Expanded access to cancer treatments from conversion to neutropenia prophylaxis with biosimilar filgrastim-sndz
Affiliation
Univ Arizona, Ctr Canc, Dept PharmUniv Arizona, Dept Pharm Practice & Sci, Coll Pharm
Univ Arizona, Ctr Hlth Outcomes & PharmacoEcon Res
Univ Arizona, Dept Family & Community Med, Coll Med
Issue Date
2017-10
Metadata
Show full item recordPublisher
FUTURE MEDICINE LTDCitation
Expanded access to cancer treatments from conversion to neutropenia prophylaxis with biosimilar filgrastim-sndz 2017, 13 (25):2285 Future OncologyJournal
Future OncologyRights
© Abraham. This work is licensed under the Attribution-NonCommercial-NoDerivatives 4.0 Unported License.Collection Information
This item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.Abstract
Aim: Biosimilar medicines offer significant cost-savings potential over their reference products, which can be re-allocated to provide access to other cancer treatments on a budget-neutral basis. Methods: Simulation study using cost data for the USA under consideration of several prophylaxis patterns. Results: Potential savings from conversion from reference filgrastim to biosimilar filgrastim-sndz are significant. These savings expand budget-neutral access to novel immunotherapies (obinutuzumab; pembrolizumab) or supportive care (filgrastim-sndz). Conclusion: The combination of biosimilar savings and expanded access increases the value of cancer care as the same supportive care is provided at lower cost, additional cancer care is enabled at no additional cost, and more patients will have access to cancer care.Note
Open access article.ISSN
1479-66941744-8301
PubMed ID
28870106Version
Final published versionSponsors
Sandoz Inc., Princeton, NJ, USAAdditional Links
http://www.futuremedicine.com/doi/10.2217/fon-2017-0374ae974a485f413a2113503eed53cd6c53
10.2217/fon-2017-0374
Scopus Count
Collections
Except where otherwise noted, this item's license is described as © Abraham. This work is licensed under the Attribution-NonCommercial-NoDerivatives 4.0 Unported License.
Related articles
- Economic modeling for the US of the cost-efficiency and associated expanded treatment access of conversion to biosimilar pegfilgrastim-bmez from reference pegfilgrastim.
- Authors: McBride A, Wang W, Campbell K, Balu S, MacDonald K, Abraham I
- Issue date: 2020 Aug
- Patient-Administered Biologic and Biosimilar Filgrastim May Offer More Affordable Options for Patients with Nonmyeloid Malignancies Receiving Chemotherapy in the United States: A Budget Impact Analysis from the Payer Perspective.
- Authors: Trautman H, Szabo E, James E, Tang B
- Issue date: 2019 Jan
- Potential cost savings from chemotherapy-induced febrile neutropenia with biosimilar filgrastim and expanded access to targeted antineoplastic treatment across the European Union G5 countries: a simulation study.
- Authors: Sun D, Andayani TM, Altyar A, MacDonald K, Abraham I
- Issue date: 2015 Apr 1
- Cost-efficiency analyses for the US of biosimilar filgrastim-sndz, reference filgrastim, pegfilgrastim, and pegfilgrastim with on-body injector in the prophylaxis of chemotherapy-induced (febrile) neutropenia.
- Authors: McBride A, Campbell K, Bikkina M, MacDonald K, Abraham I, Balu S
- Issue date: 2017 Oct
- Regulatory and Clinical Experiences with Biosimilar Filgrastim in the U.S., the European Union, Japan, and Canada.
- Authors: Chen B, Nagai S, Armitage JO, Witherspoon B, Nabhan C, Godwin AC, Yang YT, Kommalapati A, Tella SH, DeAngelis C, Raisch DW, Sartor O, Hrushesky WJ, Ray PS, Yarnold PR, Love BL, Norris LB, Knopf K, Bobolts L, Riente J, Luminari S, Kane RC, Hoque S, Bennett CL
- Issue date: 2019 Apr