Enteral Nutrition |
Clinical remission (PCDAI) |
65 (pediatric) |
Colonic: 50% |
(13) |
Ileocolonic: 82% |
Ileal: 92% |
Enteral Nutrition |
Clinical remission (CDAI <150) |
241 |
Colonic: 52% |
(15) |
Non-isolated colonic: 68% |
Metronidazole |
Improvement (CDAI) |
63 |
Small intestine +86 (38–134) (n = 24) |
(16) |
Small/large intestine +60 (19–101) (n = 31) |
Large intestine + 145 (26–265) (n = 8) |
Budesonide, Ciprofloxacin, Metronidazole |
Clinical remission (CDAI <150) |
80 |
Ileocolonic: 53% |
(17) |
Ileal: 26% |
Certolizumab pegol (CZP) |
Likeliness to achieve clinical remission (CDAI <150) at week 6 |
438 |
Colonic: OR 2.39 vs. placebo (95% CI 0.99–5.75, p = 0.052) |
(26) |
Ileocolonic: OR 2.07 (95% CI 1.01–4.28, p = 0.048) |
Ileal: OR 0.42 (95% CI 0.18–0.99, p = 0.048) |
Infliximab |
Clinical response (HBI reduction by > 3) at week 4 |
37 |
Colonic: 88% |
(27) |
Ileal: 54% |
(p = 0.042, OR 3.83) |
Infliximab |
Clinical response at week 8 (reduction of CDAI by ≥ 100) |
44 |
Colonic: 83.3% |
(28) |
Ileal/ileocolonic: 50% |
(p = 0.03) |
Infliximab |
Response at week 4 (reduction CDAI ≥70) or week 10 (50% decrease in draining fistulae) |
240 |
Colonic: 81% |
(29) |
Ileocolonic: 74% |
Ileal: 55% |
OR 1.905 (95% CI 1.010–3.597) |
Infliximab |
Loss of response |
284 (pediatric) |
Colonic: HR 2.72 (95% CI 1.30–5.71, p = 0.008) |
(30) |
Adalimumab |
Dose escalation (weeks) |
75 |
Colonic: 13.2 |
(31) |
Other sites: 34.6 |
P = 0.0062 |
Ustekinumab (UST) |
Clinical response or remission (CDAI) |
306 |
Ileal: 33.5% |
(5) |
Colonic: 49.2% |
Relative risk 0.68 (95% CI, 0.50–0.92) |
Vedolizumab (VDZ) |
Clinical response or remission (CDAI) |
155 |
Ileal: 21.2% |
(35) |
Colonic: 22.4% |
Relative risk 0.82 (95% CI, 0.42–1.60) |
Meat-analysis RCTs (CZP, UST, VDZ) |
Clinical response or remission (CDAI) |
288 |
Ileal: 29% |
(5) |
Colonic: 38% |
Relative risk 0.70 (95% CI, 0.56–0.87; I2 ¼ 0%) |
Vedolizumab |
Clinical remission (CDAI <150) at week 52 |
168 |
Colonic VDZ: 49.1% |
(36) |
Colonic placebo: 23.1% of Estimate 26.0 (95% CI, 5.1–46.9) |
Ileal VDZ: 36.4% |
Ileal Placebo: 42.9% |
Estimate −6.5 (95% CI, −30.6-17.6) |
Ustekinumab |
Loss of steroid-free clinical response (CDAI) |
104 |
Colonic: aHR 0.33 (0.11–0.98) Ileocolonic: aHR 0.26 (0.10–0.68) |
(37) |
Ustekinumab |
Clinical response (CDAI) |
152 |
Colonic: OR, 3.5 (95% CI: 1.34–9.41) |
(38) |
Ustekinumab |
Clinical response (CDAI) at week 26 |
407 |
Colonic: OR, 0.56 (95% CI, 0.32–0.96) |
(39) |
Ileocolonic: OR, 0.34 (95% CI, 0.16–0.69) |
Adalimumab |
Mean change (CDEIS); Global Histologic Disease Activity Scores |
70 |
Rectum-transverse colon: |
(41) |
−68.5% to −90.6% CDEIS |
Right colon-ileum: −22.3% to −50.0% CDEIS |
Colonic: 28.3% GHDAS healing Ileum: 21.2% GHDAS healing |
Anti-TNF |
Endoscopic healing (SES-CD) ≤ 5) at a median of 13 months |
156 |
Colonic: 79% |
(42) |
Small bowel: 36% |
SONIC-study |
Endoscopic remission (ER) at week 26 (CDEIS, SES-CD) |
172 |
ER rate of ileal ulcers significantly lower than colonic ulcers (P < 0.0001) |
(44) |
TAILORIX-study |
Endoscopic remission (CDEIS <3) at week 12 and 54 |
122 |
Lower ER rates in the ileum vs. colonic segments (P < 0.01 all comparisons) |
(45) |
Infliximab |
Mucosal healing (SES-CD: 0) and SES-CD change at week 30/38 |
101 |
MH transverse colon: 81% |
(46) |
MH ileum: 45% |
SES-CD change (week 30/38) transverse colon: −94%/-94% |
SES-CD change (week 30/38) ileum: 67%/69% |
Vedolizumab |
Mucosal healing (absence of any ulcers, including aphthae) at week 26 |
101 |
Rectum 38.5%; descending colon 31.7%; transverse colon 51%; ascending colon 46.1%; ileum 20.6% |
(47) |