Comparison of medical costs among patients using adalimumab and infliximab: a retrospective study (COMPAIRS)

Daniel A Sussman1, Nisa Kubiliun, Parvez M Mulani

  • 1University of Miami, Division of Gastroenterology, Miami, Florida 33136, USA. dsussman@med.miami.edu

Insights

Adalimumab (ADA) therapy resulted in lower healthcare costs for Crohn's disease (CD) patients compared to infliximab (IFX). This cost difference was primarily driven by reduced outpatient medical expenses in the ADA group.

Area of Science:

  • Gastroenterology
  • Health Economics
  • Pharmacoeconomics

Background:

  • Anti-tumor necrosis factor (TNF) therapies are crucial for Crohn's disease (CD) management.
  • Real-world comparative data on the costs and utilization of adalimumab (ADA) and infliximab (IFX) in CD is limited.
  • This study addresses the need for comparative real-world evidence on anti-TNF medications in CD.

Purpose of the Study:

  • To compare the direct healthcare costs and utilization of ADA versus IFX in patients with CD initiating anti-TNF therapy.
  • To identify drivers of cost differences between ADA and IFX in a real-world setting.

Main Methods:

  • Retrospective analysis of insurance claims data (MarketScan database) for CD patients initiating ADA or IFX.
  • Propensity score matching was used to create comparable ADA and IFX cohorts (n=623 each).
  • Primary endpoint: direct healthcare costs within 6 months post-initiation. Secondary endpoints: healthcare utilization patterns.

Main Results:

  • Propensity-matched cohorts exhibited similar baseline characteristics.
  • Total 6-month healthcare costs were significantly lower for ADA ($18,885) compared to IFX ($24,355), a difference of $5,470 (P < 0.0001).
  • CD-related costs were also significantly lower with ADA ($16,454) vs. IFX ($22,316) (P < 0.0001), largely due to reduced outpatient visit costs.

Conclusions:

  • Adalimumab (ADA) is associated with lower 6-month healthcare costs compared to infliximab (IFX) in Crohn's disease patients.
  • The cost savings with ADA were partly attributed to lower outpatient medical expenditures.
  • Findings provide valuable real-world economic insights for anti-TNF treatment decisions in CD.
Abstract

Related Concept Videos

Drugs for Treatment of Crohn's Disease in IBD Using Biologic Agents: Anti-TNF01:24

Drugs for Treatment of Crohn's Disease in IBD Using Biologic Agents: Anti-TNF

Tumor Necrosis Factor (TNF), a proinflammatory cytokine, contributes significantly to the inflammation seen in Crohn's disease. It exists as soluble TNF and membrane-bound TNF, with actions mediated through TNF receptors (TNFR). TNFR activation leads to the release of proinflammatory cytokines, T-cell activation, collagen production, and leukocyte migration, all contributing to inflammation in Crohn's disease. Anti-TNF monoclonal antibodies, namely infliximab (Remicade), adalimumab (Humira),...
Drugs for Treatment of Crohn's Disease in IBD Using Immunomodulatory Agents01:29

Drugs for Treatment of Crohn's Disease in IBD Using Immunomodulatory Agents

Crohn's disease is an inflammatory bowel disorder marked by chronic inflammation of the GI tract. Various treatment strategies for Crohn's disease are employed, such as immunomodulatory agents, glucocorticoids, and biologics or anti-TNF therapy. Azathioprine (Imuran), a commonly used immunomodulatory drug for Crohn's disease, is converted in the body to mercaptopurine, which inhibits purine biosynthesis and cell proliferation. Both are utilized in severe cases of Inflammatory Bowel Disease...
Drug Products: Biologics, Biosimilars and Interchangeables01:28

Drug Products: Biologics, Biosimilars and Interchangeables

Biologics, derived from living sources such as humans, animals, or microorganisms, represent a significant category of pharmaceuticals. These complex molecules, developed through advanced biotechnological methods or purified from natural sources, include essential medical treatments like insulin and growth hormones. The complexity of biologics arises from their large molecular structures and the intricate processes required for their production, making them distinct from conventional...
Bioequivalence of Drugs: Drugs with Multiple Indications01:09

Bioequivalence of Drugs: Drugs with Multiple Indications

The concept of therapeutic equivalence (TE) in drugs with multiple indications is complex. A generic drug may be therapeutically equivalent to a brand-name product for one specific indication, but this doesn't necessarily mean it's equivalent for all other indications. Evidence of TE in one patient group and bioequivalence shown in healthy volunteers can support—but not confirm—TE for other indications. However, definitive proof requires individual clinical studies for each indication due to...
Types of Biopharmaceutical Studies: Controlled and Non-Controlled Approaches01:23

Types of Biopharmaceutical Studies: Controlled and Non-Controlled Approaches

Biopharmaceutical studies constitute a vital field aiming to enhance drug delivery methods and refine therapeutic approaches, drawing upon diverse interdisciplinary knowledge. In research methodologies, the choice between controlled and non-controlled studies significantly influences the study's reliability and accuracy.
Non-controlled studies, commonly employed for initial exploration, lack a control group, rendering them susceptible to biases and external influences. In contrast, controlled...
Pharmaceutical Alternatives: Stability-Related Therapeutic Nonequivalence01:22

Pharmaceutical Alternatives: Stability-Related Therapeutic Nonequivalence

Generic intravenous (IV) drugs are considered bioequivalent to their branded counterparts due to their 100% bioavailability upon administration. However, variations in stability among different drug products can significantly influence their therapeutic performance, even if they are pharmaceutically equivalent.Cefuroxime, a prophylactic antimicrobial, is often used as a single-dose IV injection for patients undergoing coronary artery bypass grafting surgery. A 3 g dose typically provides...