Weaning of maintenance immunosuppressive therapy in lupus nephritis (WIN-Lupus): results of a multicentre randomised controlled trial
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Published:2022-06-20
Issue:10
Volume:81
Page:1420-1427
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ISSN:0003-4967
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Container-title:Annals of the Rheumatic Diseases
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language:en
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Short-container-title:Ann Rheum Dis
Author:
Jourde-Chiche NoemieORCID, Costedoat-Chalumeau NathalieORCID, Baumstarck Karine, Loundou Anderson, Bouillet Laurence, Burtey Stéphane, Caudwell Valérie, Chiche Laurent, Couzi Lionel, Daniel Laurent, Deligny Christophe, Dussol Bertrand, Faguer StanislasORCID, Gobert Pierre, Gondran Guillaume, Huart Antoine, Hummel Aurélie, Kalbacher Emilie, Karras Adexandre, Lambert Marc, Le Guern Véronique, Lebourg Ludivine, Loubière Sandrine, Maillard-Lefebvre Hélène, Maurier François, Pha Micheline, Queyrel Viviane, Remy Philippe, Sarrot-Reynauld Françoise, Verhelst David, Hachulla EricORCID, Amoura Zahir, Daugas EricORCID
Abstract
ObjectivesLupus nephritis (LN) is a frequent complication of systemic lupus erythematosus (SLE). Severe (proliferative) forms of LN are treated with induction immunosuppressive therapy (IST), followed by maintenance IST, to target remission and avoid relapses. The optimal duration of maintenance IST is unknown. The WIN-Lupus trial tested whether IST discontinuation after 2‒3 years was non-inferior to IST continuation for two more years in proliferative LN.MethodsWIN-Lupus was an investigator-initiated multicentre randomised controlled trial. Patients receiving maintenance IST with azathioprine or mycophenolate mofetil for 2–3 years, and hydroxychloroquine, were randomised (1:1) into two groups: (1) IST continuation and (2) IST discontinuation. The primary endpoint was the relapse rate of proliferative LN at 24 months. Main secondary endpoints were the rate of severe SLE flares, survival without renal relapse or severe flare, adverse events.ResultsBetween 2011 and 2016, 96 patients (out of 200 planned) were randomised in WIN-Lupus: IST continuation group (n=48), IST discontinuation group (n=48). Relapse of proliferative LN occurred in 5/40 (12.5%) patients with IST continuation and in 12/44 (27.3%) patients with IST discontinuation (difference 14.8% (95% CI −1.9 to 31.5)). Non-inferiority was not demonstrated for relapse rate; time to relapse did not differ between the groups. Severe SLE flares (renal or extrarenal) were less frequent in patients with IST continuation (5/40 vs 14/44 patients; p=0.035). Adverse events did not differ between the groups.ConclusionsNon-inferiority of maintenance IST discontinuation after 2‒3 years was not demonstrated for renal relapse. IST discontinuation was associated with a higher risk of severe SLE flares.Trial registration numberNCT01284725.
Funder
French Ministry of Health
Subject
General Biochemistry, Genetics and Molecular Biology,Immunology,Immunology and Allergy,Rheumatology
Cited by
46 articles.
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