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Sökning: id:"swepub:oai:DiVA.org:liu-141703" > Randomised controll...

Randomised controlled trial of prolonged treatment in the remission phase of ANCA-associated vasculitis

Karras, Alexandre (författare)
Hop Europeen Georges Pompidou, France; University of Paris 05, France
Pagnoux, Christian (författare)
Mt Sinai Hospital, Canada
Haubitz, Marion (författare)
Klinikum Fulda, Germany; Klinikum Fulda, Germany
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de Groot, Kirsten (författare)
Klinikum Offenbach, Germany
Puechal, Xavier (författare)
Hop Cochin, France
Cohen Tervaert, Jan Willem (författare)
Maastricht University, Netherlands
Segelmark, Mårten (författare)
Linköpings universitet,Avdelningen för läkemedelsforskning,Medicinska fakulteten,Region Östergötland, Njurmedicinska kliniken US
Guillevin, Loic (författare)
University of Paris 05, France; Hop Cochin, France
Jayne, David (författare)
University of Cambridge, England
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 (creator_code:org_t)
2017-05-25
2017
Engelska.
Ingår i: Annals of the Rheumatic Diseases. - : BMJ PUBLISHING GROUP. - 0003-4967 .- 1468-2060. ; 76:10, s. 1662-1668
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Objectives A prospective randomised trial to compare two different durations of maintenance immunosuppressive therapy for the prevention of relapse in anti-neutrophil cytoplasmic antibodies (ANCA)associated vasculitis (AAV). Methods Patients with AAV were recruited 18-24 months after diagnosis if they were in stable remission after cyclophosphamide/prednisolone-based induction followed by azathioprine/prednisolone maintenance therapy. They were randomised (1: 1) to receive continued azathioprine/prednisolone to 48 months from diagnosis (continuation group) or to withdraw azathioprine/prednisolone by 24 months (withdrawal group). The primary endpoint was the relapse risk, from randomisation to 48 months from diagnosis. Results One hundred and seventeen patients were randomised and 110 remained to the trial end. At entry, median serum creatinine was 116 mu mol/L (range 58-372), 53% were ANCA positive. The percentage of patients presenting with relapse was higher in the withdrawal than in the continuation treatment group (63% vs 22%, pamp;lt;0.0001, OR 5.96, 95% CI 2.58 to 13.77). ANCA positivity at randomisation was associated with relapse risk (51% vs 29%, p=0.017, OR 2.57, 95% CI 1.16 to 5.68). Renal function, ANCA specificity, vasculitis type and age were not predictive of relapse. Severe adverse events were more frequent in the continuation than withdrawal groups (nine vs three events), but the continuation group had better renal outcome (0 vs 4 cases of end-stage renal disease), with no difference in patient survival. Conclusions Prolonged remission maintenance therapy with azathioprine/prednisolone, beyond 24 months after diagnosis reduces relapse risk out to 48 months and improves renal survival in AAV.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Reumatologi och inflammation (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Rheumatology and Autoimmunity (hsv//eng)

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