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C5a receptor inhibitor avacopan in immunoglobulin A nephropathy—an open-label pilot study

BACKGROUND: Improvement of proteinuria as a marker for disease activity is associated with a better renal outcome in immunoglobulin A nephropathy (IgAN). Complement is an effector pathway in IgA-mediated kidney injury. Avacopan, a selective C5a receptor inhibitor, has previously shown efficacy in an...

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Autores principales: Bruchfeld, Annette, Magin, Hasan, Nachman, Patrick, Parikh, Samir, Lafayette, Richard, Potarca, Antonia, Miao, Shichang, Bekker, Pirow
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9050557/
https://www.ncbi.nlm.nih.gov/pubmed/35498891
http://dx.doi.org/10.1093/ckj/sfab294
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author Bruchfeld, Annette
Magin, Hasan
Nachman, Patrick
Parikh, Samir
Lafayette, Richard
Potarca, Antonia
Miao, Shichang
Bekker, Pirow
author_facet Bruchfeld, Annette
Magin, Hasan
Nachman, Patrick
Parikh, Samir
Lafayette, Richard
Potarca, Antonia
Miao, Shichang
Bekker, Pirow
author_sort Bruchfeld, Annette
collection PubMed
description BACKGROUND: Improvement of proteinuria as a marker for disease activity is associated with a better renal outcome in immunoglobulin A nephropathy (IgAN). Complement is an effector pathway in IgA-mediated kidney injury. Avacopan, a selective C5a receptor inhibitor, has previously shown efficacy in anti-neutrophil cytoplasmic antibody–associated vasculitis. The aim of this study was to evaluate the safety and efficacy of avacopan in patients with IgAN with persistent proteinuria despite a maximally tolerated dose of renin–angiotensin–aldosterone system blockade. The efficacy evaluation was based on the change in proteinuria. METHODS: This open-label pilot trial enrolled adult patients with biopsy-proven IgAN, urinary protein:creatinine ratio (UPCR) >1 g/g creatinine and an estimated glomerular filtration rate (eGFR) >60 mL/min/1.73 m(2) or >45 mL/min/1.73 m(2) if eGFR has not declined >10 mL/min/1.73 m(2) over the previous 24 weeks. If the UPCR remained at >1 g/g creatinine after an 8-week run-in period, patients started avacopan 30 mg twice daily. The primary efficacy endpoint was the change in the slope of the UPCR from the 8-week run-in period to the slope in the 12-week avacopan dosing period. RESULTS: A total of 10 of 15 screened patients entered the run-in period. Seven patients with a UPCR >1 g/g creatinine received avacopan. Six of seven patients had numerical improvement in the UPCR during the avacopan treatment period, three of whom had a numerical improvement of ∼50% at week 12. At week 24, five of seven patients still showed numerical improvement in the UPCR compared with baseline. The urinary monocyte chemoattractant protein-1:creatinine ratio decreased numerically 30% by week 8, possibly reflecting the anti-inflammatory activity of avacopan. Avacopan was well tolerated. There was one serious adverse event of unstable angina, which was deemed to be unrelated to avacopan. CONCLUSIONS: This short-term pilot study showed an improvement in the slope of the UPCR, with ∼50% improvement in three of seven patients with IgAN. Longer avacopan treatment duration may be indicated for maximal benefit.
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spelling pubmed-90505572022-04-29 C5a receptor inhibitor avacopan in immunoglobulin A nephropathy—an open-label pilot study Bruchfeld, Annette Magin, Hasan Nachman, Patrick Parikh, Samir Lafayette, Richard Potarca, Antonia Miao, Shichang Bekker, Pirow Clin Kidney J Original Article BACKGROUND: Improvement of proteinuria as a marker for disease activity is associated with a better renal outcome in immunoglobulin A nephropathy (IgAN). Complement is an effector pathway in IgA-mediated kidney injury. Avacopan, a selective C5a receptor inhibitor, has previously shown efficacy in anti-neutrophil cytoplasmic antibody–associated vasculitis. The aim of this study was to evaluate the safety and efficacy of avacopan in patients with IgAN with persistent proteinuria despite a maximally tolerated dose of renin–angiotensin–aldosterone system blockade. The efficacy evaluation was based on the change in proteinuria. METHODS: This open-label pilot trial enrolled adult patients with biopsy-proven IgAN, urinary protein:creatinine ratio (UPCR) >1 g/g creatinine and an estimated glomerular filtration rate (eGFR) >60 mL/min/1.73 m(2) or >45 mL/min/1.73 m(2) if eGFR has not declined >10 mL/min/1.73 m(2) over the previous 24 weeks. If the UPCR remained at >1 g/g creatinine after an 8-week run-in period, patients started avacopan 30 mg twice daily. The primary efficacy endpoint was the change in the slope of the UPCR from the 8-week run-in period to the slope in the 12-week avacopan dosing period. RESULTS: A total of 10 of 15 screened patients entered the run-in period. Seven patients with a UPCR >1 g/g creatinine received avacopan. Six of seven patients had numerical improvement in the UPCR during the avacopan treatment period, three of whom had a numerical improvement of ∼50% at week 12. At week 24, five of seven patients still showed numerical improvement in the UPCR compared with baseline. The urinary monocyte chemoattractant protein-1:creatinine ratio decreased numerically 30% by week 8, possibly reflecting the anti-inflammatory activity of avacopan. Avacopan was well tolerated. There was one serious adverse event of unstable angina, which was deemed to be unrelated to avacopan. CONCLUSIONS: This short-term pilot study showed an improvement in the slope of the UPCR, with ∼50% improvement in three of seven patients with IgAN. Longer avacopan treatment duration may be indicated for maximal benefit. Oxford University Press 2022-01-24 /pmc/articles/PMC9050557/ /pubmed/35498891 http://dx.doi.org/10.1093/ckj/sfab294 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of the ERA. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://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 Original Article
Bruchfeld, Annette
Magin, Hasan
Nachman, Patrick
Parikh, Samir
Lafayette, Richard
Potarca, Antonia
Miao, Shichang
Bekker, Pirow
C5a receptor inhibitor avacopan in immunoglobulin A nephropathy—an open-label pilot study
title C5a receptor inhibitor avacopan in immunoglobulin A nephropathy—an open-label pilot study
title_full C5a receptor inhibitor avacopan in immunoglobulin A nephropathy—an open-label pilot study
title_fullStr C5a receptor inhibitor avacopan in immunoglobulin A nephropathy—an open-label pilot study
title_full_unstemmed C5a receptor inhibitor avacopan in immunoglobulin A nephropathy—an open-label pilot study
title_short C5a receptor inhibitor avacopan in immunoglobulin A nephropathy—an open-label pilot study
title_sort c5a receptor inhibitor avacopan in immunoglobulin a nephropathy—an open-label pilot study
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9050557/
https://www.ncbi.nlm.nih.gov/pubmed/35498891
http://dx.doi.org/10.1093/ckj/sfab294
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