Multicentric study comparing cyclosporine, mycophenolate mofetil and azathioprine in the maintenance therapy of lupus nephritis: 8 years follow up.


Journal

Journal of nephrology
ISSN: 1724-6059
Titre abrégé: J Nephrol
Pays: Italy
ID NLM: 9012268

Informations de publication

Date de publication:
04 2021
Historique:
received: 09 03 2020
accepted: 11 05 2020
pubmed: 29 5 2020
medline: 19 8 2021
entrez: 29 5 2020
Statut: ppublish

Résumé

The ideal long-term maintenance therapy of Lupus Nephritis (LN) is still a matter of debate. The present study was aimed at comparing the efficacy/safety profile of cyclosporine (CsA), mycophenolate mofetil (MMF) and azathioprine (AZA) in long-term maintenance therapy of LN. We performed a retrospective study of patients with biopsy-proven active LN. After induction therapy, all patients received maintenance therapy with CsA, MMF or AZA based on medical decision. Primary endpoint was complete renal remission (CRR) after 8 years (defined as proteinuria < 0.5 g/24 h, eGFR > 60 ml/min/1.73 mq); secondary endpoints were: CRR after 1 year, renal and extrarenal flares, progression of chronic kidney disease (CKD stage 3 or above) and side-effects. Out of 106 patients, 34 received CsA, 36 MMF and 36 AZA. Clinical and histological characteristics at start of induction therapy were comparable among groups. At start of maintenance therapy, CsA patients had significantly higher proteinuria (P = 0.004) or nephrotic syndrome (P = 0.024) and significantly lower CRR (23.5% vs 55.5% on MMF and 41.7% on AZA, P = 0.024). At one year, CRR was similar in the three groups (79.4% on CsA, 63.8% on MMF, 58.3% on AZA, P = 0.2). At 8 years, the primary endpoint was achieved by 79.4% of CsA vs 83.3% of MMF and 77.8% of AZA patients (P = 0.83); 24 h proteinuria, serum creatinine, eGFR were similar. CKD stage 3 or above developed in 8.8% of CsA, in 8.3% of MMF and in 8.3% of AZA patients (P = 0.92). Flares-free survival curves and incidence of side-effects were not different. This is the first study comparing CsA, MMF and AZA on long-term LN maintenance therapy. All treatments had similar efficacy in achieving and maintaining CRR, despite more severe baseline clinical features in patients treated with CsA.

Sections du résumé

BACKGROUND
The ideal long-term maintenance therapy of Lupus Nephritis (LN) is still a matter of debate. The present study was aimed at comparing the efficacy/safety profile of cyclosporine (CsA), mycophenolate mofetil (MMF) and azathioprine (AZA) in long-term maintenance therapy of LN.
METHODS
We performed a retrospective study of patients with biopsy-proven active LN. After induction therapy, all patients received maintenance therapy with CsA, MMF or AZA based on medical decision. Primary endpoint was complete renal remission (CRR) after 8 years (defined as proteinuria < 0.5 g/24 h, eGFR > 60 ml/min/1.73 mq); secondary endpoints were: CRR after 1 year, renal and extrarenal flares, progression of chronic kidney disease (CKD stage 3 or above) and side-effects.
RESULTS
Out of 106 patients, 34 received CsA, 36 MMF and 36 AZA. Clinical and histological characteristics at start of induction therapy were comparable among groups. At start of maintenance therapy, CsA patients had significantly higher proteinuria (P = 0.004) or nephrotic syndrome (P = 0.024) and significantly lower CRR (23.5% vs 55.5% on MMF and 41.7% on AZA, P = 0.024). At one year, CRR was similar in the three groups (79.4% on CsA, 63.8% on MMF, 58.3% on AZA, P = 0.2). At 8 years, the primary endpoint was achieved by 79.4% of CsA vs 83.3% of MMF and 77.8% of AZA patients (P = 0.83); 24 h proteinuria, serum creatinine, eGFR were similar. CKD stage 3 or above developed in 8.8% of CsA, in 8.3% of MMF and in 8.3% of AZA patients (P = 0.92). Flares-free survival curves and incidence of side-effects were not different.
CONCLUSIONS
This is the first study comparing CsA, MMF and AZA on long-term LN maintenance therapy. All treatments had similar efficacy in achieving and maintaining CRR, despite more severe baseline clinical features in patients treated with CsA.

