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Table 1 Demographic and clinical characteristics of RA patients treated with TCZ or TNFIs

From: Head-to-head comparison of the safety of tocilizumab and tumor necrosis factor inhibitors in rheumatoid arthritis patients (RA) in clinical practice: results from the registry of Japanese RA patients on biologics for long-term safety (REAL) registry

Characteristics

TCZ group (number = 302)

TNFI group (number = 304)

P value

Age, years

59.20 ± 13.04

57.33 ± 15.18

0.275

Female, %

82.5

82.8

0.425

Disease duration, years

10.20 ± 8.64

7.96 ± 8.70

<0.001

Steinbrocker’s stagea

51.0

35.2

<0.001

(III or IV), %

Steinbrocker’s classa

29.1

19.4

0.005

(3 or 4), %

Previous biologic use, %

70.5

10.5

<0.001

Number of previous non-biological DMARDs ≥3, %

47.0

38.5

0.034

DAS28CRP (3)b

4.50 ± 1.23 (n = 233)

4.25 ± 1.24 (n = 279)

0.019

Pulmonary diseasesc, %

20.2

15.5

0.128

Diabetes mellitus, %

10.9

10.5

0.873

Liver diseasesd, %

6.6

4.6

0.281

Kidney diseasese, %

3.6

0.7

0.011

MTX use, %

53.0

85.5

<0.001

MTX dose, mg/week

8.41 ± 2.80

8.54 ± 2.28

0.237

Oral corticosteroids use, %

65.6

51.0

<0.001

PSL-equivalent dosef, mg/day

5.32 ± 3.19

4.99 ± 3.05

0.433

  1. aSteinbrocker’s classification was used to define RA disease stages and classes; bDAS28CRP (3) was calculated based on three variables: swollen and tender 28-joint counts and CRP; cpulmonary diseases included interstitial lung disease, chronic obstructive pulmonary disease, and asthma; dliver diseases included hepatitis B carrier, hepatitis C carrier, fatty liver, hepatitis, primary biliary cirrhosis, positive anti-hepatitis C antibody, cholelithiasis, and abnormal liver function tests; ekidney diseases included nephrotic syndrome, nephritis, renal failure, chronic kidney disease, renal hypertension, hemi-kidney, and elevation of serum creatinine; fthe oral corticosteroids dose was converted to the equivalent prednisolone dosage. CRP; C-reactive protein; DAS28, disease activity score including 28-joint count; DMARDs, disease-modifying antirheumatic drugs; MTX, methotrexate; PSL, prednisolone; RA, rheumatoid arthritis; TCZ, tocilizumab; TNFIs, tumor necrosis factor inhibitors.