TY - JOUR
T1 - A Pilot Study on Quantitative Accuracy and Radiomic Feature Stability of Deep Progressive Learning Reconstruction in NSCLC PET
AU - Shiiba, Takuro
AU - Abe, Takeru
AU - Watanabe, Masanori
N1 - Publisher Copyright:
© The Author(s) under exclusive licence to Society for Imaging Informatics in Medicine 2025.
PY - 2025
Y1 - 2025
N2 - Deep progressive learning reconstruction (DPR) is a novel deep learning-based algorithm for PET imaging, yet its impact on quantitative metrics and radiomic feature stability is not fully characterized. This preliminary study systematically evaluated DPR against conventional ordered-subset expectation maximization (OSEM) in non-small cell lung cancer (NSCLC) PET imaging. In this retrospective study of 24 NSCLC patients, PET data were reconstructed using OSEM and three DPR strength levels. We compared standardized uptake values (SUV), contrast-to-noise ratio (CNR), and background noise. As a secondary objective, the stability of 93 radiomic features was quantified using an intra-patient coefficient of variation (COVRF) across all four reconstruction methods. DPR significantly increased SUV, particularly in smaller tumors, but this came at the expense of image quality, with only the lowest DPR strength improving CNR. The stability analysis revealed a stark stratification of radiomic features. While 31 features (33.3%) were robust against algorithmic changes (median COVRF ≤ 10%), a larger group of 38 features (40.9%), including the commonly used glcm_Contrast, proved highly unstable. In conclusion, DPR presents a critical trade-off between enhanced SUV quantification and image quality, requiring careful parameter optimization. Furthermore, our findings demonstrate that the stability of radiomic features is highly algorithm-dependent. The reliable application of advanced reconstruction techniques like DPR in quantitative and radiomic pipelines is therefore contingent upon a rigorous, evidence-based selection of features verified to be robust.
AB - Deep progressive learning reconstruction (DPR) is a novel deep learning-based algorithm for PET imaging, yet its impact on quantitative metrics and radiomic feature stability is not fully characterized. This preliminary study systematically evaluated DPR against conventional ordered-subset expectation maximization (OSEM) in non-small cell lung cancer (NSCLC) PET imaging. In this retrospective study of 24 NSCLC patients, PET data were reconstructed using OSEM and three DPR strength levels. We compared standardized uptake values (SUV), contrast-to-noise ratio (CNR), and background noise. As a secondary objective, the stability of 93 radiomic features was quantified using an intra-patient coefficient of variation (COVRF) across all four reconstruction methods. DPR significantly increased SUV, particularly in smaller tumors, but this came at the expense of image quality, with only the lowest DPR strength improving CNR. The stability analysis revealed a stark stratification of radiomic features. While 31 features (33.3%) were robust against algorithmic changes (median COVRF ≤ 10%), a larger group of 38 features (40.9%), including the commonly used glcm_Contrast, proved highly unstable. In conclusion, DPR presents a critical trade-off between enhanced SUV quantification and image quality, requiring careful parameter optimization. Furthermore, our findings demonstrate that the stability of radiomic features is highly algorithm-dependent. The reliable application of advanced reconstruction techniques like DPR in quantitative and radiomic pipelines is therefore contingent upon a rigorous, evidence-based selection of features verified to be robust.
KW - Deep progressive learning reconstruction
KW - Non-small-cell lung cancer
KW - Ordered-subset expectation maximization
KW - Radiomics
KW - Standardized uptake value
UR - https://www.scopus.com/pages/publications/105015070301
UR - https://www.scopus.com/inward/citedby.url?scp=105015070301&partnerID=8YFLogxK
U2 - 10.1007/s10278-025-01654-9
DO - 10.1007/s10278-025-01654-9
M3 - Article
AN - SCOPUS:105015070301
SN - 0897-1889
JO - Journal of Imaging Informatics in Medicine
JF - Journal of Imaging Informatics in Medicine
ER -