Skip to main content
. 2020 May 6;6(1):e001136. doi: 10.1136/rmdopen-2019-001136

Table 2.

Comparing study features of anti-TNF trials in pSpA

CRESPA trial13 55 ABILITY-2 trial33 Paramarta et al35 54
Inclusion criteria ASAS classification criteria + rheumatologist diagnosis ASAS classification criteria + no prior psoriasis, PsA or AS ESSG or Amor criteria + no AS or PsA
Multicenter study No Yes No
Anti-TNF-blocking agent Golimumab Adalimumab Adalimumab
Number of included patients 60 165 40
Symptom duration (mean ± SD years) 5.2 weeks ±2.8 vs 4.4 weeks ±2.0 6.6 years ±6.3 vs 7.7 years ±7.9 7.9 years ±9.3 vs 6.7 years ±6.2
Primary end point
% patients in clinical remission at w24
% patient PSpARC40 response at w12
PGA of disease activity
Absence of arthritis, dactylitis and enthesitis at w24
75% vs 20% (p<0.001)
57.5% vs 20% (p=0.0069)
−50.0 vs −20.0 (p=0.0015)
PSpARC40 response criteria at w12
ND
39% vs 20% (p=0.006)
−27.5 vs −16.4 (p=0.003)
PGA of disease activity
ND
ND
−31.0 vs −5.9 (p=0.001)
Withdrawal strategy
Relapse rate after discontinuation
Yes
47%
No Yes
73%

AS, ankylosing spondylitis; ASAS, Assessment of Spondyloarthritis International Society; ESSG criteria, European Spondylitis Study Group criteria; PSpARC40 response criteria, peripheral spondyloarthritis 40% response criteria.