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The Efficacy, Safety, and Persistence of Therapy after Non-Medical Switching from an Originator Adalimumab in Inflammatory Bowel Disease: Real-Life Experience from Two Tertiary Centres. | LitMetric

AI Article Synopsis

  • Over the past 20 years, there's been a rise in new treatments for inflammatory bowel disease (IBD), significantly increasing therapy costs, which raises concerns among healthcare stakeholders.
  • The study involved 53 IBD patients in Bucharest who were switched from the original biologic treatment to a biosimilar of Adalimumab to evaluate clinical outcomes and side effects after one year.
  • Results indicated no significant changes in disease markers like fecal calprotectin and C-reactive protein after the switch, suggesting that the biosimilar is as effective and safe as the original Adalimumab, with minimal side effects reported.

Article Abstract

During the last two decades, an increased number of molecules with multiple mechanisms of action have been approved for the treatment of inflammatory bowel disease (IBD), with a substantial increase in the costs related to therapy, which has become a concern for payers, regulators, and healthcare professionals. Biosimilars are biologic medical products that are highly structurally similar to their reference products; have no clinically meaningful differences in terms of immunogenicity, safety, or effectiveness; and are available at a lower price. This was an observational prospective study conducted in two IBD centres in Bucharest and included 53 patients, 27 male (M) and 26 female (F), diagnosed with IBD according to standard clinical, endoscopic, radiological, and histological criteria, who were non-medically switched at the indication of the National Insurance House to a biosimilar of Adalimumab. The aim was to determine the rates of clinical remission, adverse effects, and treatment persistence at one year. No significant differences were found in terms of the faecal calprotectin (FC) and C-reactive protein (CRP) levels 6 and 12 months after changing from the originator biologic treatment to a biosimilar. Only one patient required a change in their biological treatment following the clinical and biological loss of response. The main adverse effect reported by the patients was pain at the injection site. Of the 53 patients, only 2 reported pain at the injection site, and 1 patient reported experiencing abdominal pain and rectal bleeding immediately after the switch, but no recurrence was observed clinically or endoscopically. : This observational study is the first to be carried out in Romania that shows that, after a non-medical switch, biosimilars of Adalimumab are as efficient and safe as the originator Adalimumab in the clinical treatment of patients with IBD.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11510052PMC
http://dx.doi.org/10.3390/ph17101319DOI Listing

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