Evidence map›Paper›PMID 41543782›Full record

ArticleDiscover oncology2026

A clinically translatable pathomics-based predictive model for preoperative prognostic assessment in patients with endometrial cancer.

Jing Liu, Hongyan Zhao, Xuesong Zhang, Lili Liu, Liqian Zhang

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Article in Discover oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

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5 authors.

Jing LiuDepartment of Gynecology, Tangshan Maternity and Child Healthcare Hospital, Tangshan, 063000, Hebei Province, China.
Hongyan ZhaoDepartment of Gynecology, Tangshan Maternity and Child Healthcare Hospital, Tangshan, 063000, Hebei Province, China.
Xuesong ZhangDepartment of Gynecology, Tangshan Maternity and Child Healthcare Hospital, Tangshan, 063000, Hebei Province, China.
Lili LiuDepartment of Hospital Infection Management, Tangshan Maternity and Child Healthcare Hospital, Tangshan, 063000, Hebei Province, China.
Liqian ZhangDepartment of Gynecology, Tangshan Maternity and Child Healthcare Hospital, Tangshan, 063000, Hebei Province, China. 352699188@qq.com.

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6 · The paper itself

Abstract

backgroundEndometrial cancer (EC) is a common gynecologic malignancy with rising incidence and significant molecular heterogeneity. This study aimed to develop an integrated prognostic model using pathomics features derived from histopathological images.

methodsWe retrospectively analyzed hematoxylin and eosin-stained whole slide images and clinical data from 511 EC patients in the TCGA database. Pathomics features were extracted using the same methodology as the reference study. Patients were randomly divided into training (n = 341) and validation (n = 170) cohorts at a 2:1 ratio. Under a leave-one-out cross-validation framework, features were selected using LASSO combined with random survival forest to construct a pathomics score. Differential gene expression and functional enrichment were analyzed and a nomogram integrating the pathomics score with clinical variables was developed and evaluated.

resultsThe pathomics model demonstrated excellent prognostic prediction, with AUCs of 0.966, 0.724, and 0.918 in the training, validation, and whole cohorts for 5-year survival, respectively. The pathomics score showed significant associations with FIGO stage, grade, lymph node metastasis, and recurrence (p < 0.05). Differential gene expression analysis revealed enrichment in EC-related pathways, MAPK signaling, estrogen signaling, and HIF-1 signaling pathways. Multivariable analysis confirmed FIGO stage, grade, lymph node metastasis, and pathomics score as independent prognostic factors. The nomogram incorporating these factors showed significantly improved in overall survival (all p < 0.001 in the 3 cohorts) and predictive evaluation of AUCs (increases of 0.111, 0.132, and 0.118, respectively) with good calibration.

conclusionThe proposed nomogram integrating pathomics and clinical factors provides accurate prognostic prediction for EC patients, offering a valuable tool for risk stratification and personalized management.

Indexed as

Endometrial cancerLOOCVMachine learningPathomicsPrognosis

Identifiers

PMID41543782
PMCPMC12891266

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