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Cost-effectiveness of biomarker-based and universal strategies for the treatment of advanced-stage endometrial cancer.

Publication ,  Journal Article
Bashi, A; Chen, L; Rouse, K; Elkin, EB; Ferris, JS; Xu, X; Bickell, NA; Blank, S; Rossi, EC; Hazelton, WD; Wright, JD; Havrilesky, LJ; Myers, ER
Published in: Gynecol Oncol
December 2025

OBJECTIVE: To compare cost-effectiveness of targeted therapeutic strategies for non-Hispanic Black (NHB) and non-Hispanic White (NHB) patients with newly diagnosed, advanced-stage endometrial cancer. METHODS: A Markov-based cost-utility model using a third-party payer perspective compared concurrent and maintenance treatment strategies incorporating dostarlimab and trastuzumab for newly diagnosed stage III-IV endometrial cancer: chemotherapy alone; 3 universal immunotherapy strategies (universal concurrent and maintenance dostarlimab +/- trastuzumab for HER2/neu-positive serous and/or carcinosarcomas); and 3 targeted immunotherapy strategies (dostarlimab for mismatch repair deficient (dMMR) tumors +/- trastuzumab for HER2/neu positive serous and/or carcinosarcomas). Costs (2024 USD), utilities, and clinical estimates were derived from published literature and the National Cancer Database. The base case analysis was a microsimulation with 10,000 runs, accompanied by a Monte Carlo probabilistic sensitivity analysis with 20,000 trials. Cost-effectiveness was assessed using incremental cost-effectiveness ratios (ICERs) with a willingness-to-pay threshold of $150,000/quality-adjusted life year (QALY). We performed one-way and two-way sensitivity analyses on key parameters and analyses stratified by race/ethnicity. RESULTS: All targeted immunotherapy strategies were cost-effective compared to chemotherapy alone in both NHB and NHW, while universal immunotherapy was never cost-effective. Targeted strategies were more cost-effective in NHB than NHW. Targeted dostarlimab for dMMR plus trastuzumab for HER2 serous and carcinosarcomas was the most cost-effective strategy compared to chemotherapy, with an ICER of $119,945/QALY. In sensitivity analysis, assuming longer durations of treatment benefit resulted in lower ICERs. CONCLUSIONS: Personalized treatment strategies incorporating HER2 and MMR testing should be considered to optimize both cost-effectiveness and equity in care.

Duke Scholars

Published In

Gynecol Oncol

DOI

EISSN

1095-6859

Publication Date

December 2025

Volume

203

Start / End Page

130 / 138

Location

United States

Related Subject Headings

  • White
  • Trastuzumab
  • Receptor, erbB-2
  • Receptor, ErbB-2
  • Quality-Adjusted Life Years
  • Oncology & Carcinogenesis
  • Neoplasm Staging
  • Markov Chains
  • Immunotherapy
  • Humans
 

Citation

APA
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MLA
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Bashi, A., Chen, L., Rouse, K., Elkin, E. B., Ferris, J. S., Xu, X., … Myers, E. R. (2025). Cost-effectiveness of biomarker-based and universal strategies for the treatment of advanced-stage endometrial cancer. Gynecol Oncol, 203, 130–138. https://doi.org/10.1016/j.ygyno.2025.09.019
Bashi, Aya, Ling Chen, Kevin Rouse, Elena B. Elkin, Jennifer S. Ferris, Xiao Xu, Nina A. Bickell, et al. “Cost-effectiveness of biomarker-based and universal strategies for the treatment of advanced-stage endometrial cancer.Gynecol Oncol 203 (December 2025): 130–38. https://doi.org/10.1016/j.ygyno.2025.09.019.
Bashi A, Chen L, Rouse K, Elkin EB, Ferris JS, Xu X, et al. Cost-effectiveness of biomarker-based and universal strategies for the treatment of advanced-stage endometrial cancer. Gynecol Oncol. 2025 Dec;203:130–8.
Bashi, Aya, et al. “Cost-effectiveness of biomarker-based and universal strategies for the treatment of advanced-stage endometrial cancer.Gynecol Oncol, vol. 203, Dec. 2025, pp. 130–38. Pubmed, doi:10.1016/j.ygyno.2025.09.019.
Bashi A, Chen L, Rouse K, Elkin EB, Ferris JS, Xu X, Bickell NA, Blank S, Rossi EC, Hazelton WD, Wright JD, Havrilesky LJ, Myers ER. Cost-effectiveness of biomarker-based and universal strategies for the treatment of advanced-stage endometrial cancer. Gynecol Oncol. 2025 Dec;203:130–138.
Journal cover image

Published In

Gynecol Oncol

DOI

EISSN

1095-6859

Publication Date

December 2025

Volume

203

Start / End Page

130 / 138

Location

United States

Related Subject Headings

  • White
  • Trastuzumab
  • Receptor, erbB-2
  • Receptor, ErbB-2
  • Quality-Adjusted Life Years
  • Oncology & Carcinogenesis
  • Neoplasm Staging
  • Markov Chains
  • Immunotherapy
  • Humans