Establishing a Highly Accurate Circulating Tumor Cell Image Recognition System for Human Lung Cancer by Pre-Training on Lung Cancer Cell Lines
Background/Objectives: Circulating tumor cells (CTCs) are important biomarkers for predicting prognosis and evaluating treatment efficacy in cancer. We developed the “CTC-Chip” system based on microfluidics, enabling highly sensitive CTC detection and prognostic assessment in lung cancer and maligna...
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Published in | Cancers Vol. 17; no. 14; p. 2289 |
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Main Authors | , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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Switzerland
MDPI AG
09.07.2025
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ISSN | 2072-6694 2072-6694 |
DOI | 10.3390/cancers17142289 |
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Abstract | Background/Objectives: Circulating tumor cells (CTCs) are important biomarkers for predicting prognosis and evaluating treatment efficacy in cancer. We developed the “CTC-Chip” system based on microfluidics, enabling highly sensitive CTC detection and prognostic assessment in lung cancer and malignant pleural mesothelioma. However, the final identification and enumeration of CTCs require manual intervention, which is time-consuming, prone to human error, and necessitates the involvement of experienced medical professionals. Medical image recognition using machine learning can reduce workload and improve automation. However, CTCs are rare in clinical samples, limiting the training data available to construct a robust CTC image recognition system. In this study, we established a highly accurate artificial intelligence-based CTC recognition system by pre-training convolutional neural networks using images from lung cancer cell lines. Methods: We performed transfer learning of convolutional neural networks. Initially, the models were pre-trained using images obtained from lung cancer cell lines. The model’s accuracy was improved by training with a limited number of clinical CTC images. Results: Transfer learning significantly improved the CTC classification accuracy to an average of 99.51%, compared to 96.96% for a model trained solely on pre-trained cell lines (p < 0.05). This approach showed notable efficacy when clinical training images were limited, achieving statistically significant accuracy improvements with as few as 17 clinical CTC images (p < 0.05). Conclusions: Overall, our findings demonstrate that pre-training with cancer cell lines enables rapid and highly accurate automated CTC recognition even with limited clinical data, significantly enhancing clinical applicability and potential utility across diverse cancer diagnostic workflows. |
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AbstractList | Background/Objectives: Circulating tumor cells (CTCs) are important biomarkers for predicting prognosis and evaluating treatment efficacy in cancer. We developed the “CTC-Chip” system based on microfluidics, enabling highly sensitive CTC detection and prognostic assessment in lung cancer and malignant pleural mesothelioma. However, the final identification and enumeration of CTCs require manual intervention, which is time-consuming, prone to human error, and necessitates the involvement of experienced medical professionals. Medical image recognition using machine learning can reduce workload and improve automation. However, CTCs are rare in clinical samples, limiting the training data available to construct a robust CTC image recognition system. In this study, we established a highly accurate artificial intelligence-based CTC recognition system by pre-training convolutional neural networks using images from lung cancer cell lines. Methods: We performed transfer learning of convolutional neural networks. Initially, the models were pre-trained using images obtained from lung cancer cell lines. The model’s accuracy was improved by training with a limited number of clinical CTC images. Results: Transfer learning significantly improved