期刊
EUROPEAN RADIOLOGY
卷 31, 期 11, 页码 8438-8446出版社
SPRINGER
DOI: 10.1007/s00330-021-08004-7
关键词
Ovarian neoplasms; Peritoneal carcinomatosis; Magnetic resonance imaging; Radiomics
资金
- Applied Basic Research Programs of Shanxi Province [201801D221116]
A radiomics signature based on multisequence MRI is effective in predicting peritoneal metastasis in ovarian cancer patients. Combining clinical predictors, a nomogram can improve the prediction ability for peritoneal metastasis in patients with ovarian cancer.
Objectives To develop a radiomics signature based on multisequence magnetic resonance imaging (MRI) to preoperatively predict peritoneal metastasis (PM) in ovarian cancer (OC). Methods Eighty-nine patients with OC were divided into a training cohort including patients (n = 54) with a single lesion and a validation cohort including patients (n = 35) with bilateral lesions. Radiomics features were extracted from the T2-weighted images (T2WIs), fat-suppressed T2WIs, multi-b-value diffusion-weighted images (DWIs), and corresponding parametric maps. A radiomics signature and nomogram incorporating the radiomics signature and clinical predictors were developed and validated on the training and validation cohorts, respectively. Results The radiomics signature generated by 6 selected features showed a favorable discriminatory ability to predict PM in OC with an area under the curve (AUC) of 0.963 in the training cohort and an AUC of 0.928 in the validation cohort. The nomogram, comprising the radiomics signature, pelvic fluid, and CA-125 level, showed more favorable discrimination with an AUC of 0.969 in the training cohort and 0.944 in the validation cohort. Net reclassification index with values of 0.548 in the training cohort and 0.500 in the validation cohort. Conclusion Radiomics signature based on multisequence MRI serves as an effective quantitative approach to predict PM in OC patients. A nomogram of radiomics signature and clinical predictors could further improve the prediction ability of PM in patients with OC.
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