Literature DB >> 36266557

Cost-effectiveness Analysis of Tisagenlecleucel Versus Blinatumomab in Children and Young Adults with Acute Lymphoblastic Leukemia: Partitioned Survival Model to Assess the Impact of an Outcome-Based Payment Arrangement.

Amy Gye1, Stephen Goodall2, Richard De Abreu Lourenco2.   

Abstract

OBJECTIVE: This research assesses the impact of an outcome-based payment arrangement (OBA) linking complete remission (CR) to survival as a means of maintaining cost-effectiveness for a chimeric antigen receptor T cell (CAR-T) therapy in young patients with acute lymphoblastic leukemia (ALL).
METHODS: A partitioned survival model (PSM) was used to model the cost-effectiveness of tisagenlecleucel versus blinatumomab in ALL from the Australian healthcare system perspective. A decision tree modeled different OBAs by funneling patients into a series of PSMs based on response. Outcomes were informed by individual patient data, while costs followed Australian treatment practices. Costs and quality-adjusted life years (QALYs) were combined to calculate a single incremental cost-effectiveness ratio (ICER), reported in US dollars (2022) at a discount rate of 5% on costs and outcomes.
RESULTS: For the base case, incremental costs and benefit were $379,595 and 4.27 QALYs, giving an ICER of $88,979. The ICER was most sensitive to discount rate ($57,660-$75,081), "cure point" ($62,718-$116,206) and extrapolation method ($76,018-$94,049). OBAs had a modest effect on the ICER when response rates varied. A responder-only payment was the most effective arrangement for maintaining the ICER ($88,249-$89,434), although this option was associated with the greatest financial uncertainty. A split payment arrangement (payment on infusion followed by payment on response) reduced variability in the ICER ($82,650-$99,154) compared with a single, upfront payment ($77,599-$107,273).
CONCLUSION: OBAs had a modest impact on reducing cost-effectiveness uncertainty. The value of OBAs should be weighed against the additional resources needed to administer such arrangements, and importantly overall cost to government.
© 2022. Crown.

Entities:  

Year:  2022        PMID: 36266557     DOI: 10.1007/s40273-022-01188-w

Source DB:  PubMed          Journal:  Pharmacoeconomics        ISSN: 1170-7690            Impact factor:   4.558


  27 in total

1.  Performance-based risk-sharing arrangements-good practices for design, implementation, and evaluation: report of the ISPOR good practices for performance-based risk-sharing arrangements task force.

Authors:  Louis P Garrison; Adrian Towse; Andrew Briggs; Gerard de Pouvourville; Jens Grueger; Penny E Mohr; J L Hans Severens; Paolo Siviero; Miguel Sleeper
Journal:  Value Health       Date:  2013-07-19       Impact factor: 5.725

Review 2.  Linking payment to health outcomes: a taxonomy and examination of performance-based reimbursement schemes between healthcare payers and manufacturers.

Authors:  Josh J Carlson; Sean D Sullivan; Louis P Garrison; Peter J Neumann; David L Veenstra
Journal:  Health Policy       Date:  2010-03-11       Impact factor: 2.980

3.  Are Payers Ready, Willing, and Able to Provide Access to New Durable Gene Therapies?

Authors:  Jane F Barlow; Mo Yang; J Russell Teagarden
Journal:  Value Health       Date:  2019-05-17       Impact factor: 5.725

4.  Recalibrating Health Technology Assessment Methods for Cell and Gene Therapies.

Authors:  Aris Angelis; Huseyin Naci; Allan Hackshaw
Journal:  Pharmacoeconomics       Date:  2020-12       Impact factor: 4.981

5.  FDA Approval of Tisagenlecleucel: Promise and Complexities of a $475 000 Cancer Drug.

Authors:  Peter B Bach; Sergio A Giralt; Leonard B Saltz
Journal:  JAMA       Date:  2017-11-21       Impact factor: 56.272

6.  Payer and Pharmaceutical Manufacturer Considerations for Outcomes-Based Agreements in the United States.

Authors:  Joshua D Brown; Rich Sheer; Margaret Pasquale; Lavanya Sudharshan; Kirsten Axelsen; Prasun Subedi; Daniel Wiederkehr; Fred Brownfield; Sachin Kamal-Bahl
Journal:  Value Health       Date:  2017-08-30       Impact factor: 5.725

7.  Managed Entry Agreements: Policy Analysis From the European Perspective.

Authors:  Monique Dabbous; Lylia Chachoua; Aleksandra Caban; Mondher Toumi
Journal:  Value Health       Date:  2020-04       Impact factor: 5.725

8.  A Systematic Review of Health Technology Assessments of Chimeric Antigen Receptor T-Cell Therapies in Young Compared With Older Patients.

Authors:  Amy Gye; Stephen Goodall; Richard De Abreu Lourenco
Journal:  Value Health       Date:  2021-08-28       Impact factor: 5.725

9.  Data collection infrastructure for patient outcomes in the UK - opportunities and challenges for cell and gene therapies launching.

Authors:  Jesper Jørgensen; Laura Mungapen; Panos Kefalas
Journal:  J Mark Access Health Policy       Date:  2019-02-04
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