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Table 1 Baseline demographics

From: Alemtuzumab for refractory primary systemic vasculitis—a randomised controlled dose ranging clinical trial of efficacy and safety (ALEVIATE)

 

All subjects (n = 23)

Low dose (n = 13)

High dose (n = 10)

Age in years (median; IQR)

40.5 (28.0–44.0)

35.0 (25.0–46.5)

41.0 (33.0–44.0)

Sex (M to F)

8:15

6:7

2:8

Disease (AAV to BD)

12:11

6:7

6:4

GPA

8

4

4

MPA

1

1

0

EGPA

3

1

2

BD

11

7

4

BVAS/WG score at entry (median; IQR)

4.0 (4.0–5.5)

4.0 (4.0–6.0)

4.5 (4.0–5.0)

Prior disease duration in months (median; IQR)

61.0 (42.0–102.5)

76.0 (52.0–115.0)

51.0 (40.0–68.5)

Number of previous treatments received (median; IQR)

4 (3–5)

5 (3–5)

4(3–4.75)

ANCA specificity (PR3:MPO:Neg)

7:1:15

4:1:8

3:0:7

Prior median cumulative cyclophosphamide dose (AAV only) in grams (n = 12)

9.1 (7–19.4)

6.4 (4.2–25.8)

9.6 (8.7–17.3)

Prior median cumulative rituximab dose (AAV only) in grams (n = 12)

4.5 (3–5.75)

5 (3–6)

4 (3–5)

  1. AAV ANCA-associated vasculitis, BD Behçet’s disease, GPA granulomatosis with polyangiitis, MPA microscopic polyangiitis, eGPA eosinophilic granulomatosis with polyangiitis, IQR interquartile range, BVAS/WG Birmingham Vasculitis Activity Score for Wegener’s granulomatosis, PR3 proteinase 3, MPO myeloperoxidase