Deep learning radiomics analysis based on computed tomography for survival prediction in gastric neuroendocrine neoplasm: a multicenter study

被引:4
作者
Yang, Zhihao [1 ,2 ]
Han, Yijing [1 ,2 ]
Li, Fei [3 ]
Zhang, Anqi [1 ,2 ]
Cheng, Ming [4 ]
Gao, Jianbo [1 ,2 ]
机构
[1] Zhengzhou Univ, Affiliated Hosp 1, Dept Radiol, Zhengzhou, Peoples R China
[2] Zhengzhou Univ, Affiliated Hosp 1, Henan Key Lab Image Diag & Treatment Digest Syst T, Zhengzhou, Peoples R China
[3] Wuhan Univ, Sch Cyber Sci & Engn, Wuhan, Peoples R China
[4] Zhengzhou Univ, Affiliated Hosp 1, Dept Med Informat, 1 Jianshe East Rd, Zhengzhou 450052, Peoples R China
关键词
Gastric neuroendocrine neoplasm (gNEN); survival analysis; computed tomography (CT); deep learning (DL); radiomics nomogram; CARCINOMA; CANCER; DIAGNOSTICS; PROGNOSIS; NOMOGRAM; HAZARDS; MODEL; G3;
D O I
10.21037/qims-23-577
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Background: Survival prediction is crucial for patients with gastric neuroendocrine neoplasms (gNENs) to assess the treatment programs and may guide personalized medicine. This study aimed to develop and evaluate a deep learning (DL) radiomics model to predict the overall survival (OS) in patients with gNENs.Methods: The retrospective analysis included 162 consecutive patients with gNENs from two hospitals, who were divided into a training cohort, internal validation cohort (The First Affiliated Hospital of Zhengzhou University; n=108), and an external validation cohort (The Henan Cancer Hospital; n=54). DL radiomics analysis was applied to computed tomography (CT) images of the arterial phase and venous phase, respectively. Based on pretreatment CT images, two DL radiomics signatures were developed to predict OS. The combined model incorporating the radiomics signatures and clinical factors was built through the multivariable Cox proportional hazards (CPH) method. The combined model was visualized into a radiomics nomogram for individualized OS estimation. Prediction performance was assessed with the concordance index (C-index) and the Kaplan-Meier (KM) estimator. Results: The DL-based radiomics signatures based on two phases were significantly correlated with OS in the training (C-index: 0.79-0.92; P<0.01), internal validation (C-index: 0.61-0.86; P<0.01), and external validation (C-index: 0.56-0.75; P<0.01) cohorts. The combined model integrating radiomics signatures with clinical factors showed a significant improvement in predictive performance compared to the clinical model in the training (C-index: 0.86 vs. 0.80; P<0.01), internal validation (C-index: 0.77 vs. 0.71; P<0.01), and external validation (C-index: 0.71 vs. 0.66; P<0.01) cohorts. Moreover, the combined model classified patients into high-risk and low-risk groups, and the high-risk group had a shorter OS compared to the low-risk group in the training cohort [hazard ratio (HR) 3.12, 95% confidence interval (CI): 2.34-3.93; P<0.01], which was validated in the internal (HR 2.51, 95% CI: 1.57-3.99; P<0.01) and external validation cohort (HR 1.77, 95% CI: 1.21-2.59; P<0.01).Conclusions: DL radiomics analysis could serve as a potential and noninvasive tool for prognostic prediction and risk stratification in patients with gNENs.
引用
收藏
页码:8190 / +
页数:17
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