Management of severe renal disease in anti-neutrophil-cytoplasmic-antibody-associated vasculitis: the place of rituximab and plasma exchange?

Abstract Objective The optimal induction therapy for severe glomerulonephritis of ANCA-associated vasculitis (AAV) is debated. We compared the efficacy of glucocorticoid and rituximab (RTX) or CYC induction therapy for severe AAV-related glomerulonephritis and evaluated the potential benefit of plas...

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Veröffentlicht in:Rheumatology 2022-10, Vol.61 (10), p.4056-4064
Hauptverfasser: Morel, Pauline, Karras, Alexandre, Porcher, Raphaël, Belenfant, Xavier, Audard, Vincent, Rafat, Cédric, Hanouna, Guillaume, Beaudreuil, Séverine, Vilain, Cédric, Hummel, Aurélie, Terrier, Benjamin, Pillebout, Evangeline, Groh, Matthieu, Jouenne, Romain, Dhote, Robin, Fain, Olivier, Ponsoye, Matthieu, Noel, Nicolas, Limal, Nicolas, Puéchal, Xavier, Le Jeunne, Claire, Guillevin, Loïc, Mouthon, Luc, Régent, Alexis
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container_end_page 4064
container_issue 10
container_start_page 4056
container_title Rheumatology
container_volume 61
creator Morel, Pauline
Karras, Alexandre
Porcher, Raphaël
Belenfant, Xavier
Audard, Vincent
Rafat, Cédric
Hanouna, Guillaume
Beaudreuil, Séverine
Vilain, Cédric
Hummel, Aurélie
Terrier, Benjamin
Pillebout, Evangeline
Groh, Matthieu
Jouenne, Romain
Dhote, Robin
Fain, Olivier
Ponsoye, Matthieu
Noel, Nicolas
Limal, Nicolas
Puéchal, Xavier
Le Jeunne, Claire
Guillevin, Loïc
Mouthon, Luc
Régent, Alexis
description Abstract Objective The optimal induction therapy for severe glomerulonephritis of ANCA-associated vasculitis (AAV) is debated. We compared the efficacy of glucocorticoid and rituximab (RTX) or CYC induction therapy for severe AAV-related glomerulonephritis and evaluated the potential benefit of plasma exchange (PE) as adjunct therapy to CYC. Methods This retrospective, multicentre study included AAV patients with severe renal active disease (serum creatinine level ≥350 µmol/l and/or estimated glomerular filtration ratio ≤15 ml/min/1.73 m2). Propensity-score analysis was used to adjust for potential confounders. Results Between 2005 and 2017, 153 patients with AAV-related glomerulonephritis were studied (96 [60%] men; mean [s.d.] age 63 [13.1] years): 19 (12%) were treated with RTX and 134 (88%) with CYC. Remission rates did not differ between RTX- and CYC-treated groups. Although more patients with RTX than CYC were dialysis-free at month (M) 12 (79% vs 68%), the difference was not significant after adjustment. Among 134 patients with CYC-treated glomerulonephritis, 76 (57%) also had PE. M3 and M6 remission rates were comparable for weighted CYC groups with or without PE. For weighted groups, the dialysis-free survival rate with CYC was higher with than without PE at M6 (72% vs 64%; odds ratio 2.58) and M12 (74% vs 60%; odds ratio 2.78) reaching statistical significance at M12. Conclusion We could not find any difference between RTX and CYC as induction therapy for patients with severe AAV-related glomerulonephritis. In patients receiving CYC induction regimen, the addition of PE conferred short-term benefits with higher dialysis-free rate at M12.
