» Articles » PMID: 36911254

Monitoring a Mandatory Nonmedical Switching Policy from Originator to Biosimilar Infliximab in Patients with Inflammatory Bowel Diseases: A Population-Based Cohort Study

Overview
Publisher Wiley
Specialty Gastroenterology
Date 2023 Mar 13
PMID 36911254
Authors
Affiliations
Soon will be listed here.
Abstract

Background: On September 5, 2019, British Columbia announced a new policy (the Biosimilars Initiative) to switch from originator to biosimilar infliximab for patients with inflammatory bowel diseases.

Objective: To monitor the impacts of the policy on the use of medications and health services during the first year of the policy.

Methods: In this population-based cohort study, we used administrative health data to construct three historical cohorts and one policy cohort of patients with inflammatory bowel diseases who used the originator infliximab. We then monitored the cumulative incidence of medications and health services. Log-likelihood ratios were used to quantify differences between the policy cohort and the average of the historical cohorts.

Results: The cohorts included 1839-2368 users of the originator infliximab, ages 4-90 years, mean age 43 years. During the first year of follow-up, we found: (1) a 0.9% increase in the first dispensation of infliximab, biosimilar, or originator; (2) a 16.2% increase in infliximab dose escalation; (3) a decrease of 2.4% in the dispensation of antibiotics and a 2.6% decrease in new use of prednison; (4) an anticipated increase in visits to physicians and gastroenterologists to manage switching to biosimilars (24.0%); (5) a 4.0% decrease in discharges from hospital; and (6) a 2.9% decrease in emergency admissions to hospital.

Conclusion: British Columbia's Biosimilars Initiative for nonmedical switching from originator to biosimilar infliximab for inflammatory bowel diseases was not associated with harmful impacts on medications and health services use. An increase in dose escalation was accompanied by an improvement in health status proxies.

Citing Articles

Incidence of serious infection among etanercept and infliximab initiators: safety comparison between biosimilars and bio-originators with Canadian population-based data.

Birck M, Lukusa L, Choquette D, Boire G, Maksymowych W, Singh H BMC Rheumatol. 2024; 8(1):47.

PMID: 39343928 PMC: 11441163. DOI: 10.1186/s41927-024-00415-5.

References
1.
van Hoeve K, Dreesen E, Hoffman I, Van Assche G, Ferrante M, Gils A . Efficacy, Pharmacokinetics, and Immunogenicity is Not Affected by Switching From Infliximab Originator to a Biosimilar in Pediatric Patients With Inflammatory Bowel Disease. Ther Drug Monit. 2019; 41(3):317-324. DOI: 10.1097/FTD.0000000000000601. View

2.
Hughes A, Marshall J, Moretti M, Ungar W . A Cost-Utility Analysis of Switching from Reference to Biosimilar Infliximab Compared to Maintaining Reference Infliximab in Adult Patients with Crohn's Disease. J Can Assoc Gastroenterol. 2021; 4(1):48. PMC: 7898373. DOI: 10.1093/jcag/gwz045. View

3.
Convertino I, Lucenteforte E, Gini R, Lorenzoni V, Cazzato M, Turchetti G . Utilisation patterns and clinical impact of the introduction of infliximab-biosimilar in Tuscany, Italy: real world evidence following the recommendation of switching for non-medical reasons. Clin Exp Rheumatol. 2020; 39(4):753-762. View

4.
Karlsson P, Nakitanda A, Lofling L, Cesta C . Patterns of prescription dispensation and over-the-counter medication sales in Sweden during the COVID-19 pandemic. PLoS One. 2021; 16(8):e0253944. PMC: 8362980. DOI: 10.1371/journal.pone.0253944. View

5.
Moayyedi P, Benchimol E, Armstrong D, Yuan C, Fernandes A, Leontiadis G . Joint Canadian Association of Gastroenterology and Crohn's Colitis Canada Position Statement on Biosimilars for the Treatment of Inflammatory Bowel Disease. J Can Assoc Gastroenterol. 2020; 3(1):e1-e9. PMC: 6985688. DOI: 10.1093/jcag/gwz035. View