Cost-effectiveness analysis of the tislelizumab versus docetaxel for advanced or metastatic non-small-cell lung cancer in China

Front Public Health. 2024 Jul 18:12:1425734. doi: 10.3389/fpubh.2024.1425734. eCollection 2024.

Abstract

Background: Tislelizumab is the first PD-1 inhibitor in China to demonstrate superior efficacy in second-line or third-line treatment of patients with advanced or metastatic non-small-cell lung cancer (NSCLC). This study aimed to evaluate the cost-effectiveness of tislelizumab compared to docetaxel from a Chinese healthcare system perspective.

Methods: A dynamic Markov model was developed to evaluate the cost-effectiveness of tislelizumab in comparison to docetaxel in second or third-line treatment. The efficacy data utilized in the model were derived from the RATIONALE-303 clinical trial, while cost and utility values were obtained from the drug data service platform and published studies. The primary outcomes of the model encompassed quality-adjusted life years (QALYs), costs, and incremental cost-effectiveness ratios (ICERs). One-way sensitivity analysis and probabilistic sensitivity analysis were conducted to validate the robustness of the base case analysis results.

Results: The tislelizumab group demonstrated a cost increase of CNY 117,473 and a gain of 0.58 QALYs compared to the docetaxel group, resulting in an ICER value of CNY 202,927 per QALY gained.

Conclusion: The administration of tislelizumab in patients with advanced or metastatic NSCLC not only extends the progression-free survival (PFS) and overall survival (OS). Moreover, this treatment demonstrates a favorable cost-effectiveness profile across the Chinese population.

Keywords: Markov model; NSCLC; cost-effectiveness; docetaxel; tislelizumab.

Publication types

  • Comparative Study

MeSH terms

  • Antibodies, Monoclonal, Humanized* / economics
  • Antibodies, Monoclonal, Humanized* / therapeutic use
  • Antineoplastic Agents / economics
  • Antineoplastic Agents / therapeutic use
  • Carcinoma, Non-Small-Cell Lung* / drug therapy
  • China
  • Cost-Effectiveness Analysis*
  • Docetaxel* / economics
  • Docetaxel* / therapeutic use
  • Female
  • Humans
  • Lung Neoplasms* / drug therapy
  • Male
  • Markov Chains
  • Middle Aged
  • Quality-Adjusted Life Years*

Substances

  • Antibodies, Monoclonal, Humanized
  • Antineoplastic Agents
  • Docetaxel
  • tislelizumab

Grants and funding

The author(s) declare that financial support was received for the research, authorship, and/or publication of this article. Funding for the production of this manuscript was provided by Shaanxi health research Fund project (project ID: 2022 D048), china. No funding or sponsorship was received for the publication of this article.