PulseExploreJournal ClubDebatesTrendingResearchersJournals
Instagram
HomeExploreJournal ClubTrending
Synapse
⌘+K
Synapse
June 21, 2024Heliyon1 citationsOpen Access

FET PET provides adjunctive value to FDG PET in distinction of spinal cord tumors

View Full Paper
PLPenghao LiuJHJing HuangWDWanru Duan

Key Points

Key points are not available for this paper at this time.

Abstract

ObjectiveThis study aimed to compare the diagnostic efficacy of O-(2-18F-fluoroethyl)-L-tyrosine (18F-FET) PET and 2-deoxy-2-18Ffluoro-D-deoxyglucose (18F-FDG) PET for spinal cord lesions.Materials and MethodsPaired preoperative 18F-FDG PET/MRI and 18F-FET PET/MRI scans were conducted on patients with suspected spinal cord tumors. Clinical manifestations and PET performance, including SUVmean, SUVmax, TBRmean, TBRmax, metabolic tumor volume (MTV), and total lesion metabolism (TLM), and tumor volume, were compared using group analysis and receiver operating characteristic (ROC) curves.ResultsThirty-five patients were categorized into three groups based on their pathological diagnosis: high-grade tumors (HGTs, n=6), low-grade tumors (LGTs, n=19), and non-tumor diseases (NTDs, n=10). The background SUVmean of 18F-FET PET was significantly lower than that of 18F-FDG PET (p0.05). The mass SUVmean, SUVmax, MTV, and TLM values of both 18F-FDG PET and 18F-FET PET were statistically different between HGTs and LGTs (p0.05). Notably, 18F-FET PET provided valuable supporting diagnostic evidence in 1 case of mixed neuronal-glial tumor (MNGT) and 2 cases of intramedullary inflammatory lesions. Optimal cut-off values of all measured parameters for distinguishing tumors and NTDs were determined through ROC analysis.Conclusion18F-FET PET presented comparable diagnostic performance to 18F-FDG PET in differentiating HGTs, LGTs, and NTDs, but exhibited particular utility in MNGT and inflammatory lesions.

Ask AI
Helpful
Bookmark
Share
View Full Paper

Cite This Study

Liu et al. (2024) studied this question.

synapsesocial.com/papers/68e63d15b6db6435875cece2https://doi.org/10.1016/j.heliyon.2024.e33353
Ask AI
Helpful
Bookmark
Share
View Full Paper