Table 1

Characteristics of the study population

Patients with a follow up of at least 6 months (n=773)Patients with available data to evaluate a EULAR response (n=558)Patients without available data to evaluate EULAR response (n=215)p Value
Age (years), median (IQR)58.0 (49.0–68.0) (0.4%)58.0 (49.0–67.0) (0.4%)58.0 (49.0–70.0) (0.5%)0.4
Female (%)78.7 (0.3%)79.7 (0.4%)76.3 (0.0%)0.3
Disease duration (years), median (IQR)14.0 (8.0–21.0) (1.7%)14.0 (9.0–20.0) (1.3%)14.0 (7.0–22.0) (2.8%)0.9
RF-positivity (%)72.5 (11.6%)72.0 (8.6%)74.0 (19.5%)0.6
Anti-CCP positivity (%)70.2 (20.1%)70.2 (16.3%)70.2 (29.8%)0.9
Number of previous synthetic DMARDs, median (IQR)3.0 (2.0–4.0) (7.2%)3.0 (2.0–4.0) (5.5%)2.5 (1.0–4.0) (11.6%)0.0006
% of 0/1/2/3 previous anti-TNF
None11.411.112.20.6
121.621.721.5
237.737.338.3
329.3 (0.1%)29.9 (0.0%)28.0 (0.5%)
% of patients previously treated with RTX30.1 (0.1%)30.6 (0.0%)28.5 (0.5%)0.6
Concomitant treatment with corticosteroids* (%)75.8 (1.8%)75.5 (1.1%)76.3 (3.7%)0.8
Median dosage (mg/d)8.0 (2.0–10.0) (3.5%)8.0 (2.0–10.0) (2.1%)8.0 (2.3–10.0) (7.0%)0.8
Concomitant treatment with a synthetic DMARD* (%)64.8 (1.4%)65.9 (1.1%)61.9 (2.3%)0.7
Methotrexate**76.376.675.4
Leflunomide**14.614.016.2
Combination/others**9.19.48.4
DAS28 vs ESR at initiation of ABA, median (IQR)5.4 (4.5–6.3) (15.9%)5.4 (4.4–6.3) (0%)5.4 (4.7–6.0) (57.2%)0.9
  • Results are median (IQR) or %. Proportions of missing values are in brackets ().

  • ** Proportion of treated patients among those treated with a synthetic DMARD

  • * Defined as the day of ABA first infusion.

  • ABA, abatacept; anti-CCP, anti-cyclic citrullinated peptide; DAS28, 28-joint disease activity score; DMARD, disease modifying anti-rheumatic drugs; ESR, erythrocyte sedimentation rate; EULAR, European League Against Rheumatism; RF, rheumatoid factor; RTX, rituximab; TNF, tumour necrosis factor.