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PD-L1 in Lung Adenocarcinoma: Insights into the Role of (18)F-FDG PET/CT

PURPOSE: This study aimed to evaluate the role of (18)F-fluorodeoxyglucose ((18)F-FDG) positron emission tomography (PET)/computed tomography (CT) in expression of tumor programmed death ligand-1 (PD-L1) expression and prognostic significance of (18)F-FDG PET/CT at different PD-L1 status in patients...

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Autores principales: Cui, Yan, Li, Xuena, Du, Bulin, Diao, Yao, Li, Yaming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7394511/
https://www.ncbi.nlm.nih.gov/pubmed/32801879
http://dx.doi.org/10.2147/CMAR.S256871
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author Cui, Yan
Li, Xuena
Du, Bulin
Diao, Yao
Li, Yaming
author_facet Cui, Yan
Li, Xuena
Du, Bulin
Diao, Yao
Li, Yaming
author_sort Cui, Yan
collection PubMed
description PURPOSE: This study aimed to evaluate the role of (18)F-fluorodeoxyglucose ((18)F-FDG) positron emission tomography (PET)/computed tomography (CT) in expression of tumor programmed death ligand-1 (PD-L1) expression and prognostic significance of (18)F-FDG PET/CT at different PD-L1 status in patients with lung adenocarcinoma. PATIENTS AND METHODS: Seventy-three patients with primary lung adenocarcinoma who received (18)F-FDG PET/CT before treatment were retrospectively included in this study. Expression of tumor PD-L1, programmed death-1 (PD-1) and glucose metabolic parameters were evaluated. RESULTS: Tumor PD-L1 expression was positively correlated with maximum standardized uptake value (SUVmax), total lesion glycolysis (TLG), hexokinase II (HK-II) and glucose transporter 1 (GLUT-1) (P<0.0001 for all). SUVmax was a unique independent predictor of tumor PD-L1 expression, with an optimal cut-off value of 9.5. For all the patients, tumor stage (P<0.001) and SUVmax (P=0.009) were independent prognostic indicators of disease-free survival (DFS)/progression-free survival (PFS) while carcino-embryonic antigen (CEA) (P=0.003), Ki67 (P=0.042), PD-L1 (P=0.048) and TLG (P=0.004) were independent prognostic indicators of overall survival (OS). Tumor stage (P=0.004) and SUVmax (P=0.022) were independent prognostic indicators of DFS/PFS while TLG (P=0.012) and CEA (P=0.045) were independent prognostic indicators of OS in the PD-L1-positive group. In the PD-L1-negative group, tumor stage (P=0.002) and CEA (P=0.006) were unique independent prognostic indicators of DFS/PFS and OS, respectively. CONCLUSION: (18)F-FDG PET/CT may potentially predict tumor PD-L1 expression and play a role in predicting prognosis of PD-L1/PD-1 immunotherapy in lung adenocarcinoma.
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spelling pubmed-73945112020-08-13 PD-L1 in Lung Adenocarcinoma: Insights into the Role of (18)F-FDG PET/CT Cui, Yan Li, Xuena Du, Bulin Diao, Yao Li, Yaming Cancer Manag Res Original Research PURPOSE: This study aimed to evaluate the role of (18)F-fluorodeoxyglucose ((18)F-FDG) positron emission tomography (PET)/computed tomography (CT) in expression of tumor programmed death ligand-1 (PD-L1) expression and prognostic significance of (18)F-FDG PET/CT at different PD-L1 status in patients with lung adenocarcinoma. PATIENTS AND METHODS: Seventy-three patients with primary lung adenocarcinoma who received (18)F-FDG PET/CT before treatment were retrospectively included in this study. Expression of tumor PD-L1, programmed death-1 (PD-1) and glucose metabolic parameters were evaluated. RESULTS: Tumor PD-L1 expression was positively correlated with maximum standardized uptake value (SUVmax), total lesion glycolysis (TLG), hexokinase II (HK-II) and glucose transporter 1 (GLUT-1) (P<0.0001 for all). SUVmax was a unique independent predictor of tumor PD-L1 expression, with an optimal cut-off value of 9.5. For all the patients, tumor stage (P<0.001) and SUVmax (P=0.009) were independent prognostic indicators of disease-free survival (DFS)/progression-free survival (PFS) while carcino-embryonic antigen (CEA) (P=0.003), Ki67 (P=0.042), PD-L1 (P=0.048) and TLG (P=0.004) were independent prognostic indicators of overall survival (OS). Tumor stage (P=0.004) and SUVmax (P=0.022) were independent prognostic indicators of DFS/PFS while TLG (P=0.012) and CEA (P=0.045) were independent prognostic indicators of OS in the PD-L1-positive group. In the PD-L1-negative group, tumor stage (P=0.002) and CEA (P=0.006) were unique independent prognostic indicators of DFS/PFS and OS, respectively. CONCLUSION: (18)F-FDG PET/CT may potentially predict tumor PD-L1 expression and play a role in predicting prognosis of PD-L1/PD-1 immunotherapy in lung adenocarcinoma. Dove 2020-07-27 /pmc/articles/PMC7394511/ /pubmed/32801879 http://dx.doi.org/10.2147/CMAR.S256871 Text en © 2020 Cui et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Cui, Yan
Li, Xuena
Du, Bulin
Diao, Yao
Li, Yaming
PD-L1 in Lung Adenocarcinoma: Insights into the Role of (18)F-FDG PET/CT
title PD-L1 in Lung Adenocarcinoma: Insights into the Role of (18)F-FDG PET/CT
title_full PD-L1 in Lung Adenocarcinoma: Insights into the Role of (18)F-FDG PET/CT
title_fullStr PD-L1 in Lung Adenocarcinoma: Insights into the Role of (18)F-FDG PET/CT
title_full_unstemmed PD-L1 in Lung Adenocarcinoma: Insights into the Role of (18)F-FDG PET/CT
title_short PD-L1 in Lung Adenocarcinoma: Insights into the Role of (18)F-FDG PET/CT
title_sort pd-l1 in lung adenocarcinoma: insights into the role of (18)f-fdg pet/ct
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7394511/
https://www.ncbi.nlm.nih.gov/pubmed/32801879
http://dx.doi.org/10.2147/CMAR.S256871
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