TY - JOUR
T1 - The benefit of combination therapy depends on disease phenotype and duration in Crohn's disease
AU - Ananthakrishnan, A. N.
AU - Sakuraba, A.
AU - Barnes, E. L.
AU - Pekow, J.
AU - Raffals, L.
AU - Long, M. D.
AU - Sandler, R. S.
N1 - Funding Information:
Funding information This work was supported by the Leona M. and Harry B. Helmsley Charitable Trust. Ananthakrishnan is supported in part by a grant from the National Institutes of Health (K23 DK097142). Declaration of personal interests: Ananthakrishnan has served on scientific advisory boards for Abbvie, Takeda, and Merck. Pekow has received research grants from Takeda and Abbvie. Other co-authors have no relevant disclosures.
Publisher Copyright:
© 2017 John Wiley & Sons Ltd
PY - 2017/7
Y1 - 2017/7
N2 - Background: The impact of combination therapy on disease-related morbidity in patients with established Crohn's disease (CD) or ulcerative colitis (UC) remains to be well-defined. Aim: To examine the effect of combination therapy on disease outcomes in CD and UC. Methods: Using a multicenter prospective cohort, we classified CD and UC patients as being on monotherapy with anti-TNF or on combination with an immunomodulator. The primary outcome was a composite of new IBD-related surgery, hospitalisations, penetrating complications, need for corticosteroids or new biological at 1 year. Multivariable regression models adjusted for potential confounders. Results: We included 707 patients with CD (45% combination therapy) and 164 with UC (38% combination therapy). Combination therapy was not associated with reduction in the composite outcome in either CD (OR: 0.87, 95% CI: 0.63-1.22) or UC (OR: 1.45, 95% CI: 0.63-3.38). However, while no difference was noted in those with nonstricturing, nonpenetrating CD, a significant reduction in the likelihood of the outcome was seen in those with stricturing or penetrating CD (30% vs 39%, OR: 0.58, 95% CI: 0.37-0.90). A stronger effect was also observed in those with disease duration <5 years (OR: 0.35, 95% CI: 0.14-0.87) compared to those with a longer duration (OR: 0.75, 95% CI: 0.45-1.27). A similar reduction in occurrence of composite outcome was noted with infliximab and with other anti-TNF biologics. Conclusion: The benefit of combination immunomodulator-biological therapy is stronger in those with complicated Crohn's disease, particularly early on in their disease course.
AB - Background: The impact of combination therapy on disease-related morbidity in patients with established Crohn's disease (CD) or ulcerative colitis (UC) remains to be well-defined. Aim: To examine the effect of combination therapy on disease outcomes in CD and UC. Methods: Using a multicenter prospective cohort, we classified CD and UC patients as being on monotherapy with anti-TNF or on combination with an immunomodulator. The primary outcome was a composite of new IBD-related surgery, hospitalisations, penetrating complications, need for corticosteroids or new biological at 1 year. Multivariable regression models adjusted for potential confounders. Results: We included 707 patients with CD (45% combination therapy) and 164 with UC (38% combination therapy). Combination therapy was not associated with reduction in the composite outcome in either CD (OR: 0.87, 95% CI: 0.63-1.22) or UC (OR: 1.45, 95% CI: 0.63-3.38). However, while no difference was noted in those with nonstricturing, nonpenetrating CD, a significant reduction in the likelihood of the outcome was seen in those with stricturing or penetrating CD (30% vs 39%, OR: 0.58, 95% CI: 0.37-0.90). A stronger effect was also observed in those with disease duration <5 years (OR: 0.35, 95% CI: 0.14-0.87) compared to those with a longer duration (OR: 0.75, 95% CI: 0.45-1.27). A similar reduction in occurrence of composite outcome was noted with infliximab and with other anti-TNF biologics. Conclusion: The benefit of combination immunomodulator-biological therapy is stronger in those with complicated Crohn's disease, particularly early on in their disease course.
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U2 - 10.1111/apt.14125
DO - 10.1111/apt.14125
M3 - Article
C2 - 28470787
AN - SCOPUS:85018316478
SN - 0269-2813
VL - 46
SP - 162
EP - 168
JO - Alimentary Pharmacology and Therapeutics
JF - Alimentary Pharmacology and Therapeutics
IS - 2
ER -