Radiomics of Preoperative Multi-Sequence Magnetic Resonance Imaging Can Improve the Predictive Performance of Microvascular Invasion in Hepatocellular Carcinoma.

IF 2.1 Q3 ONCOLOGY
World Journal of Oncology Pub Date : 2024-02-01 Epub Date: 2023-12-09 DOI:10.14740/wjon1731
Wan Min Liu, Xing Yu Zhao, Meng Ting Gu, Kai Rong Song, Wei Zheng, Hui Yu, Hui Lin Chen, Xiao Wen Xu, Xiang Zhou, Ai E Liu, Ning Yang Jia, Pei Jun Wang
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引用次数: 0

Abstract

Background: The aim of the study is to demonstrate that radiomics of preoperative multi-sequence magnetic resonance imaging (MRI) can indeed improve the predictive performance of microvascular invasion (MVI) in hepatocellular carcinoma (HCC).

Methods: A total of 206 patients with pathologically confirmed HCC who underwent preoperative enhanced MRI were retrospectively recruited. Univariate and multivariate logistic regression analysis identified the independent clinicoradiologic predictors of MVI present and constituted the clinicoradiologic model. Recursive feature elimination (RFE) was applied to select radiomics features (extracted from six sequence images) and constructed the radiomics model. Clinicoradiologic model plus radiomics model formed the clinicoradiomics model. Five-fold cross-validation was used to validate the three models. Discrimination, calibration, and clinical utility were used to evaluate the performance. Net reclassification improvement (NRI) and integrated discrimination improvement (IDI) were used to compare the prediction accuracy between models.

Results: The clinicoradiologic model contained alpha-fetoprotein (AFP)_lg10, radiological capsule enhancement, enhancement pattern and arterial peritumoral enhancement, which were independent risk factors of MVI. There were 18 radiomics features related to MVI constructed the radiomics model. The mean area under the receiver operating curve (AUC) of clinicoradiologic, radiomics and clinicoradiomics model were 0.849, 0.925 and 0.950 in the training cohort and 0.846, 0.907 and 0.933 in the validation cohort, respectively. The three models' calibration curves fitted well, and decision curve analysis (DCA) confirmed the clinical usefulness. Compared with the clinicoradiologic model, the NRI of radiomics and clinicoradiomics model increased significantly by 0.575 and 0.825, respectively, and the IDI increased significantly by 0.280 and 0.398, respectively.

Conclusions: Radiomics of preoperative multi-sequence MRI can improve the predictive performance of MVI in HCC.

术前多序列磁共振成像的放射组学可提高肝细胞癌微血管侵犯的预测性能
背景:本研究旨在证明术前多序列磁共振成像(MRI)的放射组学确实可以提高肝细胞癌(HCC)微血管侵犯(MVI)的预测性能:方法:回顾性招募了206例经病理确诊的HCC患者,这些患者在术前接受了增强磁共振成像。单变量和多变量逻辑回归分析确定了出现 MVI 的独立临床放射学预测因素,并构成了临床放射学模型。递归特征消除(RFE)用于选择放射组学特征(从六幅序列图像中提取),并构建放射组学模型。临床放射学模型加上放射组学模型组成了临床放射组学模型。五倍交叉验证用于验证三个模型。使用判别、校准和临床实用性来评估其性能。净再分类改进(NRI)和综合判别改进(IDI)用于比较不同模型的预测准确性:临床放射学模型包含甲胎蛋白(AFP)_lg10、放射学胶囊强化、强化模式和瘤周动脉强化,它们是MVI的独立风险因素。共有18个与MVI相关的放射组学特征构建了放射组学模型。临床放射学模型、放射组学模型和临床放射学模型的平均接收操作曲线下面积(AUC)在训练队列中分别为0.849、0.925和0.950,在验证队列中分别为0.846、0.907和0.933。三个模型的校准曲线拟合良好,决策曲线分析(DCA)证实了其临床实用性。与临床放射学模型相比,放射组学和临床放射学模型的NRI分别显著增加了0.575和0.825,IDI分别显著增加了0.280和0.398:结论:术前多序列核磁共振成像的放射组学可提高HCC MVI的预测性能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
6.10
自引率
15.40%
发文量
37
期刊介绍: World Journal of Oncology, bimonthly, publishes original contributions describing basic research and clinical investigation of cancer, on the cellular, molecular, prevention, diagnosis, therapy and prognosis aspects. The submissions can be basic research or clinical investigation oriented. This journal welcomes those submissions focused on the clinical trials of new treatment modalities for cancer, and those submissions focused on molecular or cellular research of the oncology pathogenesis. Case reports submitted for consideration of publication should explore either a novel genomic event/description or a new safety signal from an oncolytic agent. The areas of interested manuscripts are these disciplines: tumor immunology and immunotherapy; cancer molecular pharmacology and chemotherapy; drug sensitivity and resistance; cancer epidemiology; clinical trials; cancer pathology; radiobiology and radiation oncology; solid tumor oncology; hematological malignancies; surgical oncology; pediatric oncology; molecular oncology and cancer genes; gene therapy; cancer endocrinology; cancer metastasis; prevention and diagnosis of cancer; other cancer related subjects. The types of manuscripts accepted are original article, review, editorial, short communication, case report, letter to the editor, book review.
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