CT-based radiomics model to predict platinum sensitivity in epithelial ovarian carcinoma: a multicentre study

医学 无线电技术 曼惠特尼U检验 卵巢癌 内科学 曲线下面积 卵巢癌 化疗 肿瘤科 放射科 癌症
作者
Mengge He,Rahul Singh,Mandi Wang,Grace Ho,Esther Man Fung Wong,K.W. Chiu,Anthony K. T. Leung,Ka Yu Tse,Philip P.C. Ip,Andy Hwang,Lujun Han,Elaine Lee
出处
期刊:Cancer Imaging [BioMed Central]
卷期号:25 (1): 85-85 被引量:7
标识
DOI:10.1186/s40644-025-00906-9
摘要

OBJECTIVE: Platinum resistance carries poor prognosis in epithelial ovarian carcinoma (EOC). This study aimed to assess the value of radiomics model based on contrast-enhanced CT (ceCT) in predicting response to platinum-based chemotherapy in EOC. MATERIALS AND METHODS: Patients with histologically confirmed EOC and pre-treatment ceCT were retrospectively recruited from 5 centres. All patients underwent standard platinum-based chemotherapy and optimal cytoreduction. Platinum sensitivity was determined by whether it recurred within six months after platinum-based chemotherapy. The whole tumour volume was manually segmented on the baseline ceCT. Radiomics features were extracted using the open-source package PyRadiomics (version 3.0.1). Patients from centres A-C were randomly divided into training and internal validation sets in 4:1 ratio. Patients from the centres D and E were assigned as independent external validation sets. Spearman's rank correlation followed by 5-fold stratified cross validation (SCV) elastic net repeated for 100 times, and Mann-Whitney U test were deployed for feature reduction and selection. Adaptive synthetic sampling was applied to minimize class biases. Extra Trees classifier across 10-fold SCV was used for model building. The area under curve (AUC), calibration curve assessment, and decision curve analysis (DCA) were deployed to evaluate model performance and translational clinical utility. RESULTS: Seven hundred and three EOC patients (51.6 ± 9.3 years) were recruited. The training data (n = 608) yielded the following classification metrics: AUC (0.917), sensitivity (83.9%), specificity (94.4%), and accuracy (91.7%) in the internal validation set. The external validation set using centre D (n = 44) had AUC (0.877), sensitivity (76.5%), specificity (92.6%), and accuracy (86.4%); while centre E (n = 51) had AUC (0.845), sensitivity (73.3%), specificity (86.1%), and accuracy (82.4%) in predicting platinum sensitivity. DCA illustrated net clinical benefit in internal validation set and both external validation sets. CONCLUSIONS: The proposed CT-based radiomics model could be useful in predicting platinum sensitivity in EOC with potential in guiding personalized treatment in EOC.
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