doi_str_mv 10.1093/rheumatology/keac046
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We compared the efficacy of glucocorticoid and rituximab (RTX) or CYC induction therapy for severe AAV-related glomerulonephritis and evaluated the potential benefit of plasma exchange (PE) as adjunct therapy to CYC. Methods This retrospective, multicentre study included AAV patients with severe renal active disease (serum creatinine level ≥350 µmol/l and/or estimated glomerular filtration ratio ≤15 ml/min/1.73 m2). Propensity-score analysis was used to adjust for potential confounders. Results Between 2005 and 2017, 153 patients with AAV-related glomerulonephritis were studied (96 [60%] men; mean [s.d.] age 63 [13.1] years): 19 (12%) were treated with RTX and 134 (88%) with CYC. Remission rates did not differ between RTX- and CYC-treated groups. Although more patients with RTX than CYC were dialysis-free at month (M) 12 (79% vs 68%), the difference was not significant after adjustment. Among 134 patients with CYC-treated glomerulonephritis, 76 (57%) also had PE. M3 and M6 remission rates were comparable for weighted CYC groups with or without PE. For weighted groups, the dialysis-free survival rate with CYC was higher with than without PE at M6 (72% vs 64%; odds ratio 2.58) and M12 (74% vs 60%; odds ratio 2.78) reaching statistical significance at M12. Conclusion We could not find any difference between RTX and CYC as induction therapy for patients with severe AAV-related glomerulonephritis. In patients receiving CYC induction regimen, the addition of PE conferred short-term benefits with higher dialysis-free rate at M12.</description><identifier>ISSN: 1462-0324</identifier><identifier>EISSN: 1462-0332</identifier><identifier>EISSN: 1460-2172</identifier><identifier>DOI: 10.1093/rheumatology/keac046</identifier><identifier>PMID: 35108368</identifier><language>eng</language><publisher>England: Oxford University Press</publisher><subject>Human health and pathology ; Life Sciences</subject><ispartof>Rheumatology, 2022-10, Vol.61 (10), p.4056-4064</ispartof><rights>The Author(s) 2022. Published by Oxford University Press on behalf of the British Society for Rheumatology. All rights reserved. For permissions, please email: journals.permissions@oup.com 2022</rights><rights>The Author(s) 2022. Published by Oxford University Press on behalf of the British Society for Rheumatology. All rights reserved. For permissions, please email: journals.permissions@oup.com.</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c381t-190232af5079fe802b769783054c61811abbd1d2f1ccc933ee3572b9be6a3d153</citedby><cites>FETCH-LOGICAL-c381t-190232af5079fe802b769783054c61811abbd1d2f1ccc933ee3572b9be6a3d153</cites><orcidid>0000-0003-3573-9203 ; 0000-0001-6463-2160 ; 0000-0002-5277-4679 ; 0000-0002-1974-3870 ; 0000-0002-9838-246X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,1583,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35108368$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-04249800$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Morel, Pauline</creatorcontrib><creatorcontrib>Karras, Alexandre</creatorcontrib><creatorcontrib>Porcher, Raphaël</creatorcontrib><creatorcontrib>Belenfant, Xavier</creatorcontrib><creatorcontrib>Audard, Vincent</creatorcontrib><creatorcontrib>Rafat, Cédric</creatorcontrib><creatorcontrib>Hanouna, Guillaume</creatorcontrib><creatorcontrib>Beaudreuil, Séverine</creatorcontrib><creatorcontrib>Vilain, Cédric</creatorcontrib><creatorcontrib>Hummel, Aurélie</creatorcontrib><creatorcontrib>Terrier, Benjamin</creatorcontrib><creatorcontrib>Pillebout, Evangeline</creatorcontrib><creatorcontrib>Groh, Matthieu</creatorcontrib><creatorcontrib>Jouenne, Romain</creatorcontrib><creatorcontrib>Dhote, Robin</creatorcontrib><creatorcontrib>Fain, Olivier</creatorcontrib><creatorcontrib>Ponsoye, Matthieu</creatorcontrib><creatorcontrib>Noel, Nicolas</creatorcontrib><creatorcontrib>Limal, Nicolas</creatorcontrib><creatorcontrib>Puéchal, Xavier</creatorcontrib><creatorcontrib>Le Jeunne, Claire</creatorcontrib><creatorcontrib>Guillevin, Loïc</creatorcontrib><creatorcontrib>Mouthon, Luc</creatorcontrib><creatorcontrib>Régent, Alexis</creatorcontrib><creatorcontrib>French Vasculitis Study Group (FSVG)</creatorcontrib><title>Management of severe renal disease in anti-neutrophil-cytoplasmic-antibody-associated vasculitis: the place of rituximab and plasma exchange?