Ultrasound-based radiomics for predicting the five major histological subtypes of epithelial ovarian cancer

Background Computational approaches have been proposed using radiomics in order to assess tumour heterogeneity, which is motivated by the concept that biomedical images may contain underlying pathophysiology information and has the potential to quantitatively measure the heterogeneity of intra- and...

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Published inBMC medical imaging Vol. 25; no. 1; pp. 122 - 13
Main Authors Yang, Yang, Ji, Xinyu, Li, Sen, Gao, Xuemeng, Wang, Yitong, Huang, Ying
Format Journal Article
LanguageEnglish
Published London BioMed Central 15.04.2025
BioMed Central Ltd
BMC
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ISSN1471-2342
1471-2342
DOI10.1186/s12880-025-01624-1

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Summary:Background Computational approaches have been proposed using radiomics in order to assess tumour heterogeneity, which is motivated by the concept that biomedical images may contain underlying pathophysiology information and has the potential to quantitatively measure the heterogeneity of intra- and intertumours. Ovarian cancer has the highest mortality among malignant tumours of female reproductive system and can be further divided into many subtypes with different management strategies and prognosis. The purpose of our study is to develop and validate ultrasound-based radiomics models to distinguish the five major histological subtypes of epithelial ovarian cancer. Methods From January 2018 to August 2022, 1209 eligible ovarian cancer patients were enrolled. There were two subjects in this study: all patients ( n  = 1209) and patients with the five major histological subtypes ( n  = 1039). After image segmentation manually, radiomics features were extracted and some clinical characteristics were added. Nine feature selection methods were used to select the optimal predictive features. Seven classifiers were carried out to construct models. Choose the combination with the best predictive performance as the final result. Results As for low-grade serous carcinoma, endometrioid carcinoma, and clear cell carcinoma, the models yields AUCs below 0.80 in the 10-fold cross-validation in the two groups. As for mucinous carcinoma, the AUCs were 0.83(95% CI , 0.74–0.93) and 0.89(95% CI , 0.83–0.95) in the validation cohorts and 0.80(95% CI , 0.73–0.87) and 0.86(95% CI , 0.78–0.94) in the 10-fold cross-validation in the two groups, respectively. As for high-grade serous carcinoma (HGSC), the models showed AUCs of 0.87(95% CI , 0.83–0.91) and 0.85(95% CI , 0.81–0.89) in the validation cohorts and 0.87(95% CI , 0.85–0.89) and 0.84(95% CI , 0.81–0.87) in the 10-fold cross-validation in the two groups, respectively, and exhibited high consistency between the predicted results and the actual outcomes, and brought great net benefits for patients. Conclusions The ultrasound-based radiomics models in discriminating HGSC and non-HGSC showed good predictive performance, as well as high consistency between the predicted results and the actual outcomes, and brought significant net benefits for patients.
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ISSN:1471-2342
1471-2342
DOI:10.1186/s12880-025-01624-1