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    Economic Evaluation For The United States (US) of Overall Survival Benefits Of Tebentafusp in Metastatic Uveal Melanoma

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    azu_etd_20326_sip1_m.pdf
    Embargo:
    2026-04-11
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    Author
    Aqel, Osama
    Issue Date
    2023
    Keywords
    Cost-effectivness
    Economic-evalulation
    Immunotherapy
    Metastatic uveal melanoma
    Tebentafusp
    Advisor
    Abraham, Ivo
    
    Metadata
    Show full item record
    Publisher
    The University of Arizona.
    Rights
    Copyright © is held by the author. Digital access to this material is made possible by the University Libraries, University of Arizona. Further transmission, reproduction, presentation (such as public display or performance) of protected items is prohibited except with permission of the author.
    Embargo
    Release after 04/11/2026
    Abstract
    Tebentafusp was recently approved for the treatment of metastatic uveal melanoma patients. This study aimed to perform an industry-independent pharmacoeconomic evaluation of this regimen versus investigator choice of treatment (ICOT).Two (without and with vial wastage) three-state (progression-free, progressed, death) partitioned survival models were developed to compare costs and overall survival (OS) outcomes associated with both treatments from the US payer perspective. Progression-free survival (PFS) and OS curves were digitized, and parametric functions fitted against a 5-year time horizon. Medication costs (Wholesale Acquisition Costs) were sourced from Red Book; administration and monitoring parameters from US government databases; and costs of adverse event management (grade 3/4 with rate ≥5%) from prior uveal melanoma and advanced melanoma economic evaluations. Life years (LY), quality-adjusted life years (QALY), and incremental cost-effectiveness/utility ratios (ICER/ICUR) were estimated in the base case (BCA) and probabilistic sensitivity analyses (PSA). Cost-effectiveness planes and acceptability curves were plotted against different willingness-to-pay (WTP) thresholds. Excluding vial wastage, BCA (PSA) showed an incremental cost of tebentafusp over ICOT of $378,103 ($378,105), incremental LY of 0.72 (0.72), and incremental QALY of 0.46 (0.46); yielding ICER of $525,143 ($525,146) per LY gained (g) and ICUR of an incremental cost of $821,963 ($821,967) per QALYg. Tebentafusp has 50% and 100% probabilities of being cost-effective at WTP thresholds of $820,000 and $1,200,000 or above, respectively. The corresponding estimates, including vial wastage, are incremental costs of $577,759 ($578,499), yielding ICER of an incremental cost of $802,443 ($792,464) per LYg, ICUR of an incremental cost of $1,255,998 ($1,257,607) per QALYg, with 50% and 100% probabilities at WTPs of $1,255,500 and $1,750,000. This independent economic evaluation demonstrates that tebentafusp is associated with improved 5-year OS outcome over ICOT, yet at a higher cost. Vial wastage is a major and avoidable cost driver.
    Type
    text
    Electronic Thesis
    Degree Name
    M.S.
    Degree Level
    masters
    Degree Program
    Graduate College
    Pharmaceutical Sciences
    Degree Grantor
    University of Arizona
    Collections
    Master's Theses

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