18F-FDG PET/CT-based habitat radiomics combining stacking ensemble learning for predicting prognosis in hepatocellular carcinoma: a multi-center study.

IF 3.4 2区 医学 Q2 ONCOLOGY BMC Cancer Pub Date : 2024-11-27 DOI:10.1186/s12885-024-13206-5
Chunxiao Sui, Qian Su, Kun Chen, Rui Tan, Ziyang Wang, Zifan Liu, Wengui Xu, Xiaofeng Li
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Abstract

Background: This study aims to develop habitat radiomic models to predict overall survival (OS) for hepatocellular carcinoma (HCC), based on the characterization of the intratumoral heterogeneity reflected in 18F-FDG PET/CT images.

Methods: A total of 137 HCC patients from two institutions were retrospectively included. First, intratumoral habitats were achieved by a two-step unsupervised clustering process based on k-means clustering. Second, a total of 4032 radiomic features were extracted based on each habitat, including 2016 PET-based and 2016 CT-based radiomic features. Then, after feature selection, the stacking ensemble learning approach which combined six machine learning classifiers as the first-level learners with Cox proportional hazards regression as the second-level learner, was employed to build multiple radiomic models. Finally, the optimal model was selected based on the calculation of the C-index, and a combined model integrating with a clinical model was also constructed to identify the potentially complementary effect.

Results: Three spatially distinct habitats were identified in the two cohorts. Among a total of 30 stacking ensemble learning models established based on different combinations of 5 types of segmented volumes of interest (VOIs) with 6 types of classifiers, the MLP-Cox-habitat-2 model was selected as the optimal radiomic model with a C-index of 0.702 in the external validation cohort. Furthermore, the combined model integrating the optimal radiomic model with the clinical model achieved an improved C-index of 0.747. Consistently, the combined model outperformed the other models for OS prediction, with a time-dependent AUC of 0.835, 0.828, and 0.800 in the 1-year, 2-year, and 3-year OS, respectively.

Conclusion: 18F-FDG PET/CT-based habitat radiomics outperformed traditional radiomics in OS prediction for HCC, with a further improved predictive power by integrating with the clinical model. The optimal combined habitat model was potentially promising in guiding individualized treatment for HCC.

Trial registration: This study was a retrospective study, so it was free from registration.

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基于 18F-FDG PET/CT 的生境放射组学结合堆叠集合学习预测肝细胞癌的预后:一项多中心研究。
研究背景本研究旨在根据18F-FDG PET/CT图像所反映的瘤内异质性特征,开发预测肝细胞癌(HCC)总生存率(OS)的生境放射学模型:方法:回顾性纳入两家机构的 137 例 HCC 患者。首先,通过基于 k-means 聚类的两步无监督聚类过程实现了瘤内生境。其次,根据每个栖息地提取共 4032 个放射学特征,包括基于 PET 的 2016 个放射学特征和基于 CT 的 2016 个放射学特征。然后,在特征选择之后,采用堆叠集合学习方法,将六个机器学习分类器作为第一级学习器,将 Cox 比例危险回归作为第二级学习器,建立多个辐射组学模型。最后,根据 C 指数的计算结果选出最佳模型,并构建了一个与临床模型相结合的综合模型,以确定潜在的互补效应:结果:在两个队列中发现了三种不同的空间生境。在基于 5 种兴趣体积(VOI)分割与 6 种分类器的不同组合而建立的总共 30 个堆叠集合学习模型中,MLP-Cox-habitat-2 模型被选为外部验证队列中的最佳放射学模型,其 C 指数为 0.702。此外,整合了最佳放射学模型和临床模型的组合模型的 C 指数提高到了 0.747。结论:基于18F-FDG PET/CT的生境放射组学在预测HCC的OS方面优于传统的放射组学,与临床模型整合后,预测能力进一步提高。优化组合的生境模型在指导HCC的个体化治疗方面具有潜在的前景:本研究为回顾性研究,因此无需注册。
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来源期刊
BMC Cancer
BMC Cancer 医学-肿瘤学
CiteScore
6.00
自引率
2.60%
发文量
1204
审稿时长
6.8 months
期刊介绍: BMC Cancer is an open access, peer-reviewed journal that considers articles on all aspects of cancer research, including the pathophysiology, prevention, diagnosis and treatment of cancers. The journal welcomes submissions concerning molecular and cellular biology, genetics, epidemiology, and clinical trials.
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