Cheng Sihang, Hu Ge, Zhang Shenbo, Lv Rui, Sun Limeng, Zhang Zhe, Jin Zhengyu, Wu Yanyan, Huang Chen, Ye Lu, Feng Yunlu, Chen Zhe-Sheng, Wang Zhiwei, Xue Huadan, Yang Aiming
Department of Radiology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, Beijing, 100730, China.
Theranostics and Translational Research Center, National Infrastructures for Translational Medicine, Institute of Clinical Medicine, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100730, China.
Adv Sci (Weinh). 2025 May;12(20):e2409488. doi: 10.1002/advs.202409488. Epub 2025 Apr 28.
The malignant potential of pancreatic cystic lesions (PCLs) varies dramatically, leading to difficulties when making clinical decisions. This study aimed to develop noninvasive clinical-radiomic models using preoperative CT images to predict the malignant potential of PCLs. It also investigates the biological mechanisms underlying these models. Patients from two retrospective and one prospective cohort, all undergoing surgical resection for PCLs, are divided into four datasets: training, internal test, external test, and prospective application sets. Eleven machine learning classifiers are employed to construct radiomic models based on selected features. Cyst fluid from the prospective cohort is collected for proteomic and lipidomic analysis. The radiomic models demonstrated high accuracy, with area under the receiver operating characteristic curves (AUCs) > 0.93 across the training (n = 262), internal test (n = 50), and external test (n = 50) sets. AUCs ranged from 0.92 to 0.96 for the prospective cohort (n = 34). Meanwhile, differentially-expressed proteins and lipid molecules, along with their associated signaling pathways, are identified between high and low groups of clinical-radiomic scores. This models can effectively and accurately predict the malignant potential of PCLs, with multi-omics evidence suggesting the biological mechanisms involving secretion function and lipid metabolism underlying clinical-radiomic models.
胰腺囊性病变(PCLs)的恶性潜能差异很大,这给临床决策带来了困难。本研究旨在利用术前CT图像开发非侵入性临床-影像组学模型,以预测PCLs的恶性潜能。同时还研究了这些模型背后的生物学机制。来自两个回顾性队列和一个前瞻性队列的患者,均因PCLs接受手术切除,被分为四个数据集:训练集、内部测试集、外部测试集和前瞻性应用集。使用11种机器学习分类器,基于选定特征构建影像组学模型。收集前瞻性队列的囊液进行蛋白质组学和脂质组学分析。影像组学模型表现出高准确性,在训练集(n = 262)、内部测试集(n = 50)和外部测试集(n = 50)中,受试者操作特征曲线下面积(AUCs)> 0.93。在前瞻性队列(n = 34)中,AUCs范围为0.92至0.96。同时,在临床-影像组学评分的高分组和低分组之间,鉴定出差异表达的蛋白质和脂质分子及其相关信号通路。该模型能够有效且准确地预测PCLs的恶性潜能,多组学证据表明临床-影像组学模型背后涉及分泌功能和脂质代谢的生物学机制。