Predicting T-Cell Lymphoma in Children From 18F-FDG PET-CT Imaging With Multiple Machine Learning Models.

This study aimed to examine the feasibility of utilizing radiomics models derived from 18F-FDG PET/CT imaging to screen for T-cell lymphoma in children with lymphoma. All patients had undergone 18F-FDG PET/CT scans. Lesions were extracted from PET/CT and randomly divided into training and validation...

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Publicado en:Journal of Digital Imaging Vol. 37; no. 3; pp. 952 - 965
Autores principales: Yang, Taiyu, Liu, Danyan, Zhang, Zexu, Sa, Ri, Guan, Feng
Formato: diagnostic images research tables/charts Journal Article
Publicado: Springer Nature Jun2024
Acceso en línea:Ver este registro en EBSCOhost
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      dt: Jun2024
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      pub: Springer Nature
      place: New York, New York
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        10.1007/s10278-024-01007-y
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        atl: Predicting T-Cell Lymphoma in Children From 18F-FDG PET-CT Imaging With Multiple Machine Learning Models.
      aug:
        au:
          Yang, Taiyu
          Liu, Danyan
          Zhang, Zexu
          Sa, Ri
          Guan, Feng
        affil: https://ror.org/034haf133 Department of Nuclear Medicine, The First Hospital of Jilin University, 1# Xinmin St, 130021, Changchun, China
      sug:
        subj:
          Lymphoma, T-Cell Radiography
          Fludeoxyglucose F 18 Diagnostic Use
          Cancer Screening
          Radiographic Image Interpretation, Computer-Assisted
          Machine Learning
          Prediction Models
          Radiomics
          Human
          Child
          Comparative Studies
          Validation Studies
          Funding Source
          Tomography, X-Ray Computed
          Random Assignment
          Logistic Regression
          Support Vector Machine
          Neural Networks (Computer)
          Descriptive Statistics
          Childhood Neoplasms Radiography
          Child: 6-12 years
      ab: This study aimed to examine the feasibility of utilizing radiomics models derived from 18F-FDG PET/CT imaging to screen for T-cell lymphoma in children with lymphoma. All patients had undergone 18F-FDG PET/CT scans. Lesions were extracted from PET/CT and randomly divided into training and validation sets. Two different types of models were constructed as follows: features that are extracted from standardized uptake values (SUV)-associated parameters, and CT images were used to build SUV/CT-based model. Features that are derived from PET and CT images were used to build PET/CT-based model. Logistic regression (LR), linear support vector machine, support vector machine with the radial basis function kernel, neural networks, and adaptive boosting were performed as classifiers in each model. In the training sets, 77 patients, and 247 lesions were selected for building the models. In the validation sets, PET/CT-based model demonstrated better performance than that of SUV/CT-based model in the prediction of T-cell lymphoma. LR showed highest accuracy with 0.779 [0.697, 0.860], area under the receiver operating characteristic curve (AUC) with 0.863 [0.762, 0.963], and preferable goodness-of-fit in PET/CT-based model at the patient level. LR also showed best performance with accuracy of 0.838 [0.741, 0.936], AUC of 0.907 [0.839, 0.976], and preferable goodness-of-fit in PET/CT-based model at the lesion level. 18F-FDG PET/CT-based radiomics models with different machine learning classifiers were able to screen T-cell lymphoma in children with high accuracy, AUC, and preferable goodness-of-fit, providing incremental value compared with SUV-associated features.
      pubtype: Academic Journal
      doctype:
        diagnostic images
        research
        tables/charts
        Journal Article
      ougenre: Article
    language: English
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