David Grajales, William T Le, Victor Blanquez-Yeste, Frédérick Dallaire, Feryel Azzi, Guila Delouya, Dominique Trudel, Frédéric Leblond, Cynthia Ménard, Samuel Kadoury
{"title":"Deployment of a real-time prostate cancer confirmation system with Raman spectroscopy: fine-tuning versus test-time adaptation of 1D CNNs.","authors":"David Grajales, William T Le, Victor Blanquez-Yeste, Frédérick Dallaire, Feryel Azzi, Guila Delouya, Dominique Trudel, Frédéric Leblond, Cynthia Ménard, Samuel Kadoury","doi":"10.1117/1.BIOS.2.3.032706","DOIUrl":null,"url":null,"abstract":"<p><strong>Significance: </strong>Prostate cancer (PCa) confirmation during needle-based procedures is limited by the lack of intraoperative diagnostic tools. Raman spectroscopy (RS), combined with classification models, offers a promising solution for real-time tissue characterization, potentially improving sampling accuracy and therapy guidance. However, such models require tissue- and organ-specific data, making deployment in studies challenging due to limited data availability.</p><p><strong>Aim: </strong>The aim is to develop a one-dimensional convolutional neural network (1D-CNN) for real-time PCa detection using RS on prospectively collected <i>ex vivo</i> data, leveraging multi-organ pre-training and evaluating two domain adaptation strategies.</p><p><strong>Approach: </strong>A ResNet-based 1D-CNN was trained for binary cancer/normal tissue classification. We implemented a pre-training strategy using retrospective RS data from brain, breast, and prostate (202 patients), along with pre-trained bacterial models, followed by efficient fine-tuning and test-time adaptation (TTA) to adapt to unseen domains.</p><p><strong>Results: </strong>Prospective RS data were acquired using a robotic system from 10 PCa patients (two to five biopsies each). The fine-tuned model achieved 0.76 area under the receiver operating characteristic curve, 0.79 accuracy, 0.83 sensitivity, and 0.72 specificity, outperforming support vector machines. TTA improved predictions when labels were unavailable.</p><p><strong>Conclusions: </strong>Pre-trained 1D-CNNs combined with efficient fine-tuning or TTA enable accurate PCa detection in small-cohort settings using real-time RS.</p>","PeriodicalId":519981,"journal":{"name":"Biophotonics discovery","volume":"2 3","pages":"032706"},"PeriodicalIF":0.0000,"publicationDate":"2025-09-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13052485/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biophotonics discovery","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1117/1.BIOS.2.3.032706","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/7/1 0:00:00","PubModel":"eCollection","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Significance: Prostate cancer (PCa) confirmation during needle-based procedures is limited by the lack of intraoperative diagnostic tools. Raman spectroscopy (RS), combined with classification models, offers a promising solution for real-time tissue characterization, potentially improving sampling accuracy and therapy guidance. However, such models require tissue- and organ-specific data, making deployment in studies challenging due to limited data availability.
Aim: The aim is to develop a one-dimensional convolutional neural network (1D-CNN) for real-time PCa detection using RS on prospectively collected ex vivo data, leveraging multi-organ pre-training and evaluating two domain adaptation strategies.
Approach: A ResNet-based 1D-CNN was trained for binary cancer/normal tissue classification. We implemented a pre-training strategy using retrospective RS data from brain, breast, and prostate (202 patients), along with pre-trained bacterial models, followed by efficient fine-tuning and test-time adaptation (TTA) to adapt to unseen domains.
Results: Prospective RS data were acquired using a robotic system from 10 PCa patients (two to five biopsies each). The fine-tuned model achieved 0.76 area under the receiver operating characteristic curve, 0.79 accuracy, 0.83 sensitivity, and 0.72 specificity, outperforming support vector machines. TTA improved predictions when labels were unavailable.
Conclusions: Pre-trained 1D-CNNs combined with efficient fine-tuning or TTA enable accurate PCa detection in small-cohort settings using real-time RS.