一项大规模诊断研究表明,具有巩固与肿瘤比(CTR)先验的贝叶斯深度学习模型彻底改变了IA期肺腺癌通过空气间隙扩散(STAS)的预测。

IF 3.5 2区 医学 Q2 ONCOLOGY
Translational lung cancer research Pub Date : 2025-05-30 Epub Date: 2025-05-27 DOI:10.21037/tlcr-24-890
Jie Cao, Nan Chen, Lingyu Zhou, Le Yi, Zhiyu Peng, Lin Qiu, Haokun Wu, Xiyue Tan, Kunhao Wu, Huahang Lin, Zhaokang Huang, Zetao Liu, Chenglin Guo, Xiuyuan Xu, Zhang Yi, Jiandong Mei
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引用次数: 0

摘要

背景:早期肺腺癌(LUAD)患者术前预测肺间隙扩散(STAS)对于选择合适的手术入路和改善患者预后至关重要。既往研究证实,实变与肿瘤比(CTR)与STAS之间存在显著相关性。本研究旨在建立基于CTR的贝叶斯深度学习(DL)模型,以预测IA期LUAD患者的STAS。方法:这项大规模诊断研究纳入了2017年11月至2023年10月期间接受完全切除的孤立性原发性侵袭性LUAD患者。入组患者按7:2:1的比例随机分配到训练组、验证组和试验组。利用变分贝叶斯推理框架,我们开发了一个基于CTR先验的深度学习模型(STAS-DLPrior CTR)。采用受试者工作特征(ROC)曲线、校准曲线、决策曲线分析(DCA)和临床影响曲线(CIC),将tas - dlprior CTR与另一种无CTR先验的DL模型(tas - dlnon -prior CTR)的性能进行比较。结果:共纳入1374例患者,其中训练组961例,验证组275例,试验组138例。结果显示,stas阳性组的CTR显著高于stas阴性组[0.63(四分位数间距,0.36,0.98)比0.35(四分位数间距,0.19,0.60)],p非先验CTR,验证队列中STAS-DLPrior CTR的ROC曲线下面积(AUC)趋于较高(0.831比0.731,P=0.06),检验队列中STAS-DLPrior CTR的AUC显著高于阴性组(0.858比0.637,P=0.008)。此外,校准曲线表明对STAS-DLPrior CTR的校准效果更好。DCA和CIC也表明,STAS-DLPrior CTR具有更高的临床净获益。结论:基于CTR先验的模型在预测IA期LUAD患者STAS方面具有显著优势,将医生知识作为先验可以有效指导DL模型的开发。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Bayesian deep learning model with consolidation-to-tumor ratio (CTR) prior revolutionizes the prediction of spread through air spaces (STAS) in stage IA lung adenocarcinoma: a large-scale diagnostic study.

Background: The preoperative prediction of spread through air spaces (STAS) in patients with early-stage lung adenocarcinoma (LUAD) is crucial for selecting the appropriate surgical approach and improving patient outcomes. Previous research has confirmed that there is a significant correlation between consolidation-to-tumor ratio (CTR) and STAS. This study aimed to develop a Bayesian deep learning (DL) model based on the CTR prior to predict STAS in patients with stage IA LUAD.

Methods: This large-scale diagnostic study included patients with solitary primary invasive LUAD who underwent complete resection between November 2017 and October 2023. Enrolled patients were randomly assigned to training, validation, and test cohorts in a 7:2:1 ratio. Using a variational Bayesian inference framework, we developed a DL model based on the CTR prior (STAS-DLPrior CTR). The performance of STAS-DLPrior CTR was compared with another DL model without the CTR prior (STAS-DLNon-prior CTR) using the receiver operating characteristic (ROC) curve, calibration curve, decision curve analysis (DCA), and clinical impact curve (CIC).

Results: A total of 1,374 patients were included, with 961 in the training cohort, 275 in the validation cohort, and 138 in the test cohort. The results showed that CTR in the STAS-positive group was significantly higher than that in the STAS-negative group [0.63 (interquartile range, 0.36, 0.98) vs. 0.35 (interquartile range, 0.19, 0.60), P<0.001]. Compared to STAS-DLNon-prior CTR, the area under the ROC curve (AUC) tends to be higher for STAS-DLPrior CTR (0.831 vs. 0.731, P=0.06) in the validation cohort, and STAS-DLPrior CTR demonstrated a significantly higher AUC (0.858 vs. 0.637, P=0.008) in the test cohort. Additionally, the calibration curve suggested better calibration for STAS-DLPrior CTR. DCA and CIC also indicated that STAS-DLPrior CTR conferred higher clinical net benefit.

Conclusions: The proposed model based on the CTR prior offers significant advantages in predicting STAS in patients with stage IA LUAD, and incorporating doctors' knowledge as priors can effectively guide the development of DL models.

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来源期刊
CiteScore
7.20
自引率
2.50%
发文量
137
期刊介绍: Translational Lung Cancer Research(TLCR, Transl Lung Cancer Res, Print ISSN 2218-6751; Online ISSN 2226-4477) is an international, peer-reviewed, open-access journal, which was founded in March 2012. TLCR is indexed by PubMed/PubMed Central and the Chemical Abstracts Service (CAS) Databases. It is published quarterly the first year, and published bimonthly since February 2013. It provides practical up-to-date information on prevention, early detection, diagnosis, and treatment of lung cancer. Specific areas of its interest include, but not limited to, multimodality therapy, markers, imaging, tumor biology, pathology, chemoprevention, and technical advances related to lung cancer.
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