Document Type : Original Article
Authors
1
Department of Nuclear Medicine, Imam Khomeini Hospital Complex, Tehran University of Medical Sciences, Tehran, Iran
2
Research Center for Nuclear Medicine, Tehran University of Medical Sciences, Tehran, Iran
3
Department of Neuroscience and Addiction Studies, School of Advanced Technologies in Medicine, Tehran University of Medical Sciences, Tehran, Iran
4
Department of Radiotherapy, Faculty of Medicine, Madani Hospital, Tabriz University of Medical Sciences, Tabriz, Iran
5
Department of Nuclear Medicine, Emsey Hospital, Istanbul, Turkey
6
Department of Medical Physics, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran
7
Department of Nuclear Medicine, Omid PET/CT Center, Tabriz, Iran
8
Medical Radiation Sciences Research Center, Tabriz University of Medical Sciences, Tabriz, Iran
9
Department of Radiology, Faculty of Allied Medical Sciences, Tabriz University of Medical Sciences, Tabriz, Iran
10.22034/irjnm.2026.130602.1772
Abstract
Introduction: The stability of quantitative PET radiomics features is an important consideration for reproducible radiomics analysis. This study investigated the stability of textural PET radiomics features across different SUVmax-based VOI segmentation.
Methods: PET/CT images from 24 patients with primary colon adenocarcinoma and 24 patients with hepatic metastases were retrospectively analyzed. Lesion VOIs were automatically generated using four SUVmax-based segmentation thresholds (10%, 20%, 30%, and 40%). A total of 32 textural features were extracted for each VOI. Feature stability was assessed using the intraclass correlation coefficient (ICC), with 95% confidence intervals.
Results: The stability of textural radiomics features varied across individual features and SUVmax-based segmentation thresholds. In the liver metastasis cohort, 28.1% of features demonstrated good to excellent stability, compared with 53.1% in the colon adenocarcinoma cohort. The feature with the highest stability was GLZLM_HGZE in the liver metastasis cohort (ICC = 0.923) and GLZLM_SZHGE in the colon adenocarcinoma cohort (ICC = 0.947). Several of the features with the highest ICC values belonged to the GLZLM and GLRLM families, whereas GLCM features generally showed lower stability, particularly in the liver metastasis cohort.
Conclusion: Textural PET radiomics features exhibit feature-dependent stability to changes in SUVmax-based VOI segmentation thresholds. The identification of features that remain stable across segmentation conditions may help improve the reproducibility of PET radiomics analyses. Differences in the observed stability patterns between colon adenocarcinoma and hepatic metastases should be interpreted cautiously because lesion size, uptake characteristics, lesion-to-background contrast, and partial-volume effects may also contribute to these differences.
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