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Relationship of FDG PET/CT Textural Features with the Tumor Microenvironment and Recurrence Risks in Patients with Advanced Gastric Cancers

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Abstract
The relationship between 2-deoxy-2-[(18)F]fluoro-D-glucose (FDG) positron emission tomography/computed tomography (PET/CT) textural features and histopathological findings in gastric cancer has not been fully evaluated. We investigated the relationship between the textural features of primary tumors on FDG PET/CT with histopathological findings and recurrence-free survival (RFS) in patients with advanced gastric cancer (AGC). Fifty-six patients with AGC who underwent FDG PET/CT for staging work-ups were retrospectively enrolled. Conventional parameters and the first- and second-order textural features of AGC were extracted using PET textural analysis. Upon histopathological analysis, along with histopathological classification and staging, the degree of CD4, CD8, and CD163 cell infiltrations and expressions of interleukin-6 and matrix-metalloproteinase-11 (MMP-11) in the primary tumor were assessed. The histopathological classification, Lauren classification, lymph node metastasis, CD8 T lymphocyte and CD163 macrophage infiltrations, and MMP-11 expression were significantly associated with the textural features of AGC. The multivariate survival analysis showed that increased FDG uptake and intra-tumoral metabolic heterogeneity were significantly associated with an increased risk of recurrence after curative surgery. Textural features of AGC on FDG PET/CT showed significant correlations with the inflammatory response in the tumor microenvironment and histopathological features of AGC, and they showed significant prognostic values for predicting RFS.
All Author(s)
H. Ahn ; G. J. Song ; S. H. Jang ; H. J. Lee ; M. S. Lee ; J. H. Lee ; M. H. Oh ; G. C. Jeong ; S. M. Lee ; J. W. Lee
Issued Date
2022
Type
Article
Keyword
F-18 fluorodeoxyglucosepositron emission tomographyprognosistextural feature
Publisher
Irish Association for Cancer Research
Spanish Association for Cancer Research
Biomedical Research Centre
British Neuro-Oncology Society
Spanish Group for Cancer Immuno-Biotherapy
ISSN
2072-6694
Citation Title
Cancers
Citation Volume
14
Citation Number
16
Citation Start Page
3936
Citation End Page
3936
Language(ISO)
eng
DOI
10.3390/cancers14163936
URI
http://schca-ir.schmc.ac.kr/handle/2022.oak/1729
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