TY - JOUR
T1 - Systematic review and meta-analysis
T2 - Infliximab or cyclosporine as rescue therapy in patients with severe ulcerative colitis refractory to steroids
AU - Narula, Neeraj
AU - Marshall, John K.
AU - Colombel, Jean Frederic
AU - Leontiadis, Grigorios I.
AU - Williams, John G.
AU - Muqtadir, Zack
AU - Reinisch, Walter
N1 - Publisher Copyright:
© 2016 by the American College of Gastroenterology.
PY - 2016/4/1
Y1 - 2016/4/1
N2 - OBJECTIVES:Acute severe steroid-refractory ulcerative colitis (UC) carries a poor prognosis and requires optimal management. A systematic review and meta-analysis were conducted to assess cyclosporine and infliximab (IFX) as rescue agents in patients with steroid-refractory UC.METHODS:A literature search identified studies that investigated IFX and cyclosporine in steroid-refractory UC patients. The primary outcome was short-term response to treatment. Secondary outcomes included the rates of colectomy at 3 months and 12 months, adverse drug reactions, post-operative complications in those who received rescue therapy but underwent colectomy subsequently, and mortality. Odds ratios (ORs) with 95% confidence intervals (CIs) are reported.RESULTS:Overall, 16 studies with 1,473 participants were eligible for inclusion. Among three randomized controlled trials, no significant difference was seen with IFX compared with cyclosporine with regard to treatment response and 3- or 12-month colectomy. Among 13 non-randomized studies, IFX was associated with significantly higher rates of treatment response (OR 2.96 (95% CI 2.12-4.14, χ 2 =6.50, I 2 =0%)) and a lower 12-month colectomy rate (OR 0.42 (95% CI 0.22-0.83, χ 2 =30.94, I 2 =71%)), with no significant difference seen in the 3-month colectomy rate (OR 0.53 (95% CI 0.22-1.28, χ 2 =22.73, I 2 =69%)) compared with cyclosporine. There were no significant differences between IFX and cyclosporine in adverse drug-related events, post-operative complications, or mortality.CONCLUSIONS:In the management of steroid-refractory severe UC, no definitive difference between IFX and cyclosporine is demonstrated by randomized trials, but non-randomized studies suggest that IFX is associated with better treatment response and lower risk of colectomy at 12 months. Prospective studies comparing dose-optimized IFX with cyclosporine are needed.
AB - OBJECTIVES:Acute severe steroid-refractory ulcerative colitis (UC) carries a poor prognosis and requires optimal management. A systematic review and meta-analysis were conducted to assess cyclosporine and infliximab (IFX) as rescue agents in patients with steroid-refractory UC.METHODS:A literature search identified studies that investigated IFX and cyclosporine in steroid-refractory UC patients. The primary outcome was short-term response to treatment. Secondary outcomes included the rates of colectomy at 3 months and 12 months, adverse drug reactions, post-operative complications in those who received rescue therapy but underwent colectomy subsequently, and mortality. Odds ratios (ORs) with 95% confidence intervals (CIs) are reported.RESULTS:Overall, 16 studies with 1,473 participants were eligible for inclusion. Among three randomized controlled trials, no significant difference was seen with IFX compared with cyclosporine with regard to treatment response and 3- or 12-month colectomy. Among 13 non-randomized studies, IFX was associated with significantly higher rates of treatment response (OR 2.96 (95% CI 2.12-4.14, χ 2 =6.50, I 2 =0%)) and a lower 12-month colectomy rate (OR 0.42 (95% CI 0.22-0.83, χ 2 =30.94, I 2 =71%)), with no significant difference seen in the 3-month colectomy rate (OR 0.53 (95% CI 0.22-1.28, χ 2 =22.73, I 2 =69%)) compared with cyclosporine. There were no significant differences between IFX and cyclosporine in adverse drug-related events, post-operative complications, or mortality.CONCLUSIONS:In the management of steroid-refractory severe UC, no definitive difference between IFX and cyclosporine is demonstrated by randomized trials, but non-randomized studies suggest that IFX is associated with better treatment response and lower risk of colectomy at 12 months. Prospective studies comparing dose-optimized IFX with cyclosporine are needed.
UR - http://www.scopus.com/inward/record.url?scp=84957812490&partnerID=8YFLogxK
U2 - 10.1038/ajg.2016.7
DO - 10.1038/ajg.2016.7
M3 - Review article
C2 - 26856754
AN - SCOPUS:84957812490
SN - 0002-9270
VL - 111
SP - 477
EP - 491
JO - American Journal of Gastroenterology
JF - American Journal of Gastroenterology
IS - 4
ER -