Distinguishing lymphoma from benign lymph node diseases in fever of unknown origin using PET/CT radiomics.

IF 3.1 3区 医学 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING EJNMMI Research Pub Date : 2024-11-13 DOI:10.1186/s13550-024-01171-w
Xinchao Zhang, Fenglian Jing, Yujing Hu, Congna Tian, Jianyang Zhang, Shuheng Li, Qiang Wei, Kang Li, Lu Zheng, Jiale Liu, Jingjie Zhang, Yanzhu Bian
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Abstract

Background: A considerable portion of patients with fever of unknown origin (FUO) present concomitant lymphadenopathy. Diseases within the spectrum of FUO accompanied by lymphadenopathy include lymphoma, infections, and rheumatic diseases. Particularly, lymphoma has emerged as the most prevalent etiology of FUO with associated lymphadenopathy. Distinguishing between benign and malignant lymph node lesions is a major challenge for physicians and an urgent clinical concern for patients. However, conventional imaging techniques, including PET/CT, often have difficulty accurately distinguishing between malignant and benign lymph node lesions. This study utilizes PET/CT radiomics to differentiate between lymphoma and benign lymph node lesions in patients with FUO, aiming to improve diagnostic accuracy.

Results: Data were collected from 204 patients who underwent 18F-FDG PET/CT examinations for FUO, including 114 lymphoma patients and 90 patients with benign lymph node lesions. Patients were randomly divided into training and testing groups at a ratio of 7:3. A total of 15 effective features were obtained by the least absolute shrinkage and selection operator (LASSO) algorithm. Machine learning models were constructed using logistic regression (LR), support vector machine (SVM), random forest (RF), and k-nearest neighbors (KNN) algorithms. In the training group, the area under the curve (AUC) values for predicting lymphoma and benign cases by LR, SVM, RF, and KNN models were 0.936, 0.930, 0.998, and 0.938, respectively. There were statistically significant differences in AUC between the RF and other models (all P < 0.001). In the testing group, the AUC values for the four models were 0.860, 0.866, 0.915, and 0.891, respectively, with no statistically significant differences observed among them (all P > 0.05). The decision curve analysis (DCA) curves of the RF model outperformed those of the other three models in both the training and testing groups.

Conclusions: PET/CT radiomics demonstrated promising performance in discriminating lymphoma from benign lymph node lesions in patients with FUO, with the RF model showing the best performance.

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利用 PET/CT 放射线组学区分不明原因发热中的淋巴瘤和良性淋巴结疾病。
背景:相当一部分不明原因发热(FUO)患者会伴有淋巴结病。FUO 伴有淋巴结病的疾病包括淋巴瘤、感染和风湿病。尤其是淋巴瘤已成为伴有淋巴结病的 FUO 的最常见病因。如何区分良性和恶性淋巴结病变是医生面临的一大挑战,也是患者急需解决的临床问题。然而,包括 PET/CT 在内的传统成像技术往往难以准确区分恶性和良性淋巴结病变。本研究利用PET/CT放射组学来区分FUO患者的淋巴瘤和良性淋巴结病变,旨在提高诊断的准确性:研究收集了204名接受18F-FDG PET/CT检查的FUO患者的数据,其中包括114名淋巴瘤患者和90名良性淋巴结病变患者。患者按 7:3 的比例随机分为训练组和测试组。通过最小绝对收缩和选择算子(LASSO)算法共获得 15 个有效特征。使用逻辑回归(LR)、支持向量机(SVM)、随机森林(RF)和k-近邻(KNN)算法构建了机器学习模型。在训练组中,LR、SVM、RF 和 KNN 模型预测淋巴瘤和良性病例的曲线下面积(AUC)值分别为 0.936、0.930、0.998 和 0.938。RF 模型与其他模型的 AUC 差异有统计学意义(均为 P 0.05)。在训练组和测试组中,RF 模型的决策曲线分析(DCA)曲线均优于其他三种模型:PET/CT放射组学在鉴别FUO患者淋巴瘤和良性淋巴结病变方面表现良好,其中RF模型表现最佳。
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来源期刊
EJNMMI Research
EJNMMI Research RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING&nb-
CiteScore
5.90
自引率
3.10%
发文量
72
审稿时长
13 weeks
期刊介绍: EJNMMI Research publishes new basic, translational and clinical research in the field of nuclear medicine and molecular imaging. Regular features include original research articles, rapid communication of preliminary data on innovative research, interesting case reports, editorials, and letters to the editor. Educational articles on basic sciences, fundamental aspects and controversy related to pre-clinical and clinical research or ethical aspects of research are also welcome. Timely reviews provide updates on current applications, issues in imaging research and translational aspects of nuclear medicine and molecular imaging technologies. The main emphasis is placed on the development of targeted imaging with radiopharmaceuticals within the broader context of molecular probes to enhance understanding and characterisation of the complex biological processes underlying disease and to develop, test and guide new treatment modalities, including radionuclide therapy.
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