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Table 4 Switching between TNF and non-TNF biologic DMARDs

From: Factors associated with initial or subsequent choice of biologic disease-modifying antirheumatic drugs for treatment of rheumatoid arthritis

Prior biologic

Number (% of all prior biologic DMARDs)

Number of switches (% of each prior biologic DMARD)

Adjusteda OR of any switch (95% CI)

Switch to TNF or to non-TNF inhibitorsb

Number of switches to TNF inhibitors (%)

Number of switches to non-TNF inhibitors (%)

TNF inhibitors

 Etanercept

11,753 (50.6)

1223 (10.4)

Reference

989 (80.9)

234 (19.1)

 Adalimumab

5119 (22.0)

732 (14.3)

1.22 (1.10, 1.35)

573 (78.3)

159 (21.7)

 Certolizumab

104 (0.4)

20 (19.2)

1.44 (0.86, 2.39)

8 (40.0)

12 (60.0)

 Golimumab

130 (0.6)

35 (26.9)

2.24 (1.48, 3.37)

22 (62.9)

13 (37.1)

 Infliximab

5102 (22.0)

567 (11.1)

1.06 (0.95, 1.19)

377 (66.5)

190 (33.5)

Non-TNF inhibitor biologic agents

 Abatacept

407 (1.8)

70 (17.2)

1.31 (0.99, 1.72)

40 (57.1)

30 (42.9)

 Anakinra

260 (1.1)

85 (32.7)

3.20 (2.41, 4.25)

79 (92.9)

6 (7.1)

 Rituximab

334 (1.4)

27 (8.1)

0.57 (0.38, 0.85)

16 (59.3)

11 (40.7)

 Tocilizumab

22 (0.1)

2 (9.1)

0.59 (0.14, 2.60)

0 (0.0)

2 (100)

Total

23231 (100)

2761 (11.9)

743 (76.2)

657 (23.8)

  1. DMARD disease-modifying antirheumatic drug. aAdjusted for demographics, data source, calendar year, comorbidities, history of medication use, and healthcare utilization in the baseline period. bTNF inhibitors include adalimumab, certolizumab, etanercept, golimumab, and infliximab; non-TNF inhibitors include abatacept, anakinra, rituximab, and tocilizumab