Why the study?
To develop and validate a combined model based on ultrasound radiomics to detect cardiotoxicity after chemotherapy in patients with breast cancer.
Does a combined model based on ultrasound radiomics improve the detection of post-chemotherapy cardiotoxicity in breast cancer patients compared to clinical or radiomics models alone?
Does a combined model based on ultrasound radiomics improve the detection of post-chemotherapy cardiotoxicity in breast cancer patients compared to clinical or radiomics models alone?
A combined ultrasound radiomics and clinical model demonstrates high diagnostic accuracy for the early detection of chemotherapy-induced cardiotoxicity in breast cancer patients.
Answers are grounded in this paper and cite their sources.
Radiomics model may aid cardiotoxicity detection after breast cancer chemotherapy; leaves open prospective validation before clinical use.
Purpose The aim of this study is to develop and validate a combined model based on ultrasound radiomics to detect cardiotoxicity after chemotherapy in patients with breast cancer. Methods In this paper, we included 208 patients with breast cancer diagnosed pathologically and after chemotherapy, of whom had high‐quality echocardiographic images; among them, 105 cases experienced cardiotoxicity, while 103 cases did not, which were divided into a training set and a validation set using a wholly randomized method according to a ratio of 7:3. Then, the left ventricular myocardium in the parasternal long‐axis view of echocardiography was manually traced, the myocardial features of each image were extracted and filtered, and then a radiomics model was established; lastly, we plotted the receiver operating characteristic (ROC) curve; calculated the area under the curve (AUC); and assessed the diagnostic performance of the model. Results The AUC of the combined model in the training set was 0.88 (95%CI,0.828–0.936), which was higher than the clinical model at 0.73 (95%CI,0.646–0.807) and the radiomics model at 0.84 (95%CI,0.774–0.903). In the validation set, the AUC of the combined model was 0.87 (95%CI,0.783–0.959), which was higher than the clinical model at 0.75 (95%CI,0.631–0.877) and the radiomics model at 0.81 (95%CI,0.698–0.917). The combined model of the training group and the validation group had statistical significance compared to both the clinical model and the radiomics model ( Z = −4.066, p < 0.001; Z = −1.977, p = 0.048); ( Z = −1.986, p = 0.047; Z = −2.142, p = 0.032). Meanwhile, the results of Hosmer–Lemeshow goodness‐of‐fit test were favorable (the training group: X 2 = 6.776, p = 0.561; the validation group: X 2 = 11.949, p = 0.154). Conclusion The combined model based on radiomics is an effective tool for the early diagnosis of cardiac toxicity in breast cancer patients after chemotherapy. It helps to detect cardiotoxicity of breast cancer patients during chemotherapy.
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Xia et al. (2025) studied this question.
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