien H. Logt, Anne-Els van de van der Molen, Renate G. Hofstra, Julia M. Wetzels, Jack F.M. Antibody-Guided Therapy in Phospholipase A2 Receptor-Associated Membranous Nephropathy |
title | Antibody-Guided Therapy in Phospholipase A2 Receptor-Associated Membranous Nephropathy |
title_full | Antibody-Guided Therapy in Phospholipase A2 Receptor-Associated Membranous Nephropathy |
title_fullStr | Antibody-Guided Therapy in Phospholipase A2 Receptor-Associated Membranous Nephropathy |
title_full_unstemmed | Antibody-Guided Therapy in Phospholipase A2 Receptor-Associated Membranous Nephropathy |
title_short | Antibody-Guided Therapy in Phospholipase A2 Receptor-Associated Membranous Nephropathy |
title_sort | antibody-guided therapy in phospholipase a2 receptor-associated membranous nephropathy |
topic | Clinical Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10014436/ https://www.ncbi.nlm.nih.gov/pubmed/36938074 http://dx.doi.org/10.1016/j.ekir.2022.12.003 |
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