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Article

Decoding Lung Cancer Radiogenomics: A Custom Clustering/Classification Methodology to Simultaneously Identify Important Imaging Features and Relevant Genes

1
School of Engineering and Applied Science, George Washington University, Washington, DC 20052, USA
2
Department of Radiology, School of Medicine and Health Sciences, George Washington University, Washington, DC 20052, USA
3
Department of Radiation Oncology, School of Medicine and Health Sciences, George Washington University, Washington, DC 20052, USA
*
Author to whom correspondence should be addressed.
Appl. Sci. 2025, 15(7), 4053; https://doi.org/10.3390/app15074053
Submission received: 26 February 2025 / Revised: 27 March 2025 / Accepted: 2 April 2025 / Published: 7 April 2025

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This paper presents a custom combined clustering-image classification methodology to group genetic mutation patterns representative of lung cancer using CT data. This methodology could be applied to other radiogenomic or image classification problems with partial or completely unlabeled images to cluster final results.

Abstract

Background: This study evaluated a custom algorithm that sought to perform a radiogenomic analysis on lung cancer genetic and imaging data, specifically by using machine learning to see whether a custom clustering/classification method could simultaneously identify features from imaging data that correspond to genetic markers. Methods: CT imaging data and genetic mutation data for 281 subjects with NSCLC were collected from the CPTAC-LUAD and TCGA-LUSC databases on TCIA. The algorithm was run as follows: (1) genetic clusters were initialized using random clusters, binary matrix factorization, or k-means; (2) image classification was run on CT data for these genetic clusters; (3) misclassified subjects were re-classified based on the image classification algorithm; and (4) the algorithm was run until an accuracy of 90% or no improvement after 10 runs. Input genetic mutations were evaluated for potential medical treatments and severity to provide clinical relevance. Results: The image classification algorithm was able to achieve a >90% accuracy after nine algorithm runs and grouped subjects from a starting five clusters to four final clusters, where final image classification accuracy was better than every initial clustered accuracy. These clusters were stable across all three test runs. A total of thirty-eight genes from the top hundred across each subject were identified with specific severity or treatment data; twelve of these genes are listed. Conclusion: This small pilot study presented a potential way to identify genetic patterns from image data and presented a methodology that could group images with no labels or only partial labels for future problems.
Keywords: lung cancer; machine learning; radiogenomics; deep clustering; deep learning; ResNet lung cancer; machine learning; radiogenomics; deep clustering; deep learning; ResNet

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MDPI and ACS Style

Provenzano, D.; Lichtenberger, J.P.; Goyal, S.; Rao, Y.J. Decoding Lung Cancer Radiogenomics: A Custom Clustering/Classification Methodology to Simultaneously Identify Important Imaging Features and Relevant Genes. Appl. Sci. 2025, 15, 4053. https://doi.org/10.3390/app15074053

AMA Style

Provenzano D, Lichtenberger JP, Goyal S, Rao YJ. Decoding Lung Cancer Radiogenomics: A Custom Clustering/Classification Methodology to Simultaneously Identify Important Imaging Features and Relevant Genes. Applied Sciences. 2025; 15(7):4053. https://doi.org/10.3390/app15074053

Chicago/Turabian Style

Provenzano, Destie, John P. Lichtenberger, Sharad Goyal, and Yuan James Rao. 2025. "Decoding Lung Cancer Radiogenomics: A Custom Clustering/Classification Methodology to Simultaneously Identify Important Imaging Features and Relevant Genes" Applied Sciences 15, no. 7: 4053. https://doi.org/10.3390/app15074053

APA Style

Provenzano, D., Lichtenberger, J. P., Goyal, S., & Rao, Y. J. (2025). Decoding Lung Cancer Radiogenomics: A Custom Clustering/Classification Methodology to Simultaneously Identify Important Imaging Features and Relevant Genes. Applied Sciences, 15(7), 4053. https://doi.org/10.3390/app15074053

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