Table 1

Baseline characteristics of patients in the study population*

AbataceptTocilizumab
CharacteristicsAll patients (n=150)Patients with baseline DAS28 and ≥1 follow-up (n=104)All patients (n=178)Patients with baseline DAS28 and ≥1 follow-up (n=97)
Male sex (n (%))34 (23)23 (22)42 (24)25 (26)
Age (years)55 (22–85)54 (23–82)56 (20–81)56 (20–81)
Disease duration (years)8.5 (1–45)8 (1–38)9 (1–51)7 (1–45)
Number of previous DMARDs3 (0–8)3 (0–8)3 (0–8)3 (1–8)
Previous DMARDs (%)
 Azathioprine1182016
 Cyclophosphamide1133
 Ciclosporin12131112
 Gold19202414
 Hydroxychloroquine45474854
 Leflunomide27292324
 MTX95979698
 Penicillamine1191414
 Sulfasalazine82837980
Number of previous biological drugs2 (0–6)2 (0–6)2 (0–6)2 (0–6)
Previous biological DMARDs (%)
 Abatacept2126
 Adalimumab65646060
 Anakinra81145
 Certolizumab1000
 Etanercept77826875
 Infliximab63635963
 Rituximab16192015
 Tocilizumab73
≥1 TNFα inhibitor (n (%))142 (95)101 (97)166 (93)95 (98)
≥1 Biological drug of any kind (n (%))145 (97)102 (98)169 (95)95 (98)
DAS285.3 (2.6–7.5)5.3 (2.6–7.5)5.4 (1.6–7.8)5.4 (1.6–7.8)
Concomitant MTX (n (%))79 (53)70 (67)87 (49)65 (67)
MTX dosage (mg/week)20 (10–25)17.5 (10–25)20 (10–25)20 (10–25)
Concomitant prednisolone (n (%))56 (37)47 (45)56 (31)37 (38)
Prednisolone dosage (mg/day)7.5 (5–10)7.5 (5–10)7.5 (5–10)6.25 (5–10)
  • * Except where indicated otherwise, values are the median (range).

  • 7% (n=11) of the patients in the abatacept group had previously been treated with tocilizumab and 21% (n=37) of the patients in the tocilizumab group had previously been treated with abatacept.

  • Median (IQR) among patients receiving the drug.

  • DAS28, Disease Activity Score in 28 joints; DMARDs, disease-modifying antirheumatic drugs; MTX, methotrexate; TNFα, tumour necrosis factor α.