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Deep transfer learning-based prostate cancer classification using 3 Tesla multi-parametric MRI.

Xinran Zhong1,2, Ruiming Cao3,4, Sepideh Shakeri3

  • 1Department of Radiological Sciences, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, USA. XZhong@mednet.ucla.edu.

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|November 22, 2018
PubMed
Summary
This summary is machine-generated.

A deep transfer learning (DTL) model effectively distinguishes indolent from significant prostate cancer (PCa) on MRI, showing improved accuracy over standard deep learning and PIRADS v2 scoring. This DTL approach enhances PCa lesion classification in clinical practice.

Keywords:
Clinically significant lesion classificationDeep learningMulti-parametric MRIPIRADS v2 scoreProstate cancerWhole-mount histopathology

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Area of Science:

  • Radiology
  • Artificial Intelligence
  • Oncology

Background:

  • Prostate cancer (PCa) detection and classification are crucial for patient management.
  • Accurate differentiation between indolent and clinically significant PCa on MRI is challenging.
  • Current methods like PIRADS v2 scoring have limitations in distinguishing PCa aggressiveness.

Purpose of the Study:

  • To develop and evaluate a deep transfer learning (DTL) model for differentiating indolent from clinically significant prostate cancer (PCa) lesions.
  • To compare the performance of the DTL model against a conventional deep learning (DL) model and the PIRADS v2 score.
  • To validate the models using whole-mount histopathology (WMHP) on 3 Tesla multi-parametric MRI (3T mp-MRI).

Main Methods:

  • A cohort of 140 patients with 3T mp-MRI and WMHP was studied.
  • A DTL-based model was trained on 169 lesions from 110 patients and tested on 47 lesions from 30 patients.
  • Performance was assessed using accuracy, sensitivity, specificity, and area under the curve (AUC), with comparisons to a DL model without transfer learning and PIRADS v2 score (≥4).

Main Results:

  • The DTL-based model achieved an AUC of 0.726, outperforming the DL model (AUC 0.687) and PIRADS v2 score (AUC 0.711) in discriminating clinically significant PCa lesions.
  • The DTL model demonstrated superior performance in identifying significant PCa lesions in the testing set.
  • The DTL model's AUC was comparable to the PIRADS v2 score (p=0.89).

Conclusions:

  • The proposed DTL-based model shows promise for improving the classification of prostate cancer lesions on 3T mp-MRI.
  • DTL offers a potential advancement over standard DL techniques and PIRADS v2 scoring for PCa aggressiveness assessment.
  • Further validation is warranted to integrate this DTL model into routine clinical practice for enhanced PCa diagnosis.