Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2025 Jun 25:16:1594786.
doi: 10.3389/fimmu.2025.1594786. eCollection 2025.

Cost-effectiveness analysis of cadonilimab plus bevacizumab and chemotherapy for persistent, recurrent, or metastatic cervical cancer

Affiliations

Cost-effectiveness analysis of cadonilimab plus bevacizumab and chemotherapy for persistent, recurrent, or metastatic cervical cancer

Kaixuan Wang et al. Front Immunol. .

Abstract

Objective: The aim of this study is to investigate the cost-effectiveness of cadonilimab plus bevacizumab and chemotherapy in the first-line treatment for patients with persistent, recurrent, or metastatic cervical cancer from a healthcare system perspective in China.

Methods: A partitioned survival model was established to estimate the total costs, quality-adjusted life-years (QALYs), and incremental cost-effectiveness ratio (ICER) over a 10-year time horizon. Clinical data was sourced from the COMPASSION-16 trial; direct medical costs and utilities were obtained from a public drug bidding database and published literature. The robustness of the model was assessed via scenario, one-way and probabilistic sensitivity analyses.

Results: Cadonilimab plus bevacizumab and chemotherapy yielded an additional cost of $31,654.02, with an additional QALY of 0.36, resulted in an ICER of $88,533.51/QALY compared with bevacizumab and chemotherapy. Utility values of progression-free survival (PFS), patient weight and price of cadonilimab were the most influential parameter on ICER. The probability of cadonilimab plus bevacizumab and chemotherapy being cost-effective was 0% at the WTP threshold of $38,042.49 per QALY. When the price of cadonilimab reduced by 72%, cadonilimab plus bevacizumab and chemotherapy would represent an economically viable treatment regime.

Conclusion: Cadonilimab plus bevacizumab and chemotherapy may not be a cost-effective option as the first-line treatment in persistent, recurrent, or metastatic cervical cancer.

Keywords: bevacizumab; cadonilimab; cervical cancer; chemotherapy; cost-effectiveness.

PubMed Disclaimer

Conflict of interest statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Figures

Figure 1
Figure 1
The structure of the partitioned survival model.
Figure 2
Figure 2
Scenario analysis results for price reductions of cadonilimab. ICER, incremental cost-effectiveness ratio; WTP, willingness to Pay.
Figure 3
Figure 3
Tornado diagram of one-way sensitivity analysis results. ICER, incremental cost-effectiveness ratio; QALY, quality-adjusted life year; CBC, cadonilimab plus bevacizumab and chemotherapy; BC, bevacizumab and chemotherapy; PFS, progression-free survival; PD, progressive disease.
Figure 4
Figure 4
The incremental cost-effectiveness scatter plot of cadonilimab plus bevacizumab and chemotherapy compared to bevacizumab and chemotherapy in China. QALY, quality-adjusted life year; WTP, willingness to Pay.
Figure 5
Figure 5
The cost-effectiveness acceptability curve of the probabilistic sensitivity analysis results. CBC, cadonilimab plus bevacizumab and chemotherapy; BC, bevacizumab and chemotherapy; QALY, quality-adjusted life year; WTP, willingness to Pay.

Similar articles

References

    1. Bray F, Laversanne M, Sung H, Ferlay J, Siegel RL, Soerjomataram I, et al. Global cancer statistics 2022: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin. (2024) 74:229–63. doi: 10.3322/caac.21834 - DOI - PubMed
    1. Han B, Zheng R, Zeng H, Wang S, Sun K, Chen R, et al. Cancer incidence and mortality in China, 2022. J Natl Cancer Cent. (2024) 4:47–53. doi: 10.1016/j.jncc.2024.01.006 - DOI - PMC - PubMed
    1. Li S, Hu T, Lv W, Zhou H, Li X, Yang R, et al. Changes in prevalence and clinical characteristics of cervical cancer in the People’s Republic of China: a study of 10,012 cases from a nationwide working group. Oncologist. (2013) 18:1101–7. doi: 10.1634/theoncologist.2013-0123 - DOI - PMC - PubMed
    1. Gennigens C, Jerusalem G, Lapaille L, De Cuypere M, Streel S, Kridelka F, et al. Recurrent or primary metastatic cervical cancer: current and future treatments. ESMO Open. (2022) 7:100579. doi: 10.1016/j.esmoop.2022.100579 - DOI - PMC - PubMed
    1. Tewari KS, Sill MW, Penson RT, Huang H, Ramondetta LM, Landrum LM, et al. Bevacizumab for advanced cervical cancer: final overall survival and adverse event analysis of a randomised, controlled, open-label, phase 3 trial (Gynecologic Oncology Group 240). Lancet. (2017) 390:1654–63. doi: 10.1016/S0140-6736(17)31607-0 - DOI - PMC - PubMed

MeSH terms

Substances