Evidence map›Paper›PMID 40596917›Full record

ArticleBMC medical imaging2025

Enhancing radiomics robustness using bayesian penalized likelihood PET reconstruction: application to Phantom and non-small cell lung cancer patient studies.

Zahra Valibeiglou, Jalil Pirayesh Islamian, Yunus Soleymani, Saeed Farzanehfar, Farahnaz Aghahosseini, Neda Gilani, Arman Rahmim, Peyman Sheikhzadeh

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Article in BMC medical imaging, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

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8 authors.

Zahra ValibeiglouDepartment of Medical Physics, School of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran.
Jalil Pirayesh IslamianDepartment of Medical Physics, School of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran. pirayeshj@tbzmed.ac.ir.
Yunus SoleymaniDepartment of Neuroscience and Addiction Studies, School of Advanced Technologies in Medicine, Tehran University of Medical Sciences, Tehran, Iran.
Saeed FarzanehfarDepartment of Nuclear Medicine, Faculty of Medicine, IKHC, Tehran University of Medical Sciences, Tehran, Iran.
Farahnaz AghahosseiniDepartment of Nuclear Medicine, Faculty of Medicine, IKHC, Tehran University of Medical Sciences, Tehran, Iran.
Neda GilaniDepartment of Statistics and Epidemiology, Faculty of Health, Tabriz University of Medical Sciences, Tabriz, Iran.
Arman RahmimDepartment of Integrative Oncology, BC Cancer Research Institute, Vancouver, BC, Canada.
Peyman SheikhzadehDepartment of Nuclear Medicine, Faculty of Medicine, IKHC, Tehran University of Medical Sciences, Tehran, Iran. psh82@yahoo.com.ORCID http://orcid.org/0000-0003-3053-2641

Funding

Tabriz University of Medical Sciences 71082
6 · The paper itself

Abstract

purposeThis study aims to enhance the diagnostic and prognostic capabilities of PET imaging through improved robustness of radiomics features, utilizing the Bayesian penalized likelihood (BPL) reconstruction algorithm. Specifically, we focus on

methodWe studied a NEMA image quality (IQ) phantom and 15 patient PET lesions (14 NSCLC patients selected from 30 patients originally considered). The study assessed the stability of radiomics features against various imaging parameters, emphasizing the impact of the BPL reconstruction algorithm with varying β-values (50, 100, 150, 200, 250, 300, 350, 400, 450, 500, 600, and 700) and three phantom lesion to background ratios (LBRs) of 2:1, 4:1, and 8:1. Manual segmentation was performed, and subsequently, 130 radiomic features were extracted from the reconstructed images. The stability of radiomics features was assessed by calculating the coefficient of variation (COV) for each feature across variations in reconstruction parameters. A COV of ≤ 5% indicated high stability.

resultsOur results indicate that morphological and intensity-based features exhibit excellent stability, with a COV of less than 5%. Texture-based features, despite their complexity, also demonstrated robustness. Specifically, 32.3%, 39.2%, 42.3%, and 37.6% of features exhibited high stability in phantom LBR 2:1, phantom LBR 4:1, phantom LBR 8:1, and patient studies, respectively. Overall, 13 morphological, 8 intensity, 6 intensity-histogram, and 5 texture-based features were found to be highly stable against different LBRs and reconstruction parameters.

conclusionsThe BPL reconstruction algorithm may enhance the robustness of PET radiomics features, supporting their use in clinical settings for non-invasive diagnosis and staging. The adoption of BPL towards improved PET radiomics robustness has the potential to transform NSCLC evaluation and management, but still needs standardization.

Indexed as

Carcinoma, Non-Small-Cell LungImage Processing, Computer-AssistedLung NeoplasmsPositron-Emission TomographyAgedAlgorithmsBayes TheoremFemaleFluorodeoxyglucose F18HumansMaleMiddle AgedPhantoms, ImagingRadiomicsRadiopharmaceuticalsFluorodeoxyglucose F18Radiopharmaceuticals18F-FDG PETNEMA image quality phantomNon-small cell lung carcinomaRadiomics featuresReconstruction algorithm

Identifiers

PMID40596917
PMCPMC12210655

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