Table 3

Summary of efficacy at week 24 and week 52 among randomised patients by number of prior biological anti-TNF exposure (1 vs >1)

Placebo→UST 45 mgUST 45 mgUST 90 mgCombined UST
Week 24 (N)626058118
ACR20 response by number of prior biological anti-TNF agents
 1 prior agent3/30 (10.0)8/23 (34.8)10/28 (35.7)18/51 (35.3)
 >1 prior agent6/32 (18.8)14/37 (37.8)10/30 (33.3)24/67 (35.8)
PASI75 response by number of prior biological anti-TNF agents*
 1 prior agent0/27 (0.0)7/15 (46.7)12/21 (57.1)19/36 (52.8)
 >1 prior agent1/23 (4.3)13/29 (44.8)8/20 (40.0)21/49 (42.9)
HAQ-DI change from baseline by number of prior biological anti-TNF agents
 1 prior agent (n)30
0.00 (0.00 to 0.25)
23
−0.13 (−0.38 to 0.00)
28 −0.25 (−0.50 to 0.00)51
−0.25 (−0.50 to 0.00)
 >1 prior agent (n)32
0.00 (−0.13 to 0.00)
37
−0.13 (−0.38 to 0.00)
30
0.00 (−0.38 to 0.00)
67
−0.13 (−0.38 to 0.00)
Week 52 (N) 43†6058118
ACR20 response by number of prior biological anti-TNF agents
 1 prior agent12/22 (54.5)11/21 (52.4)14/28 (50.0)25/49 (51.0)
 >1 prior agent4/18 (22.2)9/33 (27.3)8/26 (30.8)17/59 (28.8)
PASI75 response by number of prior biological anti-TNF agents*
 1 prior agent8/20 (40.0)5/13 (38.5)12/21 (57.1)17/34 (50.0)
 >1 prior agent5/10 (50.0)8/23 (34.8)8/19 (42.1)16/42 (38.1)
HAQ-DI change from baseline by number of prior biological anti-TNF agents
 1 prior agent (n)22
0.00 (−0.13 to 0.13)
21
−0.25 (−0.50 to 0.00)
28
−0.19 (−0.50 to 0.00)
49
−0.25 (−0.50 to 0.00)
 >1 prior agent (n)18
0.00 (−0.13 to 0.13)
33
−0.13 (−0.38 to 0.00)
26
0.00 (−0.50 to 0.00)
59
0.00 (−0.50 to 0.00)
  • Data are reported as n (%), n/N (%) or median (IQR).

  • *Among patient with ≥3% BSA psoriasis skin involvement at baseline.

  • †Excludes patients who did not receive ustekinumab.

  • ACR, American College of Rheumatology; BSA, body surface area; HAQ-DI, Health Assessment Questionnaire-Disability Index; PASI, Psoriasis Area and Severity Index; TNF, tumour necrosis factor-α; UST, ustekinumab.