Identifiants

pubmed: 32462476
doi: 10.1007/s40620-020-00753-w
pii: 10.1007/s40620-020-00753-w
doi:

Substances chimiques

Immunosuppressive Agents 0
Cyclosporine 83HN0GTJ6D
Mycophenolic Acid HU9DX48N0T
Azathioprine MRK240IY2L

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

389-398

Références

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Auteurs

Lorenza Maria Argolini (LM)

Division of Clinical Rheumatology, ASST Istituto Gaetano Pini - CTO, Milan, Italy.

Giulia Frontini (G)

Divisione di Nefrologia e Dialisi-Padiglione Croff, Fondazione Ca' Granda IRCCS Ospedale Maggiore Policlinico Milano, Via della Commenda 15, 20122, Milano, Italy.

Elena Elefante (E)

Department of Clinical and Experimental Medicine, Rheumatology Unit, University of Pisa, Pisa, Italy.

Francesca Saccon (F)

Division of Rheumatology, Department of Medicine, DIMED, University of Padua, Padua, Italy.

Valentina Binda (V)

Divisione di Nefrologia e Dialisi-Padiglione Croff, Fondazione Ca' Granda IRCCS Ospedale Maggiore Policlinico Milano, Via della Commenda 15, 20122, Milano, Italy.

Chiara Tani (C)

Department of Clinical and Experimental Medicine, Rheumatology Unit, University of Pisa, Pisa, Italy.

Isabella Scotti (I)

Division of Clinical Rheumatology, ASST Istituto Gaetano Pini - CTO, Milan, Italy.
Department of Clinical Sciences and Community Health, University of Milan, ASST Istituto Gaetano Pini - CTO, Milan, Italy.

Linda Carli (L)

Department of Clinical and Experimental Medicine, Rheumatology Unit, University of Pisa, Pisa, Italy.

Mariele Gatto (M)

Division of Rheumatology, Department of Medicine, DIMED, University of Padua, Padua, Italy.

Ciro Esposito (C)

Unit of Nephrology and Dialysis, University of Pavia, ICS Maugeri S.P.a., Pavia, Italia.

Maria Gerosa (M)

Division of Clinical Rheumatology, ASST Istituto Gaetano Pini - CTO, Milan, Italy.
Department of Clinical Sciences and Community Health, University of Milan, ASST Istituto Gaetano Pini - CTO, Milan, Italy.

Roberto Caporali (R)

Division of Clinical Rheumatology, ASST Istituto Gaetano Pini - CTO, Milan, Italy.
Department of Clinical Sciences and Community Health, University of Milan, ASST Istituto Gaetano Pini - CTO, Milan, Italy.

Andrea Doria (A)

Division of Rheumatology, Department of Medicine, DIMED, University of Padua, Padua, Italy.

Piergiorgio Messa (P)

Divisione di Nefrologia e Dialisi-Padiglione Croff, Fondazione Ca' Granda IRCCS Ospedale Maggiore Policlinico Milano, Via della Commenda 15, 20122, Milano, Italy.

Marta Mosca (M)

Department of Clinical and Experimental Medicine, Rheumatology Unit, University of Pisa, Pisa, Italy.

Gabriella Moroni (G)

Divisione di Nefrologia e Dialisi-Padiglione Croff, Fondazione Ca' Granda IRCCS Ospedale Maggiore Policlinico Milano, Via della Commenda 15, 20122, Milano, Italy. gabriella.moroni@policlinico.mi.it.

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