Table 2.

Patient characteristics and medication use of patients starting biologic treatment in the years 2015 and 2017.

Before Introduction of Biosimilar, n = 59After Introduction of Biosimilar, n = 67
NN
Baseline characteristics
      Mean (SD) age at biologic initiation, yrs52 (14)5958 (14)67
      Mean (SD) disease duration at biologic initiation, yrs4 (6)594 (6)67
      Female sex, %74.64470.147
      RF positive, %42.322/5256.422/39
      Anti-CCP positive, %51.927/5255.625/45
      BMI, mean (SD)27.0 (7)4027.8 (7)35
      DAS28 at biologic initiation, mean (SD)4.7 (1.3)384.5 (1.2)42
Medication use prior to initiation of first bDMARD
      No. csDMARDs used, mean (SD)2.1 (0.7)572.1 (0.7)60
      Patients with GC treatment in last year, %73437349
      No. prednisone prescriptions in last year, mean (SD)2.7 (2.5)592.6 (2.6)67
Medication use during initiation of first bDMARD
Distribution of bDMARD utilization at initiation of first bDMARD
      Abatacept––21
      Adalimumab53314228
      Etanercept36214631
      Certolizumab––32
      Golimumab3221
      Infliximab21––
      Rituximab5332
      Tocilizumab2132
No. csDMARD at biologic initiation (co-medication)
      01482718
      144263725
      242253524
Patients using MTX at biologic initiation, %68405436
  • Anti-CCP: anticyclic citrullinated peptide antibody; bDMARD: biologic disease-modifying antirheumatic drug; csDMARD: conventional synthetic disease-modifying antirheumatic drug; DAS28: Disease Activity Score in 28 joints; GC: glucocorticoid; MTX: methotrexate; RF: rheumatoid factor.