Table 1

Baseline characteristics and demographics of infliximab-treated and etanercept-treated patients with SpA and reason for discontinuation

Infliximab n=1319Etanercept n=1015
INF (n=320)CT-P13 (n=999)ETN (n=493)SB4 (n=522)
Age (years)42 (14)42 (13)41 (14)41 (14)
Disease duration (years)13 (12)10 (11)12 (12)11 (12)
Sex, men, n (%)183 (57)576 (58)235 (48)261 (50)
AS, n (%)183 (57)461 (46)204 (41)199 (38)
nraxSpA or uSpA, n (%)137 (43)538 (54)289 (59)323 (62)
Psoriasis (%)*6375
Inflammatory bowel disease (%)*101122
CRP (mg/L)15 (21)13 (22)11 (18)10 (15)
Patient global (mm)59 (24)64 (24)57 (22)59 (23)
Patient pain (mm)62 (23)59 (24)59 (24)59 (22)
ASDAS3.4 (1.0)3.4 (1.0)3.1 (0.9)3.0 (0.9)
BASDAI (mm)6.0 (2.0)5.6 (2.0)5.4 (2.0)5.4 (1.9)
BASFI (mm)4.4 (2.5)4.8 (2.4)4.1 (2.4)4.1 (2.5)
Concomitant csDMARD, n (%)96 (44)238 (31)98 (29)85 (22)
Country
 Iceland, n (%)5 (2)70 (7)8 (2)0 (0)
 Norway, n (%)2 (1)104 (10)7 (1)20 (4)
 Finland, n (%)21 (7)38 (4)94 (19)0 (0)
 Denmark, n (%)19 (6)546 (55)19 (4)79 (15)
 Sweden, n (%)273 (85)241 (24)365 (74)423 (81)
Reason for discontinuation
 Adverse event, n (%)48 (15)131 (13)33 (7)22 (4)
 Death, n (%)1 (0)0 (0)0 (0)1 (0)
 Inefficacy, n (%)61 (19)139 (14)91 (19)45 (9)
 Pregnancy, n (%)3 (1)4 (0)5 (1)0 (0)
 Remission, n (%)1 (0)0 (0)1 (0)0 (0)
 Non-medical switch, n (%)46 (14)23 (2)81 (16)1 (0)
 Other, n (%)51 (16)70 (7)64 (13)22 (4)
  • Numbers are means (SD) unless otherwise stated.

  • *Comorbidities available from Sweden, Denmark and Finland.

  • AS, ankylosing spondylitis; ASDAS, Ankylosing Spondylitis Disease Activity Score; BASDAI, Bath Ankylosing Spondylitis Disease Activity Index;BASFI, Bath Ankylosing Spondylitis Function Index; CRP, C reactive protein; csDMARD, conventional synthetic disease-modifying antirheumatic drug; CT-P13, infliximab biosimilar; ETN, etanercept originator; INF, infliximab originator; nraxSpA, non-radiographical axial spondyloarthritis; SB4, etanercept biosimilar; SpA, spondyloarthritis; uSpA, undifferentiated spondyloarthritis.