A propensity score-weighted comparison between adalimumab originator and its biosimilars, ABP501 and SB5, in inflammatory bowel disease: a multicenter Italian study

Author:

Barberio Brigida1ORCID,Cingolani Linda1,Canova Cristina2,Barbieri Giulia2,Sablich Renato3,Urbano Maria Teresa3,Bertani Lorenzo4ORCID,Costa Francesco4,Bodini Giorgia5ORCID,Demarzo Maria Giulia5,Ferronato Antonio6,Buda Andrea7,Melatti Piera1,Massimi Davide1,Savarino Edoardo Vincenzo8ORCID,Zingone Fabiana1ORCID

Affiliation:

1. Department of Surgery, Oncology, Gastroenterology, University of Padua, Padua, Veneto, Italy

2. Department of Cardio-Thoraco-Vascular Sciences and Public Health, University of Padua, Padua, Italy

3. Gastroenterology Unit, Santa Maria degli Angeli Hospital, Pordenone, Friuli-Venezia Giulia, Italy

4. Department of Translational Research and New Technologies in Medicine and Surgery, University of Pisa, Pisa, Italy

5. Gastroenterology Unit, Department of Internal Medicine, University of Genoa, IRCCS Ospedale Policlinico San Martino, University of Genoa, Genoa, Italy

6. Endoscopy Unit, Alto Vicentino Hospital, AULSS7 Pedemontana, Santorso, Veneto, Italy

7. Gastroenterology Unit, Hospital Feltre, Italy

8. Division of Gastroenterology, Department of Surgery, Oncology and Gastroenterology, University of Padua, Via Giustiniani 2, Padua, 35128, Italy

Abstract

Background: Adalimumab is an effective and safe biological drug for the treatment of inflammatory bowel disease (IBD). Nowadays, several biosimilar agents are available, but data regarding their efficacy and safety in patients with IBD are still lacking. We aimed to compare the effectiveness and tolerability between adalimumab originator, ABP501 and SB5 biosimilars in patients with IBD in the short term (after induction and after 6 months of treatment) through a propensity score-weighted multicenter cohort study. Methods: We included 156 patients with IBD, 69 patients with ulcerative colitis and 87 patients with Crohn’s disease (CD) receiving ABP501 or SB5 biosimilars from January 2019 to April 2020 for moderate-to-severe disease. For comparison, a group of age- and sex-matched patients treated with adalimumab originator was used. We collected clinical and biochemical data after induction and at 6 months of treatment. Endoscopic data were recorded only at baseline. Results: Overall, clinical benefit was achieved by 86.4% and 85.3% after induction and at 6 months, respectively, without a statistically significant difference between the three treatment groups ( p = 0.68 and p = 0.46). However, after induction, we found significant differences between the two types of the disease (ulcerative colitis or CD, p = 0.004), with a greater clinical benefit achieved by patients with CD. Also, the therapeutic optimization rate between the three drugs was not statistically significant different ( p = 0.30). All treatments showed a good safety profile, with only 10 patients who needed to stop therapy because of adverse events. Conclusion: Adalimumab biosimilars seem to be as effective and safe as the originator in patients with IBD. Surely, they represent a great opportunity to reduce the costs of biological therapies, however larger and longer real-life studies are necessary.

Publisher

SAGE Publications

Subject

Gastroenterology

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