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Association between PD-L1 expression and 18F-FDG uptake in ovarian cancer
Objective Immunotherapy for programmed cell death 1 (PD-1) and its ligand, PD-L1, has been considered an effective treatment for ovarian cancer. 18 F-labeled fluoro-2-deoxyglucose positron emission tomography/computed tomography ( 18 F-FDG PET/CT) is a widely used noninvasive imaging tool for diagno...
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Published in: | Annals of nuclear medicine 2021-04, Vol.35 (4), p.415-420 |
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Main Authors: | , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Objective
Immunotherapy for programmed cell death 1 (PD-1) and its ligand, PD-L1, has been considered an effective treatment for ovarian cancer.
18
F-labeled fluoro-2-deoxyglucose positron emission tomography/computed tomography (
18
F-FDG PET/CT) is a widely used noninvasive imaging tool for diagnosing several cancers. In this study, we investigated the association between PD-L1 expression and the maximum standardized uptake value (SUVmax) using
18
F-FDG PET/CT.
Methods
We retrospectively analyzed clinical data of patients with ovarian cancer who underwent
18
F-FDG PET/CT. Patients were categorized into two groups according to PD-L1 expression results. The relationship between clinicopathological characteristics of patients with ovarian cancer and PD-L1 expression was examined.
Results
SUVmax was significantly higher in PD-L1-positive tumors than in PD-L1-negative tumors (16.1 ± 5.2 and 12.7 ± 7.0, respectively;
p
= 0.026). There were no significant differences in age, histologic type, and tumor grade between the PD-L1-negative and PD-L1-positive groups. The receiver operating characteristic curve analysis demonstrated that the highest accuracy (61.8%) for predicting PD-L1 expression was obtained with an SUVmax cutoff value of 10.5.
Conclusion
There was a significant correlation between
18
F-FDG uptake and PD-L1 expression, suggesting a role of
18
F-FDG PET/CT in selecting ovarian cancer candidates for anti-PD-L1 antibody therapy. |
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ISSN: | 0914-7187 1864-6433 |
DOI: | 10.1007/s12149-020-01571-7 |