4.7 Article

Utility of pre-treatment FDG PET/CT-derived machine learning models for outcome prediction in classical Hodgkin lymphoma

期刊

EUROPEAN RADIOLOGY
卷 32, 期 10, 页码 7237-7247

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SPRINGER
DOI: 10.1007/s00330-022-09039-0

关键词

Hodgkin disease: positron emission tomography computed tomography; Machine learning, progression-free survival

资金

  1. Innovate UK

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This study evaluated the ability of machine learning models derived from pre-treatment FDG PET/CT to predict outcomes in cHL patients. The results showed that a ridge regression model using a 1.5 x mean liver SUV segmentation had the highest performance, with a high AUC when evaluated on training, validation, and test datasets.
Objectives Relapse occurs in similar to 20% of patients with classical Hodgkin lymphoma (cHL) despite treatment adaption based on 2dcoxy-2[F-18]fluoro-D-glucose positron emission tomography/computed tomography response. The objective was to evaluate pre-treatment FDG PET/CT-derived machine learning (ML) models for predicting outcome in patients with cHL. Methods All cHL patients undergoing pre-treatment PET/CT at our institution between 2008 and 2018 were retrospectively identified. A 1.5 x mean liver standardised uptake value (SUV) and a fixed 4.0 SUV threshold were used to segment PET/CT data. Feature extraction was performed using PyRadiomics with ComBat harmonisation. Training (80%) and test (20%) cohorts stratified around 2-year event-free survival (EFS), age, sex, ethnicity and disease stage were defined. Seven ML models were trained and hyperparameters tuned using stratified 5-fold cross-validation. Area under the curve (AUC) from receiver operator characteristic analysis was used to assess performance. Results A total of 289 patients (153 males), median age 36 (range 16-88 years), were included. There was no significant difference between training (n = 231) and test cohorts (n = 58) (p value > 0.05). A ridge regression model using a 1.5 x mean liver SUV segmentation had the highest performance, with mean training, validation and test AUCs of 0.82 +/- 0.002, 0.79 +/- 0.01 and 0.81 4- 0.12. However, there was no significant difference between a logistic model derived from metabolic tumour volume and clinical features or the highest performing radiomic model. Conclusions Outcome prediction using pre-treatment FDG PET/CT-derived ML models is feasible in cHL patients. Further work is needed to determine optimum predictive thresholds for clinical use.

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