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Outcome of adult patients with JIA treated with the biosimilar BenepaliĀ®: results of the biologic register JuMBO

Authors :
Vollbach, Kristina
Tenbrock, Klaus
Wagner, Nobert
Horneff, Gerd
Klein, Ariane
Foeldvari, Ivan
Haas, Johannes-Peter
Aries, Peer
Gauler, Georg
Striesow, Frank
Hoff, Paula
Scholz, Christine
Tatsis, Stefanie
Seipelt, Eva
Klotsche, Jens
Minden, Kirsten
Source :
Arthritis Research & Therapy (formerly Arthritis Research); December 2022, Vol. 24 Issue: 1
Publication Year :
2022

Abstract

Background: To analyze therapy adherence, safety, and outcome in adult patients with juvenile idiopathic arthritis (JIA) treated with the etanercept biosimilar Benepali<superscript>®</superscript>(Biogen Inc, Cambridge, USA). Methods: Data from the prospective registry, JuMBO (Juvenile arthritis MTX/Biologics long-term Observation), were used for the analysis. JuMBO is a long-term observational cohort study. It follows adult patients with JIA who were formerly included in the national JIA biologic register (BiKeR Registry). Both registries provide individual trajectories of clinical data and outcomes from childhood to adulthood in JIA patients treated with disease-modifying anti-rheumatic drugs (DMARDs). Results: Eighty-three patients from the German JuMBO registry were treated with Benepali<superscript>®</superscript>. Of these, 74% had switched from Enbrel<superscript>®</superscript>(Pfizer Inc., NYC, USA) the originator of etanercept to Benepali<superscript>®</superscript>for cost reasons. Therapy survival of patients treated with Benepali<superscript>®</superscript>in comparison to Enbrel<superscript>®</superscript>in patients matched by significant parameters was comparable. Adverse events (AE) were reported in 25.3% and serious adverse events (SAE) in 9.6% of patients. Physicians rated no SAE causative related to Benepali<superscript>®</superscript>. The majority of SAEs were surgical/medical procedures and there was only one infection. All efficacy parameters (cJADAS-10, Physician Global Assessment, number of joints with active arthritis, patientsā€™ overall well-being, pain, and HAQ) demonstrated improvement over 24 months (p-values were not significant). 9.6% of patients permanently discontinued Benepali® because of an AE. Conclusions: Tolerability and effectiveness of the biosimilar Benepali<superscript>®</superscript>were satisfactory and therapy survival was comparable to the originator. Further data on therapy with biologics and biosimilars such as Benepali<superscript>®</superscript>must be collected by registries such as BiKeR and JuMBO in order to optimize therapy and patient outcomes and to reduce costs in the health system in the long term.

Details

Language :
English
ISSN :
14786354 and 14786362
Volume :
24
Issue :
1
Database :
Supplemental Index
Journal :
Arthritis Research & Therapy (formerly Arthritis Research)
Publication Type :
Periodical
Accession number :
ejs61413382
Full Text :
https://doi.org/10.1186/s13075-022-02968-7