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Immunosuppression for progressive membranous nephropathy: a UK randomised controlled trial

BACKGROUND: Membranous nephropathy leads to end-stage renal disease in more than 20% of patients. Although immunosuppressive therapy benefits some patients, trial evidence for the subset of patients with declining renal function is not available. We aimed to assess whether immunosuppression preserve...

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Autores principales: Howman, Andrew, Chapman, Tracey L, Langdon, Maria M, Ferguson, Caroline, Adu, Dwomoa, Feehally, John, Gaskin, Gillian J, Jayne, David RW, O'Donoghue, Donal, Boulton-Jones, Michael, Mathieson, Peter W
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lancet Publishing Group 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3590447/
https://www.ncbi.nlm.nih.gov/pubmed/23312808
http://dx.doi.org/10.1016/S0140-6736(12)61566-9
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author Howman, Andrew
Chapman, Tracey L
Langdon, Maria M
Ferguson, Caroline
Adu, Dwomoa
Feehally, John
Gaskin, Gillian J
Jayne, David RW
O'Donoghue, Donal
Boulton-Jones, Michael
Mathieson, Peter W
author_facet Howman, Andrew
Chapman, Tracey L
Langdon, Maria M
Ferguson, Caroline
Adu, Dwomoa
Feehally, John
Gaskin, Gillian J
Jayne, David RW
O'Donoghue, Donal
Boulton-Jones, Michael
Mathieson, Peter W
author_sort Howman, Andrew
collection PubMed
description BACKGROUND: Membranous nephropathy leads to end-stage renal disease in more than 20% of patients. Although immunosuppressive therapy benefits some patients, trial evidence for the subset of patients with declining renal function is not available. We aimed to assess whether immunosuppression preserves renal function in patients with idiopathic membranous nephropathy with declining renal function. METHODS: This randomised controlled trial was undertaken in 37 renal units across the UK. We recruited patients (18–75 years) with biopsy-proven idiopathic membranous nephropathy, a plasma creatinine concentration of less than 300 μmol/L, and at least a 20% decline in excretory renal function measured in the 2 years before study entry, based on at least three measurements over a period of 3 months or longer. Patients were randomly assigned (1:1:1) by a random number table to receive supportive treatment only, supportive treatment plus 6 months of alternating cycles of prednisolone and chlorambucil, or supportive treatment plus 12 months of ciclosporin. The primary outcome was a further 20% decline in renal function from baseline, analysed by intention to treat. The trial is registered as an International Standard Randomised Controlled Trial, number 99959692. FINDINGS: We randomly assigned 108 patients, 33 of whom received prednisolone and chlorambucil, 37 ciclosporin, and 38 supportive therapy alone. Two patients (one who received ciclosporin and one who received supportive therapy) were ineligible, so were not included in the intention-to-treat analysis, and 45 patients deviated from protocol before study end, mostly as a result of minor dose adjustments. Follow up was until primary endpoint or for minimum of 3 years if primary endpoint was not reached. Risk of further 20% decline in renal function was significantly lower in the prednisolone and chlorambucil group than in the supportive care group (19 [58%] of 33 patients reached endpoint vs 31 [84%] of 37, hazard ratio [HR] 0·44 [95% CI 0·24–0·78]; p=0·0042); risk did not differ between the ciclosporin (29 [81%] of 36) and supportive treatment only groups (HR 1·17 [0·70–1·95]; p=0·54), but did differ significantly across all three groups (p=0·003). Serious adverse events were frequent in all three groups but were higher in the prednisolone and chlorambucil group than in the supportive care only group (56 events vs 24 events; p=0·048). INTERPRETATION: For the subset of patients with idiopathic membranous nephropathy and deteriorating excretory renal function, 6 months' therapy with prednisolone and chlorambucil is the treatment approach best supported by our evidence. Ciclosporin should be avoided in this subset. FUNDING: Medical Research Council, Novartis, Renal Association, Kidney Research UK.
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spelling pubmed-35904472013-03-07 Immunosuppression for progressive membranous nephropathy: a UK randomised controlled trial Howman, Andrew Chapman, Tracey L Langdon, Maria M Ferguson, Caroline Adu, Dwomoa Feehally, John Gaskin, Gillian J Jayne, David RW O'Donoghue, Donal Boulton-Jones, Michael Mathieson, Peter W Lancet Articles BACKGROUND: Membranous nephropathy leads to end-stage renal disease in more than 20% of patients. Although immunosuppressive therapy benefits some patients, trial evidence for the subset of patients with declining renal function is not available. We aimed to assess whether immunosuppression preserves renal function in patients with idiopathic membranous nephropathy with declining renal function. METHODS: This randomised controlled trial was undertaken in 37 renal units across the UK. We recruited patients (18–75 years) with biopsy-proven idiopathic membranous nephropathy, a plasma creatinine concentration of less than 300 μmol/L, and at least a 20% decline in excretory renal function measured in the 2 years before study entry, based on at least three measurements over a period of 3 months or longer. Patients were randomly assigned (1:1:1) by a random number table to receive supportive treatment only, supportive treatment plus 6 months of alternating cycles of prednisolone and chlorambucil, or supportive treatment plus 12 months of ciclosporin. The primary outcome was a further 20% decline in renal function from baseline, analysed by intention to treat. The trial is registered as an International Standard Randomised Controlled Trial, number 99959692. FINDINGS: We randomly assigned 108 patients, 33 of whom received prednisolone and chlorambucil, 37 ciclosporin, and 38 supportive therapy alone. Two patients (one who received ciclosporin and one who received supportive therapy) were ineligible, so were not included in the intention-to-treat analysis, and 45 patients deviated from protocol before study end, mostly as a result of minor dose adjustments. Follow up was until primary endpoint or for minimum of 3 years if primary endpoint was not reached. Risk of further 20% decline in renal function was significantly lower in the prednisolone and chlorambucil group than in the supportive care group (19 [58%] of 33 patients reached endpoint vs 31 [84%] of 37, hazard ratio [HR] 0·44 [95% CI 0·24–0·78]; p=0·0042); risk did not differ between the ciclosporin (29 [81%] of 36) and supportive treatment only groups (HR 1·17 [0·70–1·95]; p=0·54), but did differ significantly across all three groups (p=0·003). Serious adverse events were frequent in all three groups but were higher in the prednisolone and chlorambucil group than in the supportive care only group (56 events vs 24 events; p=0·048). INTERPRETATION: For the subset of patients with idiopathic membranous nephropathy and deteriorating excretory renal function, 6 months' therapy with prednisolone and chlorambucil is the treatment approach best supported by our evidence. Ciclosporin should be avoided in this subset. FUNDING: Medical Research Council, Novartis, Renal Association, Kidney Research UK. Lancet Publishing Group 2013-03-02 /pmc/articles/PMC3590447/ /pubmed/23312808 http://dx.doi.org/10.1016/S0140-6736(12)61566-9 Text en © 2013 Elsevier Ltd. All rights reserved. This document may be redistributed and reused, subject to certain conditions (http://www.elsevier.com/wps/find/authorsview.authors/supplementalterms1.0) .
spellingShingle Articles
Howman, Andrew
Chapman, Tracey L
Langdon, Maria M
Ferguson, Caroline
Adu, Dwomoa
Feehally, John
Gaskin, Gillian J
Jayne, David RW
O'Donoghue, Donal
Boulton-Jones, Michael
Mathieson, Peter W
Immunosuppression for progressive membranous nephropathy: a UK randomised controlled trial
title Immunosuppression for progressive membranous nephropathy: a UK randomised controlled trial
title_full Immunosuppression for progressive membranous nephropathy: a UK randomised controlled trial
title_fullStr Immunosuppression for progressive membranous nephropathy: a UK randomised controlled trial
title_full_unstemmed Immunosuppression for progressive membranous nephropathy: a UK randomised controlled trial
title_short Immunosuppression for progressive membranous nephropathy: a UK randomised controlled trial
title_sort immunosuppression for progressive membranous nephropathy: a uk randomised controlled trial
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3590447/
https://www.ncbi.nlm.nih.gov/pubmed/23312808
http://dx.doi.org/10.1016/S0140-6736(12)61566-9
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