Modification of gemcitabine with oxaliplatin in China for unresectable gallbladder cancer: a cost-effectiveness analysis

Front Public Health. 2024 Dec 13:12:1432947. doi: 10.3389/fpubh.2024.1432947. eCollection 2024.

Abstract

Background: The incidence of gall bladder cancer (GBC), one of the most prevalent bile duct malignancies, differs with ethnicity and geographic location. To treat unresected GBC in the Chinese setting, this study aimed to assess the financial effectiveness of a combination of modified gemcitabine and oxaliplatin.

Methods: Data from a randomized controlled study in which individuals with metastatic GBC were treated with oxaliplatin and gemcitabine demonstrated improved survival. A Markov model is built to calculate the incremental cost-benefit ratio (ICER) from the viewpoint of Chinese society on the basis of clinical symptoms and disease development. One-way certainty and probability sensitivity analyses are used to describe the uncertainty in the model.

Results: Compared with those of fluorouracil (FU) and folinic acid, the utility value of modified oxaliplatin combined with gemcitabine increased by 0.22QALY throughout the course of the 10-year simulation (FA). In a Chinese healthcare setting, the cost-effectiveness ratio (ICER) is $52765.59/QALY, with a 0% chance of cost-benefit at the WTP (willing-to-pay) level of $37697.00/QALY. The ICERs predicted by sensitivity analysis were not significantly affected by cost variations related to the management of Grade 3-4 AEs, the diagnostics used, or hospitalization expenditures.

Conclusion: In a Chinese healthcare context, modified gemcitabine coupled with oxaliplatin (mGEMOX) is not a cost-effective treatment option for unresectable GBC.

Keywords: cost effectiveness; fluorouracil; gallbladder cancer (GBC); gemcitabine; oxaliplatin.

MeSH terms

  • Antineoplastic Combined Chemotherapy Protocols* / economics
  • Antineoplastic Combined Chemotherapy Protocols* / therapeutic use
  • China
  • Cost-Benefit Analysis*
  • Cost-Effectiveness Analysis
  • Deoxycytidine* / analogs & derivatives
  • Deoxycytidine* / economics
  • Deoxycytidine* / therapeutic use
  • Female
  • Gallbladder Neoplasms* / drug therapy
  • Gemcitabine*
  • Humans
  • Male
  • Markov Chains*
  • Middle Aged
  • Oxaliplatin* / economics
  • Oxaliplatin* / therapeutic use
  • Quality-Adjusted Life Years

Substances

  • Deoxycytidine
  • Gemcitabine
  • Oxaliplatin

Grants and funding

The author(s) declare that financial support was received for the research, authorship, and/or publication of this article. This work was supported by the National Clinical Research Center for Geriatrics, West China Hospital, Sichuan University (Z2024YY003) and the 1 • 3 • 5 project for disciplines of excellence-Clinical Research Fund, West China Hospital, Sichuan University (2024HXFH015).