A novel CT-based radiomics model for predicting response and prognosis of chemoradiotherapy in esophageal squamous cell carcinoma (vol 14, 2039, 2024)

被引:3
|
作者
Kasai, Akinari [1 ]
Miyoshi, Jinsei [1 ,2 ]
Sato, Yasushi [1 ]
Okamoto, Koichi [1 ]
Miyamoto, Hiroshi [1 ]
Kawanaka, Takashi [3 ]
Tonoiso, Chisato [3 ]
Harada, Masafumi [3 ]
Goto, Masakazu [4 ]
Yoshida, Takahiro [4 ,5 ]
Haga, Akihiro [6 ]
Takayama, Tetsuji [1 ]
机构
[1] Tokushima Univ, Dept Gastroenterol & Oncol, Grad Sch Biomed Sci, 3-18-15 Kuramoto Cho, Tokushima 7708503, Japan
[2] Kawashima Hosp, Dept Gastroenterol, Tokushima, Japan
[3] Tokushima Univ, Dept Radiol, Grad Sch Biomed Sci, Tokushima, Japan
[4] Tokushima Univ, Dept Thorac Endocrine Surg & Oncol, Grad Sch Biomed Sci, Tokushima, Japan
[5] Yoshida Clin, Tokushima, Japan
[6] Tokushima Univ, Dept Med Image Informat, Grad Sch Biomed Sci, Tokushima, Japan
来源
SCIENTIFIC REPORTS | 2024年 / 14卷 / 01期
关键词
D O I
10.1038/s41598-024-52418-4
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
No clinically relevant biomarker has been identified for predicting the response of esophageal squamous cell carcinoma (ESCC) to chemoradiotherapy (CRT). Herein, we established a CT-based radiomics model with artificial intelligence (AI) to predict the response and prognosis of CRT in ESCC. A total of 44 ESCC patients (stage I-IV) were enrolled in this study; training (n = 27) and validation (n = 17) cohorts. First, we extracted a total of 476 radiomics features from three-dimensional CT images of cancer lesions in training cohort, selected 110 features associated with the CRT response by ROC analysis (AUC >= 0.7) and identified 12 independent features, excluding correlated features by Pearson's correlation analysis (r >= 0.7). Based on the 12 features, we constructed 5 prediction models of different machine learning algorithms (Random Forest (RF), Ridge Regression, Naive Bayes, Support Vector Machine, and Artificial Neural Network models). Among those, the RF model showed the highest AUC in the training cohort (0.99 [95%CI 0.86-1.00]) as well as in the validation cohort (0.92 [95%CI 0.71-0.99]) to predict the CRT response. Additionally, Kaplan-Meyer analysis of the validation cohort and all the patient data showed significantly longer progression-free and overall survival in the high-prediction score group compared with the low-prediction score group in the RF model. Univariate and multivariate analyses revealed that the radiomics prediction score and lymph node metastasis were independent prognostic biomarkers for CRT of ESCC. In conclusion, we have developed a CT-based radiomics model using AI, which may have the potential to predict the CRT response as well as the prognosis for ESCC patients with non-invasiveness and cost-effectiveness.
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