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ORIGINAL RESEARCH article
Front. Pharmacol.
Sec. Drugs Outcomes Research and Policies
Volume 16 - 2025 | doi: 10.3389/fphar.2025.1563788
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Background: Advanced or metastatic squamous non-small cell lung cancer (NSCLC) represents a significant clinical and economic burden globally. In China, the introduction of innovative immunotherapy agents, such as penpulimab, has the potential to improve patient outcomes, but their high cost raises questions about affordability and cost-effectiveness. Objective: This study evaluates the economic viability of penpulimab combined with paclitaxel and carboplatin as a first-line treatment for this patient population. Methods: Data were obtained from the published randomized controlled trial AK105-302. A three-state partitioned survival model was developed to estimate the cost-effectiveness of the two treatments. One-way deterministic sensitivity analysis, probabilistic sensitivity analysis, and scenario analyses were performed to assess the robustness of the results and explore variations in key parameters. Results: The incremental cost-effectiveness ratio (ICER) for the penpulimab group compared to the placebo group was $16,105.90 per quality-adjusted life year (QALY), which falls below the willingness-to-pay (WTP) threshold of $37,709.46 per QALY. Deterministic sensitivity analysis identified the three most influential factors affecting model outcomes: discount rate, costs associated with progressive disease, and utility value for progression-free survival. Probabilistic sensitivity analysis indicated that at a WTP threshold of $37,709.46 per QALY, the probability of penpulimab being cost-effective reached 99%. Scenario analyses demonstrated that, while the base-case results were generally robust, the cost-effectiveness of penpulimab remained sensitive to the limited maturity of overall survival (OS) data in the penpulimab group. The immaturity of the OS data increased the extrapolation uncertainty, which could potentially alter the economic conclusions.Conclusion: Penpulimab, in combination with paclitaxel and carboplatin, demonstrates a cost-effectiveness advantage over placebo as a first-line treatment for advanced or metastatic squamous NSCLC in China, provided that long-term survival benefits align with extrapolations from the base case model. These findings support its prioritization in clinical practice within the current WTP thresholds. However, the economic conclusions remain contingent on resolving the uncertainties associated with immature OS data and validating extrapolation assumptions through extended follow-up studies.
Keywords: Non-small cell lung cancer, Penpulimab, partitioned survival model, Costeffectiveness analysis, Pharmacoeconomic evaluation
Received: 20 Jan 2025; Accepted: 27 Feb 2025.
Copyright: © 2025 You, Qin, Wang and Wang. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
* Correspondence:
Xianying Wang, Third Hospital of Hebei Medical University, Shijiazhuang, 050051, Hebei Province, China
Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.
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