Skip to main content
. 2024 Jan 5;17:17562848231221713. doi: 10.1177/17562848231221713

Table 3.

Univariate analysis of factors associated with clinical response and remission with the second anti-TNF in the whole cohort (N = 473).

Variable Response at week 14 p Remission at week 52 p
No Yes No Yes
Female gender 46% 49% 0.518 47.9% 45.9% 0.764
Never smoker 65.7% 63% 0.752 65.7% 62.1% 0.719
Extensive colitis 58.6% 59.5% 0.851 59.9% 57.4% 1
Age at first anti-TNF, median (range interval) 42 (20) 42 (22) 0.815 42 (20) 44 (21) 0.438
Disease duration at the beginning of the first anti-TNF, median (range interval) 43 (89) 49.5 (91) 0.661 45 (87) 47 (106) 0.872
Concomitant immunosuppressant with first anti-TNF 58.6% 49.5% 0.052 54.7% 50.7% 0.425
Dose escalation of first anti-TNF 46% 38.6% 0.112 47.9% 32.4% <0.001
Cause for discontinuation of first anti-TNF <0.001 <0.001
 Secondary loss of response 34.6% 38.1% 37.5% 33.1%
 Primary partial/nonresponse 41.8% 25.7% 39.2% 25.7%
 Adverse effect 20.2% 27.1% 19.1% 31.1%
Time on the first anti-TNF, median (range interval) 28.1 (45.9) 40.1 (75.6) 0.038 30.7 (55) 36.3 (76) 0.649
Disease duration at the beginning of the second anti-TNF, median (range interval) 60 (98) 76.5 (108) 0.491 62 (100) 78 (116) 0.463
Concomitant immunosuppressant with second anti-TNF 54.4% 49.5% 0.309 51.8% 50.7% 0.842
Moderate-to-severe partial Mayo score at the beginning of the second anti-TNF 66% 63.3% 0.622 69.8% 54.3% <0.001
Moderate-to-severe Mayo endoscopic subscore at the beginning of the second anti-TNF 89.7% 84.4% 0.226 87.6% 85.7% 0.709

Bold and italic characters within the Tables are used to highlight statistically significant results.