the CTC classification accuracy to an average of 99.51%, compared to 96.96% for a model trained solely on pre-trained cell lines (p < 0.05). This approach showed notable efficacy when clinical training images were limited, achieving statistically significant accuracy improvements with as few as 17 clinical CTC images (p < 0.05). Conclusions: Overall, our findings demonstrate that pre-training with cancer cell lines enables rapid and highly accurate automated CTC recognition even with limited clinical data, significantly enhancing clinical applicability and potential utility across diverse cancer diagnostic workflows. Circulating tumor cells (CTCs) are rare cancer cells in the blood that can help predict treatment outcomes. However, identifying them manually is slow and needs expertise. In this study, we developed an AI system that accurately detects CTCs using image recognition. To solve the problem of limited clinical images, we first trained the AI system with lung cancer cell line images and then applied transfer learning using a small number of real CTC images. This approach significantly improved accuracy, even with only 17 clinical images. The final model reached 99.5% accuracy. This method reduces the need for large clinical datasets and supports faster, more reliable CTC detection in lung cancer. It may also be applicable to other cancer types and diagnostic workflows. Background/Objectives: Circulating tumor cells (CTCs) are important biomarkers for predicting prognosis and evaluating treatment efficacy in cancer. We developed the “CTC-Chip” system based on microfluidics, enabling highly sensitive CTC detection and prognostic assessment in lung cancer and malignant pleural mesothelioma. However, the final identification and enumeration of CTCs require manual intervention, which is time-consuming, prone to human error, and necessitates the involvement of experienced medical professionals. Medical image recognition using machine learning can reduce workload and improve automation. However, CTCs are rare in clinical samples, limiting the training data available to construct a robust CTC image recognition system. In this study, we established a highly accurate artificial intelligence-based CTC recognition system by pre-training convolutional neural networks using images from lung cancer cell lines. Methods: We performed transfer learning of convolutional neural networks. Initially, the models were pre-trained using images obtained from lung cancer cell lines. The model’s accuracy was improved by training with a limited number of clinical CTC images. Results: Transfer learning significantly improved the CTC classification accuracy to an average of 99.51%, compared to 96.96% for a model trained solely on pre-trained cell lines ( p < 0.05). This approach showed notable efficacy when clinical training images were limited, achieving statistically significant accuracy improvements with as few as 17 clinical CTC images ( p < 0.05). Conclusions: Overall, our findings demonstrate that pre-training with cancer cell lines enables rapid and highly accurate automated CTC recognition even with limited clinical data, significantly enhancing clinical applicability and potential utility across diverse cancer diagnostic workflows. Circulating tumor cells (CTCs) are rare cancer cells in the blood that can help predict treatment outcomes. However, identifying them manually is slow and needs expertise. In this study, we developed an AI system that accurately detects CTCs using image recognition. To solve the problem of limited clinical images, we first trained the AI system with lung cancer cell line images and then applied transfer learning using a small number of real CTC images. This approach significantly improved accuracy, even with only 17 clinical images. The final model reached 99.5% accuracy. This method reduces the need for large clinical datasets and supports faster, more reliable CTC detection in lung cancer. It may also be applicable to other cancer types and diagnostic workflows. Circulating tumor cells (CTCs) are important biomarkers for predicting