Table 1

Baseline characteristics of tofacitinib-treated and tocilizumab-treated patients with RA, grouped by the status of previous bDMARD use, before propensity score matching

bDMARD-naïve patients (n=215)Previous bDMARD-failure patients (n=249)
Tofacitinib
(n=93)
Tocilizumab
(n=122)
P value*ASDTofacitinib
(n=154)
Tocilizumab
(n=95)
P value*ASD
Baseline characteristics
 Age, years, mean (SD)63.6 (13.7)64.8 (13.6)0.520.08866.7 (11.5)61.6 (12.5)0.0010.43
 Male sex, number (%)20 (21.5)39 (32.0)0.0930.2033 (21.4)18 (18.9)0.750.051
 RA duration, years, mean (SD)8.8 (10.4)7.8 (8.9)0.470.1013.9 (9.7)11.2 (8.8)0.0300.29
 Advanced stage, number (%)31 (33.3)33 (27.0)0.370.1197 (63.0)50 (52.6)0.110.17
 Anti-CCP-positive, number (%)78 (83.9)97 (79.5)0.480.095135 (87.7)83 (87.4)1.000.007
 RF-positive, number (%)81 (87.1)99 (81.1)0.270.15128 (83.1)81 (85.3)0.720.049
 CDAI, mean (SD)22.7 (9.6)23.0 (10.4)0.820.03023.1 (10.2)22.6 (9.9)0.730.050
 High CDAI (>22), number (%)38 (40.9)55 (45.1)0.580.07076 (49.4)39 (41.1)0.240.14
Concurrent MTX use, number (%)63 (67.7)75 (61.5)0.390.1184 (54.5)66 (69.5)0.0230.25
Concurrent PSL use, number (%)27 (29.0)64 (52.5)0.0010.4142 (27.3)44 (46.3)0.0030.33
  • *Comparisons of each of the baseline characteristics between the tofacitinib and tocilizumab groups, separately in bDMARD-naïve patients and bDMARD-failure patients, using the independent-measures t-test for continuous variables and the χ2 test for categorical variables.

  • †ASD of <0.1 indicates that the baseline characteristic was well balanced between the two treatment groups (tofacitinib vs tocilizumab).

  • ‡Advanced stage was defined as Steinbrocker radiological stages III and IV.

  • anti-CCP, anti-cyclic citrullinated peptide antibodies; ASD, absolute standardised difference; bDMARD, biological disease-modifying antirheumatic drug; CDAI, clinical disease activity index; MTX, methotrexate; PSL, prednisolone; RA, rheumatoid arthritis; RF, rheumatoid factor.