Table I.
Characteristics | Values |
---|---|
| |
Demographic features | |
Age at diagnosis, 4 mean ± SD [range], years | 48 ± 19.3 [4–80] |
Number of females | 66 (71%) |
Race | |
Caucasian | 73 (79%) |
Asian | 6 (7%) |
Black or African American | 4 (4%) |
Vasculitis diagnosis | |
Granulomatosis with polyangiitis | 45 (48%) |
ANCA-positive | 31 (33%) |
Microscopic polyangiitis | 8 (9%) |
ANCA-positive | 8 (9%) |
Eosinophilic granulomatosis with polyangiitis | 12 (13%) |
Takayasu’s arteritis | 9 (10%) |
Giant cell arteritis | 14 (15%) |
Polyarteritis nodosa | 5 (5%) |
Previous treatments | |
Glucocorticoids | 87 (94%) |
Oral or intravenous cyclophosphamide | 65 (70%) |
Methotrexate | 64 (69%) |
Azathioprine | 51 (55%) |
Rituximab | 15 (16%) |
Mycophenolate mofetil | 12 (13%) |
Infliximab | 6 (7%) |
Others* | 21 (23%) |
Data are n (%) of patients, unless otherwise indicated.
n=4: hydroxychloroquine; n=4: intravenous immunoglobulin; n=3: plasma exchange; n=3: etanercept; n=2: tocilizumab; n=3: sulfasalazine; n=1: cyclosporine; and n=1: eculizumab (in a paediatric patient with severe refractory GPA).