prognosis and evaluating treatment efficacy in cancer. We developed the "CTC-Chip" system based on microfluidics, enabling highly sensitive CTC detection and prognostic assessment in lung cancer and malignant pleural mesothelioma. However, the final identification and enumeration of CTCs require manual intervention, which is time-consuming, prone to human error, and necessitates the involvement of experienced medical professionals. Medical image recognition using machine learning can reduce workload and improve automation. However, CTCs are rare in clinical samples, limiting the training data available to construct a robust CTC image recognition system. In this study, we established a highly accurate artificial intelligence-based CTC recognition system by pre-training convolutional neural networks using images from lung cancer cell lines. We performed transfer learning of convolutional neural networks. Initially, the models were pre-trained using images obtained from lung cancer cell lines. The model's accuracy was improved by training with a limited number of clinical CTC images. Transfer learning significantly improved the CTC classification accuracy to an average of 99.51%, compared to 96.96% for a model trained solely on pre-trained cell lines ( < 0.05). This approach showed notable efficacy when clinical training images were limited, achieving statistically significant accuracy improvements with as few as 17 clinical CTC images ( < 0.05). Overall, our findings demonstrate that pre-training with cancer cell lines enables rapid and highly accurate automated CTC recognition even with limited clinical data, significantly enhancing clinical applicability and potential utility across diverse cancer diagnostic workflows. Circulating tumor cells (CTCs) are important biomarkers for predicting prognosis and evaluating treatment efficacy in cancer. We developed the "CTC-Chip" system based on microfluidics, enabling highly sensitive CTC detection and prognostic assessment in lung cancer and malignant pleural mesothelioma. However, the final identification and enumeration of CTCs require manual intervention, which is time-consuming, prone to human error, and necessitates the involvement of experienced medical professionals. Medical image recognition using machine learning can reduce workload and improve automation. However, CTCs are rare in clinical samples, limiting the training data available to construct a robust CTC image recognition system. In this study, we established a highly accurate artificial intelligence-based CTC recognition system by pre-training convolutional neural networks using images from lung cancer cell lines.BACKGROUND/OBJECTIVESCirculating tumor cells (CTCs) are important biomarkers for predicting prognosis and evaluating treatment efficacy in cancer. We developed the "CTC-Chip" system based on microfluidics, enabling highly sensitive CTC detection and prognostic assessment in lung cancer and malignant pleural mesothelioma. However, the final identification and enumeration of CTCs require manual intervention, which is time-consuming, prone to human error, and necessitates the involvement of experienced medical professionals. Medical image recognition using machine learning can reduce workload and improve automation. However, CTCs are rare in clinical samples, limiting the training data available to construct a robust CTC image recognition system. In this study, we established a highly accurate artificial intelligence-based CTC recognition system by pre-training convolutional neural networks using images from lung cancer cell lines.We performed transfer learning of convolutional neural networks. Initially, the models were pre-trained using images obtained from lung cancer cell lines. The model's accuracy was improved by training with a limited number of clinical CTC images.METHODSWe performed transfer learning of convolutional neural networks. Initially, the models were pre-trained using images obtained from lung cancer cell lines. The model's accuracy was improved by training with a limited number of clinical CTC images.Transfer learning