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Prognostic Significance of the Bone Marrow-to-Aorta Uptake Ratio on 2-Deoxy-2-[(18)F]fluoro-d-glucose Positron Emission Tomography/Computed Tomography in Patients with Cholangiocarcinoma

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Abstract
2-Deoxy-2-[18F]fluoro-d-glucose (FDG) uptake of the reticuloendothelial system on positron emission tomography/computed tomography (PET/CT) is known to be related to systemic inflammatory response to cancer cells in patients with diverse malignancies. This retrospective study aimed to investigate whether FDG uptake by the reticuloendothelial system had a prognostic value in predicting progression-free survival (PFS) and overall survival (OS) in 138 cholangiocarcinoma patients. Quantifying FDG uptake of the aorta, bone marrow (BM), liver, and spleen from staging FDG PET/CT images, we found significant correlations between the BM-to-aorta uptake ratio (BAR), spleen-to-aorta uptake ratio, and BM-to-liver uptake ratio with tumor stage and serum inflammatory markers. In the multivariate survival analysis, BAR was an independent predictor of PFS (p = 0.016; hazard ratio, 2.308) and OS (p = 0.030; hazard ratio, 2.645). Patients with stages III-IV of the disease and a high BAR exhibited low 1-year PFS (35.8%) and OS (60.2%) rates, while those with stages I-II of the disease and low BAR showed robust rates of 90.0% and 96.7%, respectively. BAR measured on staging FDG PET/CT might be a potential imaging biomarker offering insights into the systemic inflammatory response and predicting prognosis in cholangiocarcinoma. This study highlights BAR as a promising, independent predictor with potential for personalized prognostication and treatment strategies.
All Author(s)
Jeong Won Lee ; Ik Dong Yoo ; Sun-Pyo Hong ; Beodeul Kang ; Jung Sun Kim ; Yung Kil Kim ; Sang Ho Bae ; Su Jin Jang ; Sang Mi Lee
Issued Date
2024
Type
Article
Keyword
F-18 fluorodeoxyglucosebone marrowcholangiocarcinomapositron emission tomographyspleen
Publisher
MDPI
ISSN
2227-9059
Citation Title
Biomedicines
Citation Volume
12
Citation Number
5
Citation Start Page
944
Citation End Page
944
Language(ISO)
eng
DOI
10.3390/biomedicines12050944
URI
http://schca-ir.schmc.ac.kr/handle/2022.oak/3460
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