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Dual-center validation of using magnetic resonance imaging radiomics to predict stereotactic radiosurgery outcomes.
DeVries, David A; Tang, Terence; Alqaidy, Ghada; Albweady, Ali; Leung, Andrew; Laba, Joanna; Lagerwaard, Frank; Zindler, Jaap; Hajdok, George; Ward, Aaron D.
Afiliación
  • DeVries DA; Department of Medical Biophysics, Western University, London, ON, Canada.
  • Tang T; Gerald C. Baines Centre, London Health Sciences Centre, London, ON, Canada.
  • Alqaidy G; Department of Radiation Oncology, London Regional Cancer Program, London, ON, Canada.
  • Albweady A; Radiodiagnostic and Medical Imaging Department, King Fahad Armed Forces Hospital, Jeddah, Saudi Arabia.
  • Leung A; Department of Radiology, Unaizah College of Medicine and Medical Sciences, Qassim University, Unaizah, Saudi Arabia.
  • Laba J; Department of Medical Imaging, Western University, London, ON, Canada.
  • Lagerwaard F; Department of Radiation Oncology, London Regional Cancer Program, London, ON, Canada.
  • Zindler J; Department of Oncology, Western University, London, ON, Canada.
  • Hajdok G; Department of Radiation Oncology, Amsterdam University Medical Centre, Amsterdam, The Netherlands.
  • Ward AD; Department of Radiation Oncology, Haaglanden Medical Centre, Den Haag, The Netherlands.
Neurooncol Adv ; 5(1): vdad064, 2023.
Article en En | MEDLINE | ID: mdl-37358938
ABSTRACT

Background:

MRI radiomic features and machine learning have been used to predict brain metastasis (BM) stereotactic radiosurgery (SRS) outcomes. Previous studies used only single-center datasets, representing a significant barrier to clinical translation and further research. This study, therefore, presents the first dual-center validation of these techniques.

Methods:

SRS datasets were acquired from 2 centers (n = 123 BMs and n = 117 BMs). Each dataset contained 8 clinical features, 107 pretreatment T1w contrast-enhanced MRI radiomic features, and post-SRS BM progression endpoints determined from follow-up MRI. Random decision forest models were used with clinical and/or radiomic features to predict progression. 250 bootstrap repetitions were used for single-center experiments.

Results:

Training a model with one center's dataset and testing it with the other center's dataset required using a set of features important for outcome prediction at both centers, and achieved area under the receiver operating characteristic curve (AUC) values up to 0.70. A model training methodology developed using the first center's dataset was locked and externally validated with the second center's dataset, achieving a bootstrap-corrected AUC of 0.80. Lastly, models trained on pooled data from both centers offered balanced accuracy across centers with an overall bootstrap-corrected AUC of 0.78.

Conclusions:

Using the presented validated methodology, radiomic models trained at a single center can be used externally, though they must utilize features important across all centers. These models' accuracies are inferior to those of models trained using each individual center's data. Pooling data across centers shows accurate and balanced performance, though further validation is required.
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Texto completo: 1 Colección: 01-internacional Tipo de estudio: Prognostic_studies / Risk_factors_studies Idioma: En Revista: Neurooncol Adv Año: 2023 Tipo del documento: Article País de afiliación: Canadá

Texto completo: 1 Colección: 01-internacional Tipo de estudio: Prognostic_studies / Risk_factors_studies Idioma: En Revista: Neurooncol Adv Año: 2023 Tipo del documento: Article País de afiliación: Canadá