The interpretable CT-based vision transformer model for preoperative prediction of clear cell renal cell carcinoma SSIGN score and outcome.

IF 4.1 2区 医学 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING
Kaiyue Zhi, Yanmei Wang, Lei Yan, Feng Hou, Jie Wu, Shuo Zhang, He Zhu, Lianzi Zhao, Ning Wang, Xia Zhao, Xianjun Li, Yicong Wang, Chengcheng Chen, Nan Wang, Yuchao Xu, Guangjie Yang, Pei Nie
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引用次数: 0

Abstract

Objectives: To develop and validate an interpretable CT-based vision transformer (ViT) model for preoperative prediction of the stage, size, grade, and necrosis (SSIGN) and outcome in clear cell renal cell carcinoma (ccRCC) patients.

Methods: Eight hundred forty-five ccRCC patients from multiple centers were retrospectively enrolled. For each patient, 768 ViT features were extracted in the cortical medullary phase (CMP) and renal parenchymal phase (RPP) images, respectively. The CMP ViT model (CVM), RPP ViT model (RVM), and CMP-RPP combined ViT model (CRVM) were constructed to predict the SSIGN in ccRCC patients. The area under the receiver operating characteristic curve (AUC) was used to evaluate the performance of each model. Decision curve analysis (DCA) was used to evaluate the net clinical benefit. The endpoint was the progression-free survival (PFS). Kaplan-Meier survival analysis was used to assess the association between model-predicted SSIGN and PFS. The SHAP approach was applied to determine the prediction process of the CRVM.

Results: The CVM, RVM, and CRVM demonstrated good performance in predicting SSIGN, with a high AUC of 0.859, 0.883, and 0.895, respectively, in the test cohort. DCA demonstrated the CRVM performed best in clinical net benefit. In predicting PFS, CRVM achieved a higher Harrell's concordance index (C-index, 0.840) than the CVM (0.719) and RVM (0.773) in the test cohort. The SHAP helped us understand the impact of ViT features on CRVM's SSIGN prediction from a global and individual perspective.

Conclusion: The interpretable CT-based CRVM may serve as a non-invasive biomarker in predicting the SSIGN and outcome of ccRCC.

Critical relevance statement: Our findings outline the potential of an interpretable CT-based ViT biomarker for predicting the SSIGN score and outcome of ccRCC, which might facilitate patient counseling and assist clinicians in therapy decision-making for individual cases.

Key points: Current first-line imaging lacks preoperative prediction of the SSIGN score for ccRCC patients. The ViT model could predict the SSIGN score and outcome of ccRCC patients. This study can facilitate the development of personalized treatment for ccRCC patients.

透明细胞肾细胞癌术前预测SSIGN评分及预后的可解释ct视觉转换模型。
目的:开发并验证一种可解释的基于ct的视觉变形(ViT)模型,用于透明细胞肾细胞癌(ccRCC)患者的分期、大小、分级、坏死(SSIGN)和预后的术前预测。方法:回顾性纳入来自多个中心的845例ccRCC患者。每位患者分别在皮质髓质期(CMP)和肾实质期(RPP)图像中提取768个ViT特征。构建CMP ViT模型(CVM)、RPP ViT模型(RVM)、CMP-RPP联合ViT模型(CRVM)预测ccRCC患者的SSIGN。采用受试者工作特征曲线下面积(AUC)评价各模型的性能。采用决策曲线分析(DCA)评价净临床获益。终点是无进展生存期(PFS)。Kaplan-Meier生存分析用于评估模型预测的SSIGN与PFS之间的关系。采用SHAP方法确定CRVM的预测过程。结果:CVM、RVM和CRVM在预测SSIGN方面表现良好,在测试队列中AUC分别为0.859、0.883和0.895。DCA证明CRVM在临床净收益方面表现最佳。在预测PFS方面,CRVM的Harrell’s一致性指数(C-index, 0.840)高于CVM(0.719)和RVM(0.773)。SHAP帮助我们从全局和个体的角度理解ViT特征对CRVM的SSIGN预测的影响。结论:基于ct的可解释性CRVM可作为预测ccRCC SSIGN及预后的无创生物标志物。关键相关性声明:我们的研究结果概述了一种可解释的基于ct的ViT生物标志物的潜力,用于预测ccRCC的SSIGN评分和结果,这可能有助于患者咨询,并协助临床医生针对个别病例做出治疗决策。重点:目前一线影像学缺乏对ccRCC患者SSIGN评分的术前预测。ViT模型可以预测ccRCC患者的SSIGN评分及预后。本研究可以促进ccRCC患者个性化治疗的发展。
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来源期刊
Insights into Imaging
Insights into Imaging Medicine-Radiology, Nuclear Medicine and Imaging
CiteScore
7.30
自引率
4.30%
发文量
182
审稿时长
13 weeks
期刊介绍: Insights into Imaging (I³) is a peer-reviewed open access journal published under the brand SpringerOpen. All content published in the journal is freely available online to anyone, anywhere! I³ continuously updates scientific knowledge and progress in best-practice standards in radiology through the publication of original articles and state-of-the-art reviews and opinions, along with recommendations and statements from the leading radiological societies in Europe. Founded by the European Society of Radiology (ESR), I³ creates a platform for educational material, guidelines and recommendations, and a forum for topics of controversy. A balanced combination of review articles, original papers, short communications from European radiological congresses and information on society matters makes I³ an indispensable source for current information in this field. I³ is owned by the ESR, however authors retain copyright to their article according to the Creative Commons Attribution License (see Copyright and License Agreement). All articles can be read, redistributed and reused for free, as long as the author of the original work is cited properly. The open access fees (article-processing charges) for this journal are kindly sponsored by ESR for all Members. The journal went open access in 2012, which means that all articles published since then are freely available online.
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