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Impact of Scanner Manufacturer, Endorectal Coil Use, and Clinical Variables on Deep Learning-assisted Prostate Cancer

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Summary

Scanner manufacturer and scanning protocol significantly impact deep learning model performance for classifying prostate cancer (PCa) aggressiveness on biparametric MRI (bpMRI). Model performance was higher when trained and tested on data from the same manufacturer.

Keywords:
Computer Applications–General (Informatics)Computer-aided Diagnosis (CAD)Convolutional Neural Network (CNN)Oncology

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Area of Science:

  • Medical Imaging Informatics
  • Artificial Intelligence in Oncology
  • Radiomics and Machine Learning

Background:

  • Accurate classification of prostate cancer (PCa) aggressiveness is crucial for treatment decisions.
  • Deep learning (DL) models show promise for analyzing biparametric MRI (bpMRI) in PCa detection.
  • The generalizability of DL models is often limited by variations in imaging hardware and protocols.

Purpose of the Study:

  • To evaluate the influence of scanner manufacturer and scanning protocol on DL model performance for PCa aggressiveness classification using bpMRI.
  • To assess the impact of data from different subgroups, including scanner manufacturers and endorectal coil (ERC) use, on model generalizability.
  • To determine if clinical features improve DL model performance in PCa aggressiveness assessment.

Main Methods:

  • Retrospective analysis of 5478 PCa bpMRI cases from the ProstateNet dataset across 13 centers.
  • Development and testing of five DL models to predict PCa aggressiveness using minimal lesion information.
  • Evaluation of model performance using area under the receiver operating characteristic curve (AUC), comparing performance across different scanner manufacturers (Siemens, Philips, GE) and ERC usage.

Main Results:

  • The best DL model achieved an AUC of 0.73 when trained and tested on the full dataset.
  • Models demonstrated higher performance when trained and tested on data from the same manufacturer (average AUC difference of 0.05, P < .001).
  • Inclusion of clinical features (age, PSA, PI-RADS) did not significantly improve model performance (P = .24).

Conclusions:

  • Scanner manufacturer and ERC use significantly affect the performance and feature distributions of DL models for automated PCa aggressiveness classification on bpMRI.
  • Model generalizability is challenged by variations in imaging acquisition parameters.
  • Future DL model development for PCa classification requires careful consideration of multi-center and multi-manufacturer data harmonization.