Literature DB >> 32109956

Real-World Budget Impact of Listing a Biosimilar of Rituximab.

Arnaud Boidart1, Martin Darveau2, Nicole Déry2, Marie-Claude Racine2.   

Abstract

BACKGROUND: The approval of new biosimilars by national health agencies is expected to generate significant cost savings for health care systems. This is particularly the case with the biosimilar of rituximab approved for the Canadian market in 2019. However, several uncertainties remain regarding utilization of this agent.
OBJECTIVES: To determine the proportion of total annual drug expenses for each indication for rituximab in the hospital setting and to determine potential savings related to introduction of a biosimilar.
METHODS: A budget impact analysis was performed through 3 real-world scenarios, based on data obtained from a large university teaching hospital for a 12-month period.
RESULTS: This study involved data for 420 patients. Annual expenses for rituximab for all indications represented 7.7% of total annual drug spending for the hospital, of which 5.0% was related specifically to indications approved by Health Canada. More than 6% of the annual drug expenses was attributable to the use of rituximab for oncologic indications, including 1.8% for uses not approved by Health Canada. Overall, each 10% reduction in the price of a biosimilar of rituximab (relative to the reference rituximab) would result in annual savings of about 0.8% of total drug expenses in the hospital if a biosimilar was used for all real-world indications, whether approved by Health Canada or not.
CONCLUSIONS: The introduction of a biosimilar of rituximab to the Canadian market would generate significant savings. To properly assess the potential savings that this agent could generate in the limited budget environment of a hospital, it seems important to consider all of the indications for which it could be used. 2020 Canadian Society of Hospital Pharmacists. All content in the Canadian Journal of Hospital Pharmacy is copyrighted by the Canadian Society of Hospital Pharmacy. In submitting their manuscripts, the authors transfer, assign, and otherwise convey all copyright ownership to CSHP.

Entities:  

Keywords:  biosimilar; budget impact analysis; hospital setting; real-world analysis; rituximab

Year:  2020        PMID: 32109956      PMCID: PMC7023921     

Source DB:  PubMed          Journal:  Can J Hosp Pharm        ISSN: 0008-4123


  18 in total

1.  A pilot randomized trial of adjuvant rituximab or placebo for nonsplenectomized patients with immune thrombocytopenia.

Authors:  Donald M Arnold; Nancy M Heddle; Julie Carruthers; Deborah J Cook; Mark A Crowther; Ralph M Meyer; Yang Liu; Richard J Cook; Anne McLeod; Janet A MacEachern; Joy Mangel; David Anderson; Linda Vickars; Alan Tinmouth; Andre C Schuh; John G Kelton
Journal:  Blood       Date:  2012-01-05       Impact factor: 22.113

Review 2.  Current treatment strategies in autoimmune hemolytic disorders.

Authors:  Wilma Barcellini
Journal:  Expert Rev Hematol       Date:  2015-07-31       Impact factor: 2.929

3.  Rituximab as second-line treatment for adult immune thrombocytopenia (the RITP trial): a multicentre, randomised, double-blind, placebo-controlled trial.

Authors:  Waleed Ghanima; Abderrahim Khelif; Anders Waage; Marc Michel; Geir E Tjønnfjord; Neila Ben Romdhan; Johannes Kahrs; Bernadette Darne; Pål Andrè Holme
Journal:  Lancet       Date:  2015-02-05       Impact factor: 79.321

Review 4.  Frequency of the off-label use of monoclonal antibodies in clinical practice: a systematic review of the literature.

Authors:  Angeliki Zarkali; Drosos E Karageorgopoulos; Petros I Rafailidis; Matthew E Falagas
Journal:  Curr Med Res Opin       Date:  2013-11-12       Impact factor: 2.580

5.  Bendamustine plus rituximab versus CHOP plus rituximab as first-line treatment for patients with indolent and mantle-cell lymphomas: an open-label, multicentre, randomised, phase 3 non-inferiority trial.

Authors:  Mathias J Rummel; Norbert Niederle; Georg Maschmeyer; G Andre Banat; Ulrich von Grünhagen; Christoph Losem; Dorothea Kofahl-Krause; Gerhard Heil; Manfred Welslau; Christina Balser; Ulrich Kaiser; Eckhart Weidmann; Heinz Dürk; Harald Ballo; Martina Stauch; Fritz Roller; Juergen Barth; Dieter Hoelzer; Axel Hinke; Wolfram Brugger
Journal:  Lancet       Date:  2013-02-20       Impact factor: 79.321

Review 6.  Biosimilars: Practical Considerations for Pharmacists.

Authors:  James G Stevenson; Robert Popovian; Ira Jacobs; Susan Hurst; Lesley G Shane
Journal:  Ann Pharmacother       Date:  2017-02-08       Impact factor: 3.154

Review 7.  Biosimilars: From Extrapolation into Off Label Use.

Authors:  Sizheng Zhao; Jagdish R Nair; Robert J Moots
Journal:  Curr Pharm Des       Date:  2017       Impact factor: 3.116

8.  Rituximab before splenectomy in adults with primary idiopathic thrombocytopenic purpura: a meta-analysis.

Authors:  Sophie Auger; Yohan Duny; Jean François Rossi; Philippe Quittet
Journal:  Br J Haematol       Date:  2012-05-22       Impact factor: 6.998

Review 9.  Rituximab for immunologic renal disease: What the nephrologist needs to know.

Authors:  Andreas Kronbichler; Martin Windpessl; Herwig Pieringer; David R W Jayne
Journal:  Autoimmun Rev       Date:  2017-04-13       Impact factor: 9.754

10.  Application of the FDA Biosimilar Extrapolation Framework to Make Off-Label Determinations.

Authors:  Edward Li; Ernesto Lobaina
Journal:  J Manag Care Spec Pharm       Date:  2017-12
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