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Table 1 Baseline demographics and disease characteristics for the treatment groups assessed (all patients)

From: Health-related quality of life in patients with giant cell arteritis treated with tocilizumab in a phase 3 randomised controlled trial

 

TCZ-QW + Pred-26

N = 100

PBO + Pred-26

N = 50

PBO + Pred-52

N = 51

Age, years

69.5 (8.5)

69.3 (8.1)

67.8 (7.7)

Female, n (%)

78 (78.0)

38 (76.0)

37 (72.5)

Race, n (%)

 White

97 (97.0)

50 (100.0)

49 (96.1)

 Black or African American

1 (1.0)

0

2 (3.9)

 Asian

0

0

0

 Other

1 (1.0)

0

0

 Unknown

1 (1.0)

0

0

Weight, kg

69.8 (13.8)

70.1 (15.8)

73.1 (15.3)

Disease duration, days

306.8 (563.5)

364.7 (569.9)

255.2 (435.5)

Disease onset, n (%)

 Newly diagnosed

47 (47.0)

23 (46.0)

23 (45.1)

 Relapsing

53 (53.0)

27 (54.0)

28 (54.9)

Prednisone dose, mg/day

34.6 (13.4)

34.6 (13.0)

34.5 (14.2)

Cranial signs or symptoms, n (%)

41 (41.0)

20 (40.0)

16 (31.4)

PMR symptoms

59 (59.0)

30 (60.0)

35 (68.6)

ESR, mm/h

24.6 (18.7)

28.8 (25.4)

24.2 (18.2)

SF-36 PCS

43.1 (9.4)

42.6 (10.9)

41.1 (10.0)

SF-36 MCS

42.8 (12.4)

42.7 (12.1)

40.5 (13.7)

FACIT-Fatigue

36.1 (11.1)

35.0 (12.8)

31.4 (13.6)

PtGA, 100 mm VAS

43.6 (25.7)

35.7 (28.2)

47.8 (27.8)

  1. Data are mean (SD) unless stated otherwise
  2. ESR erythrocyte sedimentation rate, FACIT Functional Assessment of Chronic Illness Therapy, MCS Mental Component Summary, PBO placebo, PCS Physical Component Summary, PMR polymyalgia rheumatica, Pred-26 26-week prednisone taper, Pred-52 52-week prednisone taper, PtGA Patient Global Assessment of Disease Activity, QW every week, SD standard deviation, SF-36 36-Item Short-Form Health Survey, TCZ tocilizumab, VAS visual analogue scale