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Comparative Study
. 2014 May;12(5):811-817.e3.
doi: 10.1016/j.cgh.2013.06.010. Epub 2013 Jun 28.

Comparative effectiveness of infliximab and adalimumab for Crohn's disease

Affiliations
Comparative Study

Comparative effectiveness of infliximab and adalimumab for Crohn's disease

Mark T Osterman et al. Clin Gastroenterol Hepatol. 2014 May.

Abstract

Background & aims: Antibodies against tumor necrosis factor-α are widely used to treat patients with Crohn's disease (CD). This study compared the effectiveness of infliximab and adalimumab, the 2 most commonly used anti-tumor necrosis factor agents, in patients with CD.

Methods: We conducted a retrospective cohort study by using U.S. Medicare data from 2006 through 2010. Patients with CD who were new users of infliximab (n = 1459) or adalimumab (n = 871) after January 31, 2007, were included. Patients older than age 85 and those with rheumatoid arthritis, psoriasis, psoriatic arthritis, or ankylosing spondylitis were excluded. The primary outcome measures were disease persistence on therapy at week 26, surgery (including bowel resection, creation of an ostomy, or surgical treatment of a perforation or abscess), and hospitalization for CD. Propensity score-adjusted logistic and Cox regression were used to compute adjusted odds ratios or hazard ratios and 95% confidence intervals (CIs).

Results: After 26 weeks of treatment, 49% of patients receiving infliximab remained on drug, compared with 47% of those receiving adalimumab (odds ratio, 0.98; 95% CI, 0.81-1.19). Fewer patients treated with infliximab underwent surgery than those treated with adalimumab, but this difference was not statistically significant (5.5 vs 6.9 surgeries per 100 person-years; hazard ratio, 0.79; 95% CI, 0.60-1.05). Rates of hospitalization did not differ between groups (hazard ratio, 0.88; 95% CI, 0.72-1.07).

Conclusions: We observed similar effectiveness of infliximab and adalimumab for CD on the basis of 3 clinically important outcome measures.

Keywords: Hospitalization; Persistence; Surgery; Tumor Necrosis Factor-α.

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Conflict of interest statement

Potential conflicts of interest:

Dr. Osterman has served on advisory boards for Janssen, Abbott, and UCB. He has received research funding from UCB.

Dr. Delzell has received research support from Amgen.

Dr. Zhang has received research support from Genentech and Amgen.

Dr. Bewtra has received research support from Centocor.

Dr. Curtis has received honoraria for consulting from Roche/Genentech, UCB, Janssen, CORRONA, Amgen, Pfizer, BMS, Crescendo and AbbVie. He has received research support from Research: Roche/Genentech, UCB, Janssen, CORRONA, Amgen, Pfizer, BMS, CrescendoAbbVie.

Dr. Lewis has served as a consultant to Amgen, Millennium Pharmaceuticals, Pfizer, Abbott, Prometheus, Nestle, Lilly, and Shire. He has received research funding from Shire, Takeda, and Centocor.

The following authors report no potential conflict of interest: Dr. Haynes, Dr. Chen, Ms. Brensinger, Mr. Xie

Comment in

  • Infliximab vs adalimumab for Crohn's disease: perhaps too early to call it a tie.
    Dassopoulos T, Sorrentino D. Dassopoulos T, et al. Clin Gastroenterol Hepatol. 2014 May;12(5):818-20. doi: 10.1016/j.cgh.2013.12.006. Epub 2013 Dec 14. Clin Gastroenterol Hepatol. 2014. PMID: 24342747 No abstract available.
  • Infliximab vs adalimumab for Crohn's disease.
    Dhillon AS, Harris AW. Dhillon AS, et al. Clin Gastroenterol Hepatol. 2015 Jan;13(1):210. doi: 10.1016/j.cgh.2014.06.012. Epub 2014 Jun 19. Clin Gastroenterol Hepatol. 2015. PMID: 24954114 No abstract available.
  • Reply: To PMID 23811254.
    Osterman MT. Osterman MT. Clin Gastroenterol Hepatol. 2015 Jan;13(1):210-1. doi: 10.1016/j.cgh.2014.08.019. Epub 2014 Aug 20. Clin Gastroenterol Hepatol. 2015. PMID: 25151256 No abstract available.

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