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    Sotorasib Versus Docetaxel in Advanced Non-Small Cell Lung Cancer With Kras G12C Mutation: Cost-Effectiveness and Value of Information Analyses

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    Name:
    azu_etd_21783_sip1_m.pdf
    Embargo:
    2029-11-06
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    Author
    Aliu, Oiza Blessing
    Issue Date
    2024
    Keywords
    Cost-effectiveness analysis
    KRAS G12C mutation
    Non-small cell lung cancer
    Sotorasib
    Value of information analysis
    VOI
    Advisor
    Abraham, Ivo L.
    
    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 11/06/2029
    Abstract
    Background: Sotorasib is a first-in-class oral KRAS G12C inhibitor and has shown improved safety and efficacy compared to docetaxel in patients with advanced non-small cell lung cancer (NSCLC) who have KRAS G12C mutation and have previously been treated.Objective: To estimate the cost-effectiveness of sotorasib compared to docetaxel in KRAS G12C mutated advanced NSCLC and to determine the cost of uncertainty and whether future research will be beneficial by estimating the expected value of perfect information (EVPI). Methods: A 3-state partitioned survival model (progression-free, progressed, death) over a time horizon of 5 years and from a payer perspective in the United States was developed. Estimates of the progression-free and overall survival were determined from the Kaplan-Meier curves of the CodeBreak 200 trial based on the best-fitting parametric distribution. Costs of drugs and subsequent systemic treatments were sourced from Redbook, administration costs from Physician Fee Schedule, cost of adverse events management, and utilities from published literature. Model outcomes included incremental cost, quality-adjusted life-year (QALY), and incremental cost-utility ratio (ICUR). One-way and probabilistic sensitivity analyses (PSA) were used to account for the uncertainties in the model. Discounting at 3% per year was utilized. Using results from the PSA, the net health benefits (NHBs) and net monetary benefits (NMBs) forgone and population EVPI were calculated. Results: Sotorasib yielded an increase of 0.35 QALYs at an incremental cost of $329,619. At a willingness to pay threshold (WTP) of $150,000 per QALY, the incremental cost per QALY gained (ICUR) was $941,768. The acceptability curve indicated that the likelihood of attaining cost-effectiveness at $150,000 WTP was 3% vs. 97% for sotorasib and docetaxel respectively. The average per-patient NHBs and NMBs forgone were 0.061QALYs and $5019 respectively, while the population EVPI was estimated to be $627.3 million. Conclusion: Sotorasib may require a higher WTP threshold or a reduction in acquisition cost for it to be considered cost-effective. Additionally, uncertainty in its clinical efficacy compared to docetaxel persists, and future research to acquire additional evidence may be beneficial.
    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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