Table II.
All patients | Type of vasculitis |
||||||
---|---|---|---|---|---|---|---|
GPA | MPA | EGPA | GCA | TAK | PAN | ||
| |||||||
Number of patients (%) | 93 | 45 | 8 | 12 | 14 | 9 | 5 |
Efficacy at 6 months | 62 (67%) | 31 (69%) | 6 (75%) | 4 (33%) | 9 (64%) | 8 (89%) | 4 (80%) |
Reason for treatment inefficacy | |||||||
Active disease | 19 (20%) | 7 (16%) | - | 6 (50%) | 4 (29%) | 1 (1%) | 1 (20%) |
Adverse events | 12 (13%) | 7 (16%) | 2 (25%) | 2 (17%) | 1 (7%) | 0 | 0 |
Sustained remission at 12 months | 54 (58%) | 27 (63%) | 6 (75%) | 4 (33%) | 7 (54%) | 8 (89%) | 3 (60%) |
Sustained remission at 24 months | 46 (50%) | 23 (58%) | 5 (71%) | 4 (33%) | 7 (54%) | 7 (88%) | 2 (40%) |
Given percentages are for the proportion of patients in each type of vasculitis with available data, which was incomplete at 12 and/or 24 months for 7 individuals (2 lost to follow-up after 12 months [MPA and TAK]; 4 had not yet reached 12 and/or 24 months with LEF [3 GPA and 1 GCA]; one with GPA died of natural causes before 24 months of LEF).
EGPA: eosinophilic granulomatosis with polyangiitis; GCA: giant cell arteritis; GPA: granulomatosis with polyangiitis; MPA: microscopic polyangiitis; PAN: polyarteritis nodosa; TAK: Takayasu’s arteritis.