Real-World Comparison of Reference Infliximab versus the Biosimilar Infliximab-abda in Inflammatory Bowel Disease

2020 Year in Review - Biosimilars

Data from a large, nationwide, observational cohort study demonstrate that switching from reference infliximab to biosimilar infliximab-abda in patients with inflammatory bowel disease was safe and efficacious compared with continuing reference infliximab.

Several biosimilars to approved biologic agents have been developed for the management of a variety of immune-mediated inflammatory disorders, such as moderate-to-severe inflammatory bowel disease (IBD), including both Crohn’s disease (CD) and ulcerative colitis (UC). A large, nationwide, prospective, observational cohort study was conducted to evaluate the efficacy and safety of biosimilars in patients with IBD who switched from reference infliximab to biosimilar infliximab-abda compared with those who continued reference infliximab; the results of this study were presented at the American College of Gastroenterology 2020 meeting.

The chart review identified eligible patients with CD or UC who had received ≥1 doses of either infliximab or infliximab-abda from 2018 to 2019 at the Cleveland Clinic. Eligible patients were randomized into 2 cohorts; the first cohort included patients authorized for a nonmedical switch from infliximab to infliximab-abda, and the second cohort included patients who continued on infliximab. Statistical analysis consisted of between-cohort comparisons using nonparametric testing for continuous variables and categorical variables (α ≤0.05).

A total of 359 patients were included in the analysis; of these, 99 patients were switched from infliximab to infliximab-abda and 101 continued infliximab therapy. In terms of baseline demographics, the mean age of the total cohort was 41.95 years, 49% were male, and 87% were white. A higher proportion of patients with CD were included than UC in both cohorts. No clinically significant differences were observed in the use of corticosteroid taper and maintenance, fecal calprotectin, infliximab concentrations, antibody levels, and hospital and emergency department admissions.

The results of the observational study demonstrated that nonmedical switch from reference infliximab to biosimilar infliximab-abda was safe and efficacious compared with continuing reference infliximab therapy in patients with IBD.

Reference
Padival R, et al. American College of Gastroenterology (ACG) 2020 Virtual Annual Scientific Meeting & Postgraduate Course. Abstract P1625.

Related Items

Beyond the Jargon: Explaining Biosimilars to Patients
By Sharon S. Gentry, MSN, RN, HON-ONN-CG, AOCN, CBCN
March 2025 Vol 16, No 3
As biosimilars increase in the care arena of cancer treatment, it is critical that patients be informed of this classification of treatment in a way that allows for shared decision-making.
Panel: Biosimilar Adoption Dependent on Various Stakeholder Economics
January 2022 Vol 13, No 1
Thirty-one biosimilar products have been approved by the FDA, 20 of which have been launched in the United States.
Comparative Efficacy and Safety of the Bevacizumab Biosimilar MIL60 versus Bevacizumab Reference in Patients with Advanced or Recurrent Nonsquamous NSCLC
2021 Year in Review - Biosimilars
The results of a randomized, double-blind phase 3 study established the equivalence of bevacizumab reference to its biosimilar MIL60 in terms of clinical efficacy, safety, population pharmacokinetics, and immunogenicity in patients with nonsquamous NSCLC.
Journal of Oncology Navigation & Survivorship
JONS

Subscribe Today!

To sign up for our print publication or e-newsletter, please enter your contact information below.

I'd like to receive:

  • First Name *
    Last Name *
     
    Profession or Role
    Primary Specialty or Disease State
    Country