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Table 2 Characteristics of first prescribed bDMARD, comparing etanercept and other TNFis

From: Biologic switching patterns among children with non-systemic juvenile idiopathic arthritis

Biologic

Etanercept

Other TNFi

P-value*

N

99

101

 

Age at diagnosis, median years (IQR)

5.0 (2.3–9.9)

9.7 (3.4–13.7)

< 0.001

Disease duration, median years (IQR)

7.3 (4.7–10.1)

4.9 (3.3–8.7)

0.001

Active joints at start of 1st bDMARD, median (IQR)

2 (1–4)

2 (1–3)

0.592

Cumulative active joints, median (IQR)

6 (3–11)

5 (2–7)

0.093

Switchers, n (%)

49 (49)

25 (25)

< 0.001

0 switch

50 (51)

76 (75)

0.014

1 switch

27 (27)

12 (12)

 

2 switches

14 (14)

9 (9)

 

3 switches

8 (8)

4 (4)

 

Reasons for 1st switch, n (%)

Inefficacy

25 (51)

17 (68)

0.164

Other reasons than inefficacya

24 (49)

8 (32)

 

Disease duration before 1st bDMARD, median months (IQR)

27.5 (5.6–71.3)

21.5 (5.1–51.9)

0.484

Treatment duration of 1st bDMARD, median months (IQR)

24.8 (7.6–44.7)

22.7 (11.7–31.8)

0.540

- Switchers

10.2 (5.8–31.7)

16.2 (8.4–33.7)

0.275

- Non-switchers

35.1 (21.6–51.9)

24.1 (14.0–30.9)

0.002

csDMARD before 1st bDMARD, n (%)

92 (93)

81 (80)

0.003

csDMARD + 1st bDMARD, n (%)

79 (80)

79 (78)

0.559

  1. bDMARD Biological disease-modifying antirheumatic drugs, TNFi Tumor necrosis factor inhibitor, IQR 1st-3rd interquartile range, csDMARD Conventional synthetic disease-modifying anti-rheumatic drugs
  2. *P-value for comparison of switchers to non-switchers, by Pearson’s Chi2 for categorical variables and Mann-Whitney U-test for continuous variables
  3. aOther reasons for switching than inefficacy included injection/infusion reactions, severe adverse events, psychological factors, non-compliance, uveitis, IBD