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. 2020 Sep 3;11:2053. doi: 10.3389/fimmu.2020.02053

Table 4.

Kaplan-Meier estimates for relapse following a rise in PR3-ANCA*.

ALBIA
Median months to relapse Cumulative Relapse, % (95% C.I.)
N* 6-months 12 months 18 months
Overall
Any relapse 72 15.4 26 (15, 35) 42 (29, 52) 52 (38, 62)
Severe relapse 80 22.1 22 (12, 30) 35 (23, 45) 42 (30, 52)
Baseline capillaritis
Any relapse 58 22.1 23 (11, 33) 36 (22, 48) 44 (29, 56)
Severe relapse 66 24.2 19 (8, 28) 32 (19, 42) 37 (24, 48)
Baseline renal
Any relapse 44 26 (11, 38) 31 (15, 44) 39 (22, 53)
Severe relapse 51 37.0 20 (8, 31) 29 (15, 41) 36 (20, 52)
Baseline DAH
Any relapse 20 10.2 43 (15, 61) 54 (24, 72) 67 (35, 83)
Severe relapse 22 14.3 34 (10, 51) 49 (22, 67) 60 (31, 77)
Rituximab group
Any relapse 37 14.6 22 (7, 35) 42 (24, 57) 55 (34, 69)
Severe relapse 44 21.7 21 (8, 32) 35 (19, 48) 45 (28, 59)
Cyclophosphamide
Any relapse 35 18.2 29 (12, 42) 41 (22, 56) 48 (28, 63)
Severe relapse 36 24.2 22 (7, 35) 34 (16, 48) 38 (19, 52)
*

Analyses include individuals who experienced a rise in PR3-ANCA during follow-up while at risk for the given relapse endpoint. Individuals who experienced an ANCA increase concurrent with the given relapse event are not included. Time zero corresponds to the date of the ANCA increase.