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KMID : 1148920140480040278
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Nuclear Medicine and Molecular Imaging
2014 Volume.48 No. 4 p.278 ~ p.286
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Autoclustering of Non-small Cell Lung Carcinoma Subtypes on 18F-FDG PET Using Texture Analysis: A Preliminary Result
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Ha Seung-Gyun
Choi Hong-Yoon
Cheon Gi-Jeong
Kang Keon-Wook
Chung June-Key
Kim Eui-Shin Edmund
Lee Dong-Soo
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Abstract
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Purpose: Texture analysis on 18F-fluorodeoxyglucose positron emission tomography (18F-FDG PET) scan is a relatively new imaging analysis tool to evaluate metabolic heterogeneity. We analyzed the difference in textural characteristics between non-small cell lung carcinoma (NSCLC) subtypes, namely adenocarcinoma (ADC) and squamous cell carcinoma (SqCC).
Methods: Diagnostic 18F-FDG PET/computed tomography (CT) scans of 30y patients (median age, 67; range, 42-88) with NSCLC (17 ADC and 13 SqCC) were retrospectively analyzed. Regions of interest were manually determined on selected transverse image containing the highest SUV value in tumors. Texture parameters were extracted by histogram-based algorithms, absolute gradient-based algorithms, run-length matrix-based algorithms, co-occurrence matrix-based algorithms, and autoregressive model-based algorithms. Twenty-four out of hundreds of texture features were selected by three algorithms: Fisher coefficient, minimization of both classification error probability and average correlation, and mutual information. Automated clustering of tumors was based on the most discriminating feature calculated by linear discriminant analysis (LDA). Each tumor subtype was determined by histopathologic examination after biopsy and surgery.
Results: Fifteen texture features had significant different values between ADC and SqCC. LDA with 24 automate-selected texture features accurately clustered between ADC and SqCC with 0.90 linear separability. There was no high correlation between SUVmax and texture parameters (|r|?≤?0.62).
Conclusion: Each subtype of NSCLC tumor has different metabolic heterogeneity. The results of this study support the potential of textural parameters on FDG PET as an imaging biomarker.
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KEYWORD
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Positron emission tomography, F-18 Fluorodeoxyglucose, Carcinoma, Non-small cell lung, Texture analysis, Cluster analysis
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