significantly improved the CTC classification accuracy to an average of 99.51%, compared to 96.96% for a model trained solely on pre-trained cell lines (p < 0.05). This approach showed notable efficacy when clinical training images were limited, achieving statistically significant accuracy improvements with as few as 17 clinical CTC images (p < 0.05).RESULTSTransfer learning significantly improved the CTC classification accuracy to an average of 99.51%, compared to 96.96% for a model trained solely on pre-trained cell lines (p < 0.05). This approach showed notable efficacy when clinical training images were limited, achieving statistically significant accuracy improvements with as few as 17 clinical CTC images (p < 0.05).Overall, our findings demonstrate that pre-training with cancer cell lines enables rapid and highly accurate automated CTC recognition even with limited clinical data, significantly enhancing clinical applicability and potential utility across diverse cancer diagnostic workflows.CONCLUSIONSOverall, our findings demonstrate that pre-training with cancer cell lines enables rapid and highly accurate automated CTC recognition even with limited clinical data, significantly enhancing clinical applicability and potential utility across diverse cancer diagnostic workflows. |
Audience | Academic |
Author | Matsumiya, Hiroki Yoshino, Yuki Kuwata, Taiji Nemoto, Yukiko Kuroda, Koji Kishi, Yusuke Kanayama, Masatoshi Takenaka, Masaru Yoneda, Kazue Mori, Masataka Sasaki, Tohru Terabayashi, Kenji Ohnaga, Takashi Tanaka, Fumihiro Oyama, Rintaro Nishizawa, Natsumasa Honda, Yohei Chikaishi, Yasuhiro |
AuthorAffiliation | 1 Second Department of Surgery, School of Medicine, University of Occupational and Environmental Health, Kitakyushu 807-8555, Japan; masataka-m@med.uoeh-u.ac.jp (M.M.); masatoshi-kanayama@med.uoeh-u.ac.jp (M.K.); rintarooyama@med.uoeh-u.ac.jp (R.O.); yukikofukuichi@med.uoeh-u.ac.jp (Y.N.); nmasamed@med.uoeh-u.ac.jp (N.N.); yoheihonda@med.uoeh-u.ac.jp (Y.H.); t-kuwata@med.uoeh-u.ac.jp (T.K.); m-takenaka@med.uoeh-u.ac.jp (M.T.); cywmd0k2@med.uoeh-u.ac.jp (Y.C.); yoneda@med.uoeh-u.ac.jp (K.Y.); kuroda-k@med.uoeh-u.ac.jp (K.K.); ohnaga@pe.ctt.ne.jp (T.O.); ftanaka@med.uoeh-u.ac.jp (F.T.) 2 Department of Mechanical and Intellectual Systems Engineering, Faculty of Engineering, University of Toyama, Toyama 930-8555, Japan; tera@eng.u-toyama.ac.jp (K.T.); yusuke.kishi1@konicaminolta.com (Y.K.); y.yoshino@shimz.co.jp (Y.Y.); tsasaki@eng.u-toyama.ac.jp (T.S.) |
AuthorAffiliation_xml | – name: 2 Department of Mechanical and Intellectual Systems Engineering, Faculty of Engineering, University of Toyama, Toyama 930-8555, Japan; tera@eng.u-toyama.ac.jp (K.T.); yusuke.kishi1@konicaminolta.com (Y.K.); y.yoshino@shimz.co.jp (Y.Y.); tsasaki@eng.u-toyama.ac.jp (T.S.) – name: 1 Second Department of Surgery, School of Medicine, University of Occupational and Environmental Health, Kitakyushu 807-8555, Japan; masataka-m@med.uoeh-u.ac.jp (M.M.); masatoshi-kanayama@med.uoeh-u.ac.jp (M.K.); rintarooyama@med.uoeh-u.ac.jp (R.O.); yukikofukuichi@med.uoeh-u.ac.jp (Y.N.); nmasamed@med.uoeh-u.ac.jp (N.N.); yoheihonda@med.uoeh-u.ac.jp (Y.H.); t-kuwata@med.uoeh-u.ac.jp (T.K.); m-takenaka@med.uoeh-u.ac.jp (M.T.); cywmd0k2@med.uoeh-u.ac.jp (Y.C.); yoneda@med.uoeh-u.ac.jp (K.Y.); kuroda-k@med.uoeh-u.ac.jp (K.K.); ohnaga@pe.ctt.ne.jp (T.O.); ftanaka@med.uoeh-u.ac.jp (F.T.) |
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Cites_doi | 10.1016/j.media.2022.102444 10.1158/1078-0432.CCR-06-1695 10.1007/s12154-013-0094-5 10.1038/s41598-020-69056-1 10.21037/tlcr-22-712 10.1111/cas.15255 10.3389/fbioe.2020.00897 10.1109/ISM.2015.126 10.1038/s42256-020-0153-x 10.3892/ol.2023.13906 10.1007/s10544-013-9775-7 10.1186/s13073-020-00728-3 10.3390/ijms21041475 10.1038/nrc3820 10.1158/1078-0432.CCR-09-1095 10.1016/j.ymeth.2010.01.027 10.1186/s40537-023-00727-2 10.3892/or.2016.5235 10.1038/nature14539 10.1186/s12943-021-01392-w 10.1530/ERC-21-0179 10.3389/fonc.2021.686365 10.1002/cyto.a.22993 10.1158/1078-0432.CCR-04-0378 10.3389/fonc.2021.734959 10.1117/1.JBO.30.S1.S13709 10.3389/fonc.2024.1411731 10.1158/0008-5472.CAN-18-0653 10.1016/j.canlet.2006.12.014 10.1109/TSMC.1979.4310076 10.3389/fcell.2021.666156 10.2147/OTT.S249063 10.7150/thno.5195 |
