Table 2

Effect of TNFi on ASAS20, ASAS40 and BASFI in patients with nr-axSpA (ASAS criteria) (RCTs)

Outcome
Drug
N patients (Study)Time point (weeks)Response treatment (%)Response placebo (%)RR (95% CI)NNT
ASAS20
 Etanercept215 (EMBARK25)1252.436.11.45 (1.06 to 1.90)6.1
 Infliximab*
 Adalimumab185 (ABILITY-127)1251.630.91.67 (1.17 to 2.40)4.8
 Golimumab198 (GO-AHEAD28)1671.140.01.78 (1.43 to 2.43)3.2
 Certolizumab96† (RAPID-axSpA22)2465.224.02.72 (1.59 to 4.65)2.4
ASAS40
 Etanercept215 (EMBARK25)1233.314.82.25 (1.33 to 3.81)5.4
 Infliximab*40 (Barkham 200926)1661.117.63.47 (1.16 to 10.31)2.3
 Adalimumab185 (ABILITY-127)1236.314.92.44 (1.40 to 4.25)4.7
 Golimumab198 (GO-AHEAD28)1656.723.02.47 (1.67 to 3.70)3.0
 Certolizumab96† (RAPID-axSpA22)2456.514.04.04 (1.94 to 8.40)2.7
Impr. mean (SD)Impr. mean (SD)SMD (95% CI)
BASFI (Δ‡)
 Etanercept215 (EMBARK25)121.40 (0.2)0.80 (0.2)3.00 (2.61 to 3.39)
 Infliximab*40 (Barkham 200926)162.70 (2.36)0.47 (2.25)0.97 (0.31 to 1.62)
 Adalimumab185 (ABILITY-127)121.10 (−)0.60 (−)n/e
 Golimumab
 Certolizumab96† (RAPID-axSpA22)242.50 (2.4)0.10 (2.3)1.02 (0.59 to 1.44)
  • *nr-axSpA defined by: inflammatory back pain (Calin definition) within 3 months to 3 years AND sacroiliitis on MRI AND HLA-B27 positivity.

  • †Certolizumab pegol 200 mg versus placebo.

  • ‡Mean improvement compared to baseline value (range: 0–10).

  • ASAS, Assessment in SpondyloArthritis international Society; BASFI, Bath Ankylosing Spondylitis Functional Index; HLA, human leucocyte antigen; Impr, improvement; NA, not applicable; n/e, not possible to estimate; nr-axSpA, non-radiographic axial spondyloarthritis; NNT, number needed to treat; RR, risk ratio; SMD, standardised mean difference.