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Low-count 18F-FDG PET/CT using a deep-learning reconstruction algorithm on a 35-cm axial field-of-view digital PET system: a prospective clinical evaluation

Year: 2026
Type: article
Abstract: Background/Introduction: To determine how far injected activity can be reduced in clinical 18 F-FDG PET/CT while preserving clinical interpretability using a deep progressive reconstruction (DPR) algorithm on one of Europe’s first 35-cm axial field-of-view (AFOV) digital PET/CT systems. Methods: One hundred fifty consecutive patients undergoing vertex-to-mid-thigh 18 F-FDG PET/CT were prospectively included. All acquisitions were performed at 3 MBq/kg with an acquisition time of 120 s/bed. List-mode data were retrospectively truncated to simulate shorter acquisition durations of 90, 60, and 30 s/bed (corresponding to 75%, 50%, and 25% of the total counts, respectively). Images were reconstructed using EARL-2–compliant TOF-OSEM and DPR. Two blinded physicians scored image quality on a 5-point Likert scale; clinical interpretability was defined as a Likert score ≥ 3 . SUV peak , SUV max , signal-to-noise ratio (SNR), and lesion contrast-to-noise ratio (CNR) were measured using propagated volumes of interest. Results: DPR yielded higher qualitative image quality than EARL-2 OSEM at all count levels. At 60 s/bed ( ∼ 50% counts), DPR remained clinically interpretable, whereas matched-count EARL-2 OSEM showed marked image degradation. Lesion CNR was higher with DPR across all simulated count levels. SUV peak was largely preserved in reference tissues and increased modestly in lesions, whereas SUV max showed larger reconstruction-dependent increases. Conclusion: This prospective clinical evaluation demonstrates that, on a 35-cm AFOV digital PET/CT system, DPR enables an approximately 50% reduction in effective count statistics (60 s/bed or 1.5 MBq/kg under linear scaling assumptions) without compromising clinical interpretability. Quantitative SUV measurements, particularly SUV max , remain reconstruction dependent.
Language: English
Field: Medicine
Open Access status: hybrid
OpenAlex ID: W7167469297
FWCI:
Cites: 19
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Related to: 10