Clinically Significant Prostate Cancer Prediction Using Multimodal Deep Learning with Prostate-Specific Antigen Restriction.

Journal: Current oncology (Toronto, Ont.)
Published Date:

Abstract

Prostate cancer (PCa) is a clinically heterogeneous disease. Predicting clinically significant PCa with low-intermediate prostate-specific antigen (PSA), which often includes aggressive cancers, is imperative. This study evaluated the predictive accuracy of deep learning analysis using multimodal medical data focused on clinically significant PCa in patients with PSA ≤ 20 ng/mL. Our cohort study included 178 consecutive patients who underwent ultrasound-guided prostate biopsy. Deep learning analyses were applied to predict clinically significant PCa. We generated receiver operating characteristic curves and calculated the corresponding area under the curve (AUC) to assess the prediction. The AUC of the integrated medical data using our multimodal deep learning approach was 0.878 (95% confidence interval [CI]: 0.772-0.984) in all patients without PSA restriction. Despite the reduced predictive ability of PSA when restricted to PSA ≤ 20 ng/mL ( = 122), the AUC was 0.862 (95% CI: 0.723-1.000), complemented by imaging data. In addition, we assessed clinical presentations and images belonging to representative false-negative and false-positive cases. Our multimodal deep learning approach assists physicians in determining treatment strategies by predicting clinically significant PCa in patients with PSA ≤ 20 ng/mL before biopsy, contributing to personalized medical workflows for PCa management.

Authors

  • Hayato Takeda
    Department of Urology, Nippon Medical School Hospital, Tokyo 113-8603, Japan. s8053@nms.ac.jp.
  • Jun Akatsuka
    Pathology Informatics Team, RIKEN Center for Advanced Intelligence Project, Tokyo 103-0027, Japan. jun.akatsuka@riken.jp.
  • Tomonari Kiriyama
    Department of Radiology, Nippon Medical School Hospital, Tokyo 113-8603, Japan.
  • Yuka Toyama
    Department of Urology, Nippon Medical School, Tokyo, Japan.
  • Yasushi Numata
    Pathology Informatics Team, RIKEN Center for Advanced Intelligence Project, Tokyo 103-0027, Japan. yasushi.numata@riken.jp.
  • Hiromu Morikawa
    Pathology Informatics Team, RIKEN Center for Advanced Intelligence Project, Tokyo 103-0027, Japan. hiromu.morikawa@riken.jp.
  • Kotaro Tsutsumi
    Pathology Informatics Team, RIKEN Center for Advanced Intelligence Project, Tokyo 103-0027, Japan. ktsutsum@hs.uci.edu.
  • Mami Takadate
    Department of Urology, Nippon Medical School Hospital, Tokyo 113-8603, Japan.
  • Hiroya Hasegawa
    Department of Urology, Nippon Medical School Hospital, Tokyo 113-8603, Japan.
  • Hikaru Mikami
    Department of Urology, Nippon Medical School, Tokyo, Japan.
  • Kotaro Obayashi
    Department of Urology, Nippon Medical School Hospital, Tokyo 113-8603, Japan.
  • Yuki Endo
    Department of Urology, Nippon Medical School Hospital, Tokyo 113-8603, Japan. y-endo1@nms.ac.jp.
  • Takayuki Takahashi
    Department of UroOncology Saitama Medical University International Medical Center Saitama Japan.
  • Manabu Fukumoto
    Pathology Informatics Team, RIKEN Center for Advanced Intelligence Project, Tokyo 103-0027, Japan. manabu.fukumoto@riken.jp.
  • Ryuji Ohashi
    Department of Integrated Diagnostic Pathology, Nippon Medical School, Tokyo 113-8603, Japan.
  • Akira Shimizu
    Department of Analytic Human Pathology, Nippon Medical School, Tokyo 113-8602, Japan. ashimizu@nms.ac.jp.
  • Go Kimura
    Department of Urology, Nippon Medical School Hospital, Tokyo 113-8603, Japan. gokimura@nms.ac.jp.
  • Yukihiro Kondo
    Department of Urology, Nippon Medical School Hospital, Tokyo 113-8603, Japan. kondoy@nms.ac.jp.
  • Yoichiro Yamamoto
    Department of Pathology, Shinshu University School of Medicine, Nagano, Japan.