Literature DB >> 29667324

Estimation of cost savings between 2011 and 2014 attributed to infliximab biosimilar in the South Korean healthcare market: real-world evidence using a nationwide database.

Jiyoun Kim1, Dongmun Ha1, Inmyung Song1, Haesun Park1, Sang-Won Lee1, Eui-Kyung Lee1, Ju-Young Shin1.   

Abstract

AIM: The introduction of biosimilars is expected to reduce the cost of biologic drugs, but the actual cost savings have not yet been quantified in Korea. The aim of this study was to estimate the annual cost savings attributed to the introduction of infliximab biosimilar.
METHODS: We conducted a retrospective analysis using data from the Health Insurance Review and Assessment Service-National Patients Sample (HIRA-NPS) between 2011 and 2014. The study subjects were patients who were treated with infliximab, adalimumab or etanercept. We compared the drug costs before and after the introduction of infliximab biosimilar in December 2012 (2011-2012 and 2013-2014) to estimate the annual drug cost savings attributed to this and the number of patients who could additionally benefit from the biosimilar in 2013 and 2014.
RESULTS: A total of 10 986 prescriptions were identified: 2620 for infliximab. The cost savings were estimated at $262 270 for 133 patients in 2013 and $395 220 for 174 patients in 2014. Among the patients who underwent a 1-year maintenance course of infliximab therapy, the annual expenditure on infliximab was lower in 2014 than in 2011. If the cost savings were used to treat additional patients, 13.3%-38.6% more patients per year could be treated by indication.
CONCLUSION: The introduction of infliximab biosimilar reduced direct medical costs for both patients and the payer, which could then be used to increase patient access to biologic medicines. The entry of infliximab biosimilar could result in further reductions in healthcare costs.
© 2018 Asia Pacific League of Associations for Rheumatology and John Wiley & Sons Australia, Ltd.

Entities:  

Keywords:  HIRA-NPS; biosimilar; cost saving; infliximab

Mesh:

Substances:

Year:  2018        PMID: 29667324     DOI: 10.1111/1756-185X.13295

Source DB:  PubMed          Journal:  Int J Rheum Dis        ISSN: 1756-1841            Impact factor:   2.454


  3 in total

1.  Uptake of Biosimilars and Its Economic Implication for the Treatment of Patients with Rheumatoid Arthritis in Korea.

Authors:  Soo Kyung Cho; Sun Young Jung; Hyoungyoung Kim; Yeo Jin Song; Kyungeun Lee; Yoon Kyoung Sung
Journal:  J Korean Med Sci       Date:  2021-05-24       Impact factor: 2.153

2.  Long-term Efficacy, Safety, and Immunogenicity of the Infliximab (IFX) Biosimilar, PF-06438179/GP1111, in Patients with Rheumatoid Arthritis After Switching from Reference IFX or Continuing Biosimilar Therapy: Week 54-78 Data From a Randomized, Double-Blind, Phase III Trial.

Authors:  Stanley B Cohen; Sebastiao C Radominski; Hideto Kameda; Alan J Kivitz; Michael Tee; Carol Cronenberger; Min Zhang; Sarah Hackley; Muhammad I Rehman; Oliver von Richter; Rieke Alten
Journal:  BioDrugs       Date:  2020-04       Impact factor: 5.807

3.  Retention Rate and Safety of Biosimilar CT-P13 in Rheumatoid Arthritis: Data from the Korean College of Rheumatology Biologics Registry.

Authors:  Hyoun-Ah Kim; Eunyoung Lee; Sun-Kyung Lee; Yong-Beom Park; Young Nam Lee; Hee Jung Kang; Kichul Shin
Journal:  BioDrugs       Date:  2020-02       Impact factor: 5.807

  3 in total

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