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Keywords | lung cancer tumor cell transfer learning cell lines artificial intelligence |
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References | Toratani (ref_19) 2018; 78 Xu (ref_2) 2021; 20 Otsu (ref_29) 1979; 9 ref_33 Akashi (ref_28) 2023; 26 Aceto (ref_1) 2020; 12 ref_30 Childs (ref_6) 2021; 28 ref_17 Benali (ref_25) 2007; 253 Allard (ref_10) 2004; 10 Lannin (ref_18) 2016; 89 Alzubaidi (ref_32) 2023; 10 Kanayama (ref_15) 2022; 113 Chen (ref_22) 2022; 79 Chen (ref_5) 2020; 13 Sandri (ref_26) 2010; 50 Pantel (ref_27) 2014; 14 Chikaishi (ref_14) 2017; 37 Riethdort (ref_11) 2007; 13 ref_23 ref_21 LeCun (ref_31) 2015; 521 Ohnaga (ref_13) 2013; 15 Toseland (ref_16) 2013; 6 Hamilton (ref_3) 2023; 12 Zeune (ref_20) 2020; 2 Tanaka (ref_12) 2009; 15 Hong (ref_24) 2013; 3 ref_9 ref_8 ref_4 ref_7 |
References_xml | – volume: 79 start-page: 102444 year: 2022 ident: ref_22 article-title: Recent advances and clinical applications of deep learning in medical image analysis publication-title: Med. Image Anal. doi: 10.1016/j.media.2022.102444 – volume: 13 start-page: 920 year: 2007 ident: ref_11 article-title: Detection of circulating tumor cells in peripheral blood of patients with metastatic breast cancer: A validation study of the CellSearch System publication-title: Clin. Cancer Res. doi: 10.1158/1078-0432.CCR-06-1695 – volume: 6 start-page: 85 year: 2013 ident: ref_16 article-title: Fluorescent labeling and modification of proteins publication-title: J. Chem. Biol. doi: 10.1007/s12154-013-0094-5 – ident: ref_21 doi: 10.1038/s41598-020-69056-1 – volume: 12 start-page: 877 year: 2023 ident: ref_3 article-title: Significance of circulating tumor cells in lung cancer: A narrative review publication-title: Transl. Lung Cancer Res. doi: 10.21037/tlcr-22-712 – volume: 113 start-page: 1028 year: 2022 ident: ref_15 article-title: Prognostic impact of circulating tumor cells detected with the microfluidic “universal CTC-chip” for primary lung cancer publication-title: Cancer Sci. doi: 10.1111/cas.15255 – ident: ref_23 doi: 10.3389/fbioe.2020.00897 – ident: ref_30 doi: 10.1109/ISM.2015.126 – volume: 2 start-page: 124 year: 2020 ident: ref_20 article-title: Deep learning of circulating tumour cells publication-title: Nat. Mach. Intell. doi: 10.1038/s42256-020-0153-x – volume: 26 start-page: 320 year: 2023 ident: ref_28 article-title: The use of an artificial intelligence algorithm for circulating tumor cell detection in patients with esophageal cancer publication-title: Oncol. Lett. doi: 10.3892/ol.2023.13906 – volume: 15 start-page: 611 year: 2013 ident: ref_13 article-title: Polymeric microfluidic devices exhibiting sufficient capture of cancer cell line for isolation of circulating tumor cells publication-title: Biomed. Microdevices doi: 10.1007/s10544-013-9775-7 – volume: 12 start-page: 31 year: 2020 ident: ref_1 article-title: Tracking cancer progression: From circulating tumor cells to metastasis publication-title: Genome Med. doi: 10.1186/s13073-020-00728-3 – ident: ref_9 doi: 10.3390/ijms21041475 – volume: 14 start-page: 623 year: 2014 ident: ref_27 article-title: Challenges in circulating tumour cell research publication-title: Nat. Rev. Cancer doi: 10.1038/nrc3820 – volume: 15 start-page: 6980 year: 2009 ident: ref_12 article-title: Circulating tumor cell as a diagnostic marker in primary lung cancer publication-title: Clin. Cancer Res. doi: 10.1158/1078-0432.CCR-09-1095 – volume: 50 start-page: 289 year: 2010 ident: ref_26 article-title: Circulating tumour cells in clinical practice: Methods of detection and possible characterization publication-title: Methods doi: 10.1016/j.ymeth.2010.01.027 – volume: 10 start-page: 46 year: 2023 ident: ref_32 article-title: A survey on deep learning tools dealing with data scarcity: Definitions, challenges, solutions, tips, and applications publication-title: J. Big Data. doi: 10.1186/s40537-023-00727-2 – volume: 37 start-page: 77 year: 2017 ident: ref_14 article-title: EpCAM-independent capture of circulating tumor cells with a ‘universal CTC-chip’ publication-title: Oncol. Rep. doi: 10.3892/or.2016.5235 – volume: 521 start-page: 436 year: 2015 ident: ref_31 article-title: Deep learning publication-title: Nature doi: 10.1038/nature14539 – volume: 20 start-page: 104 year: 2021 ident: ref_2 article-title: Using single-cell sequencing technology to detect circulating tumor cells in solid tumors publication-title: Mol. Cancer doi: 10.1186/s12943-021-01392-w – volume: 28 start-page: 631 year: 2021 ident: ref_6 article-title: Whole-genome sequencing of single circulating tumor cells from neuroendocrine neoplasms publication-title: Endocr. Relat. Cancer doi: 10.1530/ERC-21-0179 – ident: ref_7 doi: 10.3389/fonc.2021.686365 – volume: 89 start-page: 922 year: 2016 ident: ref_18 article-title: Comparison and optimization of machine learning methods for automated classification of circulating tumor cells publication-title: Cytom. A. doi: 10.1002/cyto.a.22993 – volume: 10 start-page: 6897 year: 2004 ident: ref_10 article-title: Tumor cells circulate in the peripheral blood of all major carcinomas but not in healthy subjects or patients with nonmalignant diseases publication-title: Clin. Cancer Res. doi: 10.1158/1078-0432.CCR-04-0378 – ident: ref_33 doi: 10.3389/fonc.2021.734959 – ident: ref_17 doi: 10.1117/1.JBO.30.S1.S13709 – ident: ref_4 doi: 10.3389/fonc.2024.1411731 – volume: 78 start-page: 6703 year: 2018 ident: ref_19 article-title: A convolutional neural network uses microscopic images to differentiate between mouse and human cell lines and their radioresistant clones publication-title: Cancer Res. doi: 10.1158/0008-5472.CAN-18-0653 – volume: 253 start-page: 180 year: 2007 ident: ref_25 article-title: Circulating tumor cells (CTC) detection: Clinical impact and future directions publication-title: Cancer Lett. doi: 10.1016/j.canlet.2006.12.014 – volume: 9 start-page: 62 year: 1979 ident: ref_29 article-title: A threshold selection method from gray-level histograms publication-title: IEEE Trans. Syst. Man Cybern. doi: 10.1109/TSMC.1979.4310076 – ident: ref_8 doi: 10.3389/fcell.2021.666156 – volume: 13 start-page: 4943 year: 2020 ident: ref_5 article-title: HMGA1 regulates the stem cell-like properties of circulating tumor cells from GIST patients via Wnt/β-catenin pathway publication-title: Onco Targets Ther. doi: 10.2147/OTT.S249063 – volume: 3 start-page: 377 year: 2013 ident: ref_24 article-title: Detecting circulating tumor cells: Current challenges and new trends publication-title: Theranostics doi: 10.7150/thno.5195 |
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Snippet | Background/Objectives: Circulating tumor cells (CTCs) are important biomarkers for predicting prognosis and evaluating treatment efficacy in cancer. We... Circulating tumor cells (CTCs) are important biomarkers for predicting prognosis and evaluating treatment efficacy in cancer. We developed the "CTC-Chip"... Circulating tumor cells (CTCs) are rare cancer cells in the blood that can help predict treatment outcomes. However, identifying them manually is slow and... |
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SubjectTerms | Accuracy Algorithms Antibodies Artificial intelligence Automation Care and treatment Cells Classification Datasets Deep learning Development and progression Diagnosis Enumeration Health aspects Lung cancer Machine learning Medical imaging Medical personnel Medical research Mesothelioma Metastasis Microfluidics Mutation Neural networks Risk factors Software Statistical analysis Testing Training Transfer learning Tumor cell lines Tumor cells Tumors Viral antibodies |
Title | Establishing a Highly Accurate Circulating Tumor Cell Image Recognition System for Human Lung Cancer by Pre-Training on Lung Cancer Cell Lines |
URI | https://www.ncbi.nlm.nih.gov/pubmed/40723173 https://www.proquest.com/docview/3233103934 https://www.proquest.com/docview/3234312458 https://pubmed.ncbi.nlm.nih.gov/PMC12293340 |
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