Table 1

Baseline characteristics

Add-on (N=277)Switch (N=276)
Women, n (%)227 (81.9)217 (78.6)
Age (years), mean (SD)53.0 (13.4)53.6 (11.9)
Patients aged ≥65 years, n (%)53 (19.1)52 (18.8)
BMI, kg/m², mean (SD)26.3 (5.20)26.5 (5.14)
Duration of RA (years), mean (SD)8.2 (8.0)8.3 (8.4)
Categorical duration of RA (years), n (%):
 <251 (18.4)66 (23.9)
 ≥2 to <576 (27.4)68 (24.6)
 ≥5 to <1066 (23.8)63 (22.8)
 ≥1084 (30.3)79 (28.6)
Swollen joint count, mean (SD)14.4 (8.9)15.3 (10.2)
Tender joint count, mean (SD)25.8 (13.9)26.6 (15.2)
DAS28-ESR, mean (SD)6.33 (0.98)6.36 (1.00)
HAQ-DI, mean (SD)1.46 (0.65)1.48 (0.60)
Fatigue,* n (%)117 (75.0)110 (73.3)
Genant-modified Sharp score, mean (SD)30.8 (32.2)37.2 (40.6)
MTX dose, mg/week, mean (SD)16.1 (4.4)16.3 (4.2)
MTX dose, mg/week, median15.015.0
Number of previous DMARDs (including MTX prior to study entry), mean (SD)1.9 (1.1)1.9 (1.0)
Oral steroid use, n (%)140 (50.5)140 (50.7)
Rheumatoid factor positive,† n (%)55 (66.3)41 (64.1)
Anti-CCP positive,† n (%)68 (81.9)49 (76.6)
  • *Assessed by the proportion of patients answering ‘yes’ to question 21 of the Rheumatoid Arthritis Quality of Life questionnaire (‘I feel tired whatever I do’).

  • †Of 147 patients (27%) with available retrospective data.

  • BMI, body mass index; CCP, anticyclic citrullinated peptide; DAS28-ESR, Disease Activity Score based on 28 joints-erythrocyte sedimentation rate; DMARD, disease-modifying antirheumatic drug; HAQ-DI, Health Assessment Questionnaire-disability index; MTX, methotrexate; PBO, placebo; RA, rheumatoid arthritis.