</title><title>Rheumatology</title><addtitle>Rheumatology (Oxford)</addtitle><description>Abstract Objective The optimal induction therapy for severe glomerulonephritis of ANCA-associated vasculitis (AAV) is debated. We compared the efficacy of glucocorticoid and rituximab (RTX) or CYC induction therapy for severe AAV-related glomerulonephritis and evaluated the potential benefit of plasma exchange (PE) as adjunct therapy to CYC. Methods This retrospective, multicentre study included AAV patients with severe renal active disease (serum creatinine level ≥350 µmol/l and/or estimated glomerular filtration ratio ≤15 ml/min/1.73 m2). Propensity-score analysis was used to adjust for potential confounders. Results Between 2005 and 2017, 153 patients with AAV-related glomerulonephritis were studied (96 [60%] men; mean [s.d.] age 63 [13.1] years): 19 (12%) were treated with RTX and 134 (88%) with CYC. Remission rates did not differ between RTX- and CYC-treated groups. Although more patients with RTX than CYC were dialysis-free at month (M) 12 (79% vs 68%), the difference was not significant after adjustment. Among 134 patients with CYC-treated glomerulonephritis, 76 (57%) also had PE. M3 and M6 remission rates were comparable for weighted CYC groups with or without PE. For weighted groups, the dialysis-free survival rate with CYC was higher with than without PE at M6 (72% vs 64%; odds ratio 2.58) and M12 (74% vs 60%; odds ratio 2.78) reaching statistical significance at M12. Conclusion We could not find any difference between RTX and CYC as induction therapy for patients with severe AAV-related glomerulonephritis. 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We compared the efficacy of glucocorticoid and rituximab (RTX) or CYC induction therapy for severe AAV-related glomerulonephritis and evaluated the potential benefit of plasma exchange (PE) as adjunct therapy to CYC. Methods This retrospective, multicentre study included AAV patients with severe renal active disease (serum creatinine level ≥350 µmol/l and/or estimated glomerular filtration ratio ≤15 ml/min/1.73 m2). Propensity-score analysis was used to adjust for potential confounders. Results Between 2005 and 2017, 153 patients with AAV-related glomerulonephritis were studied (96 [60%] men; mean [s.d.] age 63 [13.1] years): 19 (12%) were treated with RTX and 134 (88%) with CYC. Remission rates did not differ between RTX- and CYC-treated groups. Although more patients with RTX than CYC were dialysis-free at month (M) 12 (79% vs 68%), the difference was not significant after adjustment. Among 134 patients with CYC-treated glomerulonephritis, 76 (57%) also had PE. M3 and M6 remission rates were comparable for weighted CYC groups with or without PE. For weighted groups, the dialysis-free survival rate with CYC was higher with than without PE at M6 (72% vs 64%; odds ratio 2.58) and M12 (74% vs 60%; odds ratio 2.78) reaching statistical significance at M12. Conclusion We could not find any difference between RTX and CYC as induction therapy for patients with severe AAV-related glomerulonephritis. In patients receiving CYC induction regimen, the addition of PE conferred short-term benefits with higher dialysis-free rate at M12.</abstract><cop>England</cop><pub>Oxford University Press</pub><pmid>35108368</pmid><doi>10.1093/rheumatology/keac046</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0003-3573-9203</orcidid><orcidid>https://orcid.org/0000-0001-6463-2160</orcidid><orcidid>https://orcid.org/0000-0002-5277-4679</orcidid><orcidid>https://orcid.org/0000-0002-1974-3870</orcidid><orcidid>https://orcid.org/0000-0002-9838-246X</orcidid></addata></record>
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title Management of severe renal disease in anti-neutrophil-cytoplasmic-antibody-associated vasculitis: the place of rituximab and plasma exchange?
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