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Table 2 Patients’ characteristics by rituximab indication

From: Real-life drug retention rate and safety of rituximab when treating rheumatic diseases: a single-centre Swiss retrospective cohort study

 

RA n = 105

CTD n = 60

Vasculitis n = 20

Other n = 18

Comparison between groups

Age at time of first RTX, years, mean (SD)

57.8 (13.9)

48.0 (14.3)

57.4 (14.1)

56.2 (13.7)

p = 0.0003

Female, n (%)

82 (78.1)

55 (91.7)

10 (50.0)

11 (61.1)

p < 0.0001

Time between diagnosis and first RTX, years, median [range]

7.3 [0.3, 46.5]

5.0 [0.1, 38.7]

0.4 [0.02, 10.8]

2.4 [0.4, 31.1]

p = 0.0001

Previous treatments, n (%)

 Glucocorticoids

87/91 (95.6)

51/59 (86.4)

19 (95.0)

14 (77.8)

p = 0.045

 csDMARD (any)

103 (98.1)

55 (91.7)

6 (30.0)

14 (77.8)

p < 0.0001

 Cyclophosphamide

0

4 (6.7)

11 (55.0)

2 (11.1)

p < 0.0001

 Anti-TNF agent

88/103 (85.4)

18 (30.0)

0

6 (33.3)

p < 0.0001

 Other biological agents

30 (28.6)

6 (10.0)

0

5 (27.8)

p = 0.003

Initial RTX regimen

    

p < 0.0001

 1000 mg/15 days (× 2)

102 (97.1)

50 (83.3)

8 (40.0)

14 (77.8)

 

 375 mg/m2/week (× 4)

0

5 (8.3)

11 (55.0)

4 (22.2)

 

 other

3 (2.9)

5 (8.3)

1 (5.0)

0

 

Concomitant treatments, n (%)

 Glucocorticoids

56/94 (59.6)

41/55 (74.6)

19 (95.0)

7/16 (43.8)

p = 0.002

 csDMARD (any)

71 (67.6)

39 (65.0)

3 (15.0)

6 (33.3)

p < 0.0001

 Methotrexate

46/98 (46.9)

14/59 (23.7)

1 (5.0)

2/16 (12.5)

p < 0.0001

 None

12 (11.4)

5 (8.3)

1 (5.0)

6 (33.3)

p = 0.02

IgG levels before RTX initiation, g/l, mean (SD)

11.3 (3.9) n = 94

13.7 (7.8) n = 52

9.6 (4.4) n = 17

9.6 (2.7) n = 14

p = 0.05

Hypogammaglobulinaemia before RTX initiation, n (%)

    

p = 0.002

 None

84/94 (89.4)

44/52 (84.6)

12/17 (70.6)

12/14 (85.7)

 

 Mild (5–6.9 g/l)

10/94 (10.6)

7/52 (13.5)

2/17 (11.8)

2/14 (14.3)

 

 Moderate to severe (< 5 g/l)

0

1/52 (1.9)

3/17 (17.7)

0

 
  1. RA Rheumatoid arthritis, CTD Connective tissue disease, RTX Rituximab