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Arthritis Rheumatol. 2019 Jan 22. doi: 10.1002/art.40802. [Epub ahead of print]

Efficacy and Safety of Belimumab and Azathioprine for Maintenance of Remission in ANCA-Associated Vasculitis: A Randomized Controlled Study.

Author information

1
Department of Medicine, University of Cambridge, Cambridge, UK.
2
University Hospital Gasthuisberg, Leuven, Belgium.
3
Botnar Research Centre, University of Oxford, Oxford, UK.
4
Clinic of Nephrology, Internal and Occupational Diseases, Sechenov First Moscow State Medical University, Moscow, Russian Federation.
5
GSK, Stockley Park, UK.
6
GSK, Stevenage, UK.
7
GSK, Collegeville, PA, USA.
8
Division of Rheumatology, and the Department of Biostatistics, Epidemiology, and Informatics, University of Pennsylvania, Philadelphia, PA, USA.

Abstract

OBJECTIVE:

To evaluate safety and efficacy of belimumab as adjunctive therapy to maintain remission in antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV).

METHODS:

This double-blind, placebo-controlled, multicenter study (BEL115466/NCT01663623) randomized (1:1) patients (≥18 years) with AAV following remission induction with rituximab/cyclophosphamide and glucocorticoids. Patients received azathioprine 2 mg/kg/day, oral glucocorticoids, and placebo/intravenous belimumab 10 mg/kg. Primary endpoint was time to first protocol-specified event (PSE), defined as Birmingham Vasculitis Activity Score (BVAS) ≥6, ≥1 major BVAS item, or receipt of prohibited medication (adjusted for ANCA type [proteinase 3 (PR3)/myeloperoxidase (MPO)], disease stage at induction, and induction regimen). Vasculitis relapse was defined as PSE BVAS activity, or receipt of prohibited medications for vasculitis. Changes in treatment practice led to study truncation from 300 to ~100 patients.

RESULTS:

The intention-to-treat population totaled 105 patients (placebo, 52 [40 PR3-ANCA; 12 MPO-ANCA]; belimumab, 53 [41 PR3-ANCA; 12 MPO-ANCA]: induced by rituximab, 27; cyclophosphamide, 78. Compared with placebo, belimumab did not reduce PSE risk (adjusted HR=1.07; 95% CI: 0.44, 2.59; p=0.884) or vasculitis relapse (adjusted HR=0.88; 95% CI: 0.29, 2.65; p=0.821); overall PSE rate was low (placebo, 11/52 [21.2%]; belimumab 10/53 [18.9%]). Vasculitis relapse in the placebo group (n=8) occurred independently of induction regimen/disease stage, or ANCA type. All vasculitis relapses in the belimumab group (n=6) were in cyclophosphamide-induced, anti-PR3-ANCA-associated patients. Adverse events occurred in 49/53 belimumab (92.5%) and 43/52 placebo (82.7%) recipients, with no new safety concerns.

CONCLUSION:

Belimumab plus azathioprine and glucocorticoids for the maintenance of remission in AAV did not reduce risk of relapse. This article is protected by copyright. All rights reserved.

KEYWORDS:

ANCA-Associated Vasculitis; B-Lymphocyte; Randomized Trial; Vasculitis

PMID:
30666823
DOI:
10.1002/art.40802

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