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(18)F‑fluorodeoxyglucose positron emission tomography predicts recurrence and histological grade of extrahepatic bile duct cancer
Malignant tumors in cholangiocarcinoma are diagnosed and staged using (18)F-fluorodeoxyglucose positron emission tomography (FDG-PET) and clinical analysis. However, comprehensive analysis, including pathological analysis, has not yet been sufficiently performed. In the present study, the maximum st...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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D.A. Spandidos
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9950358/ https://www.ncbi.nlm.nih.gov/pubmed/36844626 http://dx.doi.org/10.3892/ol.2023.13711 |
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author | Yachi, Takafumi Yoshizawa, Tadashi Kimura, Norihisa Seino, Hiroko Morohashi, Satoko Goto, Shintaro Ishido, Keinosuke Kijima, Hiroshi Hakamada, Kenichi |
author_facet | Yachi, Takafumi Yoshizawa, Tadashi Kimura, Norihisa Seino, Hiroko Morohashi, Satoko Goto, Shintaro Ishido, Keinosuke Kijima, Hiroshi Hakamada, Kenichi |
author_sort | Yachi, Takafumi |
collection | PubMed |
description | Malignant tumors in cholangiocarcinoma are diagnosed and staged using (18)F-fluorodeoxyglucose positron emission tomography (FDG-PET) and clinical analysis. However, comprehensive analysis, including pathological analysis, has not yet been sufficiently performed. In the present study, the maximum standardized uptake value (SUVmax) was calculated using FDG-PET and its relationship with clinicopathological factors was analyzed. The present study included 86 patients who underwent preoperative FDG-PET/computed tomography (CT) and did not receive chemotherapy among 331 patients with hilar and distal cholangiocarcinoma. Receiver operating characteristic analysis with recurrence events was used to determine the SUVmax cutoff of 4.9. Immunohistochemical staining of glucose transporter 1 (Glut1), hypoxia-inducible factor-1α and Ki-67 was performed for pathological analysis. The standardized uptake value (SUV)-high group (SUVmax ≥4.9) had a higher postoperative recurrence rate (P<0.046) and higher Glut1 and Ki-67 expression rates (P<0.05 and P<0.0001, respectively). Furthermore, SUVmax and Glut1 expression (r=0.298; P<0.01) and SUVmax and Ki-67 expression rates (r=0.527; P<0.0001) were positively correlated. The preoperative measurement of SUVmax by PET-CT is useful in predicting recurrence as well as cancer malignancy. |
format | Online Article Text |
id | pubmed-9950358 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-99503582023-02-25 (18)F‑fluorodeoxyglucose positron emission tomography predicts recurrence and histological grade of extrahepatic bile duct cancer Yachi, Takafumi Yoshizawa, Tadashi Kimura, Norihisa Seino, Hiroko Morohashi, Satoko Goto, Shintaro Ishido, Keinosuke Kijima, Hiroshi Hakamada, Kenichi Oncol Lett Articles Malignant tumors in cholangiocarcinoma are diagnosed and staged using (18)F-fluorodeoxyglucose positron emission tomography (FDG-PET) and clinical analysis. However, comprehensive analysis, including pathological analysis, has not yet been sufficiently performed. In the present study, the maximum standardized uptake value (SUVmax) was calculated using FDG-PET and its relationship with clinicopathological factors was analyzed. The present study included 86 patients who underwent preoperative FDG-PET/computed tomography (CT) and did not receive chemotherapy among 331 patients with hilar and distal cholangiocarcinoma. Receiver operating characteristic analysis with recurrence events was used to determine the SUVmax cutoff of 4.9. Immunohistochemical staining of glucose transporter 1 (Glut1), hypoxia-inducible factor-1α and Ki-67 was performed for pathological analysis. The standardized uptake value (SUV)-high group (SUVmax ≥4.9) had a higher postoperative recurrence rate (P<0.046) and higher Glut1 and Ki-67 expression rates (P<0.05 and P<0.0001, respectively). Furthermore, SUVmax and Glut1 expression (r=0.298; P<0.01) and SUVmax and Ki-67 expression rates (r=0.527; P<0.0001) were positively correlated. The preoperative measurement of SUVmax by PET-CT is useful in predicting recurrence as well as cancer malignancy. D.A. Spandidos 2023-02-09 /pmc/articles/PMC9950358/ /pubmed/36844626 http://dx.doi.org/10.3892/ol.2023.13711 Text en Copyright: © Yachi et al. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Articles Yachi, Takafumi Yoshizawa, Tadashi Kimura, Norihisa Seino, Hiroko Morohashi, Satoko Goto, Shintaro Ishido, Keinosuke Kijima, Hiroshi Hakamada, Kenichi (18)F‑fluorodeoxyglucose positron emission tomography predicts recurrence and histological grade of extrahepatic bile duct cancer |
title | (18)F‑fluorodeoxyglucose positron emission tomography predicts recurrence and histological grade of extrahepatic bile duct cancer |
title_full | (18)F‑fluorodeoxyglucose positron emission tomography predicts recurrence and histological grade of extrahepatic bile duct cancer |
title_fullStr | (18)F‑fluorodeoxyglucose positron emission tomography predicts recurrence and histological grade of extrahepatic bile duct cancer |
title_full_unstemmed | (18)F‑fluorodeoxyglucose positron emission tomography predicts recurrence and histological grade of extrahepatic bile duct cancer |
title_short | (18)F‑fluorodeoxyglucose positron emission tomography predicts recurrence and histological grade of extrahepatic bile duct cancer |
title_sort | (18)f‑fluorodeoxyglucose positron emission tomography predicts recurrence and histological grade of extrahepatic bile duct cancer |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9950358/ https://www.ncbi.nlm.nih.gov/pubmed/36844626 http://dx.doi.org/10.3892/ol.2023.13711 |
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