各种恶性肿瘤组织学亚型和解剖学疾病起源的[18F]FDG PET/CT 放射组学分类器:原理验证研究

Cancers Pub Date : 2024-05-15 DOI:10.3390/cancers16101873
R. Hinzpeter, S. A. Mirshahvalad, Vanessa Murad, Lisa Avery, R. Kulanthaivelu, A. Kohan, C. Ortega, E. Elimova, Jonathan Yeung, A. Hope, U. Metser, P. Veit-Haibach
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摘要

我们的目的是研究[18F]F-FDG-PET/CT衍生放射组学能否对组织学亚型进行分类,并确定各种恶性肿瘤的解剖起源。在这项经 IRB 批准的回顾性研究中,共纳入了 391 名肺部恶性肿瘤(142 人)、胃食管恶性肿瘤(128 人)和头颈部恶性肿瘤(121 人)患者(年龄 = 66.7 ± 11.2)。图像分割和特征提取均以半自动方式进行。采用两种模型(所有可能子集回归[APS]和递归分割)预测组织学(鳞状细胞癌[SCC;n = 219]与腺癌[AC;n = 172])、解剖起源和组织学加解剖起源。递归分区算法在确定组织学方面优于 APS(灵敏度为 0.90 vs. 0.73;特异度为 0.77 vs. 0.65)。递归分区算法对解剖学来源也有很好的预测能力。尤其是肺部恶性肿瘤的识别准确率很高(灵敏度为 0.93;特异性为 0.98)。最后,组织学和解剖学疾病起源同步预测模型在确定胃食管癌(灵敏度 0.88;特异度 0.92)、肺癌(灵敏度 0.89;特异度 0.88)和头颈部 SCC(灵敏度 0.91;特异度 0.92)方面具有很高的准确性。在APS模型中,增加PET特征对组织学和起源的预测均有边际递增价值。总之,我们的研究表明,利用[18F]FDG-PET/CT衍生的放射组学特征(主要来自CT)来确定患者的组织学和解剖起源具有良好的预测能力。
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The [18F]F-FDG PET/CT Radiomics Classifier of Histologic Subtypes and Anatomical Disease Origins across Various Malignancies: A Proof-of-Principle Study
We aimed to investigate whether [18F]F-FDG-PET/CT-derived radiomics can classify histologic subtypes and determine the anatomical origin of various malignancies. In this IRB-approved retrospective study, 391 patients (age = 66.7 ± 11.2) with pulmonary (n = 142), gastroesophageal (n = 128) and head and neck (n = 121) malignancies were included. Image segmentation and feature extraction were performed semi-automatically. Two models (all possible subset regression [APS] and recursive partitioning) were employed to predict histology (squamous cell carcinoma [SCC; n = 219] vs. adenocarcinoma [AC; n = 172]), the anatomical origin, and histology plus anatomical origin. The recursive partitioning algorithm outperformed APS to determine histology (sensitivity 0.90 vs. 0.73; specificity 0.77 vs. 0.65). The recursive partitioning algorithm also revealed good predictive ability regarding anatomical origin. Particularly, pulmonary malignancies were identified with high accuracy (sensitivity 0.93; specificity 0.98). Finally, a model for the synchronous prediction of histology and anatomical disease origin resulted in high accuracy in determining gastroesophageal AC (sensitivity 0.88; specificity 0.92), pulmonary AC (sensitivity 0.89; specificity 0.88) and head and neck SCC (sensitivity 0.91; specificity 0.92). Adding PET-features was associated with marginal incremental value for both the prediction of histology and origin in the APS model. Overall, our study demonstrated a good predictive ability to determine patients’ histology and anatomical origin using [18F]F-FDG-PET/CT-derived radiomics features, mainly from CT.
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