Table 1

Baseline demographics and characteristics*

CharacteristicsTNFi-naïve (n=976)TNFi-previous use (n=298)TNFi-recent use (n=407)All patients (n=1681)
Female, % (n)79 (773)84 (250)82 (333)81 (1356)
Age, years54 (12)53 (12)53 (12)54 (12)
Duration of RA, years8.2 (8.2)11.2 (8.6)11.7 (9.6)9.6 (8.8)
DAS285.9 (1.2)6.2 (1.2)6.0 (1.3)6.0 (1.2)
SJC12.1 (8.7)13.9 (9.6)13.4 (9.9)12.8 (9.2)
TJC21.9 (14.4)24.5 (15.8)23.8 (15.6)22.8 (15.0)
PtGA VAS60.7 (21.0)68.0 (21.4)62.9 (20.8)62.5 (21.2)
PhGA VAS57.3 (17.3)62.9 (17.5)59.5 (18.9)58.8 (17.9)
Pain VAS55.3 (22.3)63.1 (23.4)58.7 (22.0)57.5 (22.6)
CRP, mg/dl1.7 (2.5)2.4 (3.1)2.2 (3.1)1.9 (2.8)
ESR, mm/h37.6 (25.5)42.9 (28.9)40.5 (28.1)39.2 (26.8)
HAQ-DI1.4 (0.6)1.7 (0.6)1.6 (0.6)1.5 (0.6)
Previous DMARDs, n0.5 (0.9)2.5 (1.7)2.5 (1.6)1.3 (1.6)
Background DMARDs, % (n)
 07 (66)21 (62)27 (111)14 (239)
 168 (659)71 (211)62 (254)67 (1124)
 222 (211)5 (16)8 (31)15 (258)
 ≥34 (40)3 (9)3 (11)4 (60)
Patients receiving corticosteroids, % (n)47.0 (459)56.4 (168)48.2 (196)49.0 (823)
Mean corticosteroid dose, mg/day6.837.857.577.22
Leflunomide dose, mg/day18.2 (5.1)18.2 (4.5)19.0 (3.0)18.4 (4.6)
Methotrexate dose, mg/week17.4 (5.3)18.3 (12.9)17.0 (5.8)17.5 (7.3)
Sulfasalazine dose, g/day1.9 (0.6)1.7 (0.6)2.0 (0.6)1.9 (0.6)
Geographical distribution, % (n)
 Canada11.2 (109)10.4 (31)5.9 (24)9.8 (164)
 Western Europe61.3 (598)81.5 (243)87.5 (356)71.2 (1197)
 Other27.6 (269)8.1 (24)6.6 (27)19.0 (320)
  • * Data are presented as mean (SD), unless stated otherwise.

  • Dose is expressed in prednisone equivalents for treated patients.

  • Other includes Australia, Czech Republic, Greece, Hungary, India, Poland, Romania, Saudi Arabia and Turkey.

  • CRP, C-reactive protein; DAS28, disease activity score based on 28 joints; DMARD, disease-modifying antirheumatic drug; ESR, erythrocyte sedimentation rate; HAQ-DI, Health Assessment Questionnaire-Disability Index; IR, inadequate response; PtGA, patient global assessment; PhGA, physician global assessment; RA, rheumatoid arthritis; SJC, swollen joint count; TJC, tender joint count; TNFi, tumour necrosis factor inhibitor; TNFi-naive, patients who had never received TNFi therapy; TNFi-previous use, patients who had discontinued TNFi therapy for >2 months before baseline (washout period); TNFi-recent use, patients who had discontinued TNFi therapy for ≤2 months before baseline (no washout period); VAS, visual analogue scale.