Evidence map›Paper›PMID 40266997›Full record

ArticleJournal of applied clinical medical physics2025

Unsupervised non-small cell lung cancer tumor segmentation using cycled generative adversarial network with similarity-based discriminator.

Chengyijue Fang, Xiaoyang Li, Yidong Yang

Abstract read
In one paragraph

Article in Journal of applied clinical medical physics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Chengyijue FangDepartment of Engineering and Applied Physics, University of Science and Technology of China, Hefei, Anhui, China.
Xiaoyang LiDepartment of Radiation Oncology, the First Affiliated Hospital of USTC, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, Anhui, China.
Yidong YangDepartment of Engineering and Applied Physics, University of Science and Technology of China, Hefei, Anhui, China.

Funding

Fundamental Research Funds for the Central Universities KY2030000197Hefei Comprehensive National Science CenterMinistry of Science and Technology of China Key Research and Development Projects 2023YFC3504200
6 · The paper itself

Abstract

backgroundTumor segmentation is crucial for lung disease diagnosis and treatment. Most existing deep learning-based automatic segmentation methods rely on manually annotated data for network training. PURPOSE: This study aims to develop an unsupervised tumor segmentation network smic-GAN by using a similarity-driven generative adversarial network trained with cycle strategy. The proposed method does not rely on any manual annotations and thus reduce the training data preparation workload.

methodsA total of 609 CT scans of lung cancer patients are collected, of which 504 are used for training, 35 for validation, and 70 for testing. Smic-GAN is developed and trained to transform lung CT slices with tumors into synthetic images without tumors. Residual images are obtained by subtracting synthetic images from original CT slices. Thresholding, 3D median filtering, morphological erosion, and dilation operations are implemented to generate binary tumor masks from the residual images. Dice similarity, positive predictive value (PPV), sensitivity (SEN), 95% Hausdorff distance (HD95) and average surface distance (ASD) are used to evaluate the accuracy of tumor contouring.

resultsThe smic-GAN method achieved a performance comparable to two supervised methods UNet and Incre-MRRN, and outperformed unsupervised cycle-GAN. The Dice value for smic-GAN is significantly better than cycle-GAN (74.5%

conclusionThe proposed smic-GAN performs comparably to the existing supervised methods UNet and Incre-MRRN. It does not rely on any manual annotations and can reduce the workload of training data preparation. It can also provide a good start for manual annotation in the training of supervised networks.

Indexed as

Carcinoma, Non-Small-Cell LungImage Processing, Computer-AssistedLung NeoplasmsTomography, X-Ray ComputedUnsupervised Machine LearningAlgorithmsDeep LearningGenerative Adversarial NetworksHumansNeural Networks, Computerautomated tumor segmentationcycle‐GANlung cancerunsupervised approach

Identifiers

PMID40266997
PMCPMC12148803

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.