基于18F-FDG PET-CT及临床因素的放疗组学预测结直肠癌淋巴血管侵袭的术前研究

Yan Yang, Huanhuan Wei, Fangfang Fu, Wei Wei, Yaping Wu, Yan Bai, Qing Li, Meiyun Wang
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引用次数: 0

摘要

目的:本研究的目的是探讨基于正电子发射断层扫描-计算机断层扫描(PET-CT)放射组学特征结合淋巴血管侵袭(LVI)临床预测因子的临床放射组学模型在预测结直肠癌(CRC)患者术前LVI中的价值。方法:回顾性分析95例术前行18f -氟脱氧葡萄糖(FDG) PET-CT检查的结直肠癌患者。采用单因素和多因素logistic回归分析,分析LVI阳性和LVI阴性组的临床因素和PET代谢数据,以确定LVI的独立预测因素。我们基于放射组学特征和临床数据构建了四个预测模型来预测LVI状态。根据受试者工作特征曲线评价不同模型的预测效果。构建最佳模型的模态图,并采用标定曲线和临床决策曲线对其性能进行评价。结果:平均标准化摄取值(SUVmean)、最大肿瘤直径和淋巴结转移是结直肠癌患者LVI的独立预测因子(P > 0.05)。结论:本研究构建的临床放射组学预测模型对CRC患者LVI术前个体化预测具有较高的应用价值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Preoperative prediction of lymphovascular invasion of colorectal cancer by radiomics based on 18F-FDG PET-CT and clinical factors.

Preoperative prediction of lymphovascular invasion of colorectal cancer by radiomics based on 18F-FDG PET-CT and clinical factors.

Preoperative prediction of lymphovascular invasion of colorectal cancer by radiomics based on 18F-FDG PET-CT and clinical factors.

Preoperative prediction of lymphovascular invasion of colorectal cancer by radiomics based on 18F-FDG PET-CT and clinical factors.

Purpose: The purpose of this study was to investigate the value of a clinical radiomics model based on Positron emission tomography-computed tomography (PET-CT) radiomics features combined with clinical predictors of Lymphovascular invasion (LVI) in predicting preoperative LVI in patients with colorectal cancer (CRC).

Methods: A total of 95 CRC patients who underwent preoperative 18F-fluorodeoxyglucose (FDG) PET-CT examination were retrospectively enrolled. Univariate and multivariate logistic regression analyses were used to analyse clinical factors and PET metabolic data in the LVI-positive and LVI-negative groups to identify independent predictors of LVI. We constructed four prediction models based on radiomics features and clinical data to predict LVI status. The predictive efficacy of different models was evaluated according to the receiver operating characteristic curve. Then, the nomogram of the best model was constructed, and its performance was evaluated using calibration and clinical decision curves.

Results: Mean standardized uptake value (SUVmean), maximum tumour diameter and lymph node metastasis were independent predictors of LVI in CRC patients (P < 0.05). The clinical radiomics model obtained the best prediction performance, with an Area Under Curve (AUC) of 0.922 (95%CI 0.820-0.977) and 0.918 (95%CI 0.782-0.982) in the training and validation cohorts, respectively. A nomogram based on the clinical radiomics model was constructed, and the calibration curve fitted well (P > 0.05).

Conclusion: The clinical radiomics prediction model constructed in this study has high value in the preoperative individualized prediction of LVI in CRC patients.

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