A Pilot Study on Quantitative Accuracy and Radiomic Feature Stability of Deep Progressive Learning Reconstruction in NSCLC PET.

A Pilot Study on Quantitative Accuracy and Radiomic Feature Stability of Deep Progressive Learning Reconstruction in NSCLC PET.

Publication date: Sep 02, 2025

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 (COV) 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 COV ≤ 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.

Concepts Keywords
Algorithmic Non-small-cell lung cancer
Cov10 Ordered-subset expectation maximization
Pilot Radiomics
Suv Standardized uptake value
Tumors

Semantics

Type Source Name
drug DRUGBANK D-Proline
disease IDO algorithm
disease MESH non-small cell lung cancer
pathway KEGG Non-small cell lung cancer
disease MESH tumors
disease IDO quality
disease IDO cell
disease MESH lung cancer

Original Article

(Visited 10 times, 1 visits today)

Leave a Comment

Your email address will not be published. Required fields are marked *