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A Weakly Supervised Deep Learning Method for Guiding Ovarian Cancer Treatment and Identifying an Effective Biomarker.
Wang, Ching-Wei; Lee, Yu-Ching; Chang, Cheng-Chang; Lin, Yi-Jia; Liou, Yi-An; Hsu, Po-Chao; Chang, Chun-Chieh; Sai, Aung-Kyaw-Oo; Wang, Chih-Hung; Chao, Tai-Kuang.
Affiliation
  • Wang CW; Graduate Institute of Biomedical Engineering, National Taiwan University of Science and Technology, Taipei 106335, Taiwan.
  • Lee YC; Graduate Institute of Applied Science and Technology, National Taiwan University of Science and Technology, Taipei 106335, Taiwan.
  • Chang CC; Graduate Institute of Applied Science and Technology, National Taiwan University of Science and Technology, Taipei 106335, Taiwan.
  • Lin YJ; Department of Gynecology and Obstetrics, Tri-Service General Hospital, Taipei 11490, Taiwan.
  • Liou YA; Graduate Institute of Medical Sciences, National Defense Medical Center, Taipei 11490, Taiwan.
  • Hsu PC; Department of Pathology, Tri-Service General Hospital, Taipei 11490, Taiwan.
  • Chang CC; Institute of Pathology and Parasitology, National Defense Medical Center, Taipei 11490, Taiwan.
  • Sai AK; Graduate Institute of Biomedical Engineering, National Taiwan University of Science and Technology, Taipei 106335, Taiwan.
  • Wang CH; Department of Gynecology and Obstetrics, Tri-Service General Hospital, Taipei 11490, Taiwan.
  • Chao TK; Graduate Institute of Medical Sciences, National Defense Medical Center, Taipei 11490, Taiwan.
Cancers (Basel) ; 14(7)2022 Mar 24.
Article in En | MEDLINE | ID: mdl-35406422
ABSTRACT
Ovarian cancer is a common malignant gynecological disease. Molecular target therapy, i.e., antiangiogenesis with bevacizumab, was found to be effective in some patients of epithelial ovarian cancer (EOC). Although careful patient selection is essential, there are currently no biomarkers available for routine therapeutic usage. To the authors' best knowledge, this is the first automated precision oncology framework to effectively identify and select EOC and peritoneal serous papillary carcinoma (PSPC) patients with positive therapeutic effect. From March 2013 to January 2021, we have a database, containing four kinds of immunohistochemical tissue samples, including AIM2, c3, C5 and NLRP3, from patients diagnosed with EOC and PSPC and treated with bevacizumab in a hospital-based retrospective study. We developed a hybrid deep learning framework and weakly supervised deep learning models for each potential biomarker, and the experimental results show that the proposed model in combination with AIM2 achieves high accuracy 0.92, recall 0.97, F-measure 0.93 and AUC 0.97 for the first experiment (66% training and 34%testing) and high accuracy 0.86 ± 0.07, precision 0.9 ± 0.07, recall 0.85 ± 0.06, F-measure 0.87 ± 0.06 and AUC 0.91 ± 0.05 for the second experiment using five-fold cross validation, respectively. Both Kaplan-Meier PFS analysis and Cox proportional hazards model analysis further confirmed that the proposed AIM2-DL model is able to distinguish patients gaining positive therapeutic effects with low cancer recurrence from patients with disease progression after treatment (p < 0.005).
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Observational_studies Language: En Journal: Cancers (Basel) Year: 2022 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Observational_studies Language: En Journal: Cancers (Basel) Year: 2022 Document type: Article Affiliation country: