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Hepatic blood flow by perfusion computed tomography as an imaging biomarker for patients with gastric cancer

Perfusion computed tomography (PCT) is a less invasive imaging modality that provides information about tissue hemodynamics at the capillary level. The present study aimed to investigate the correlation between hepatic perfusion and gastric cancer progression. A total of 136 patients with gastric ad...

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Autores principales: Shuto, Kiyohiko, Mori, Mikito, Kosugi, Chihiro, Narushima, Kazuo, Nakabayashi, Satoko, Fujisiro, Takeshi, Sato, Asami, Hayano, Koichi, Shimizu, Hiroaki, Koda, Keiji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6396202/
https://www.ncbi.nlm.nih.gov/pubmed/30867759
http://dx.doi.org/10.3892/ol.2019.9969
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author Shuto, Kiyohiko
Mori, Mikito
Kosugi, Chihiro
Narushima, Kazuo
Nakabayashi, Satoko
Fujisiro, Takeshi
Sato, Asami
Hayano, Koichi
Shimizu, Hiroaki
Koda, Keiji
author_facet Shuto, Kiyohiko
Mori, Mikito
Kosugi, Chihiro
Narushima, Kazuo
Nakabayashi, Satoko
Fujisiro, Takeshi
Sato, Asami
Hayano, Koichi
Shimizu, Hiroaki
Koda, Keiji
author_sort Shuto, Kiyohiko
collection PubMed
description Perfusion computed tomography (PCT) is a less invasive imaging modality that provides information about tissue hemodynamics at the capillary level. The present study aimed to investigate the correlation between hepatic perfusion and gastric cancer progression. A total of 136 patients with gastric adenocarcinoma were evaluated in the present study. Prior to initial treatment, liver PCT was performed across the hepatic hilar plane and the hepatic blood flow (HBF) was measured using the dual-input deconvolution method. HBF was compared with clinicopathological factors, patient prognosis and circulating serum proangiogenic cytokines. The median HBF was 217 ml/min/100 g tissue. Patients with high HBF had larger tumors (43 mm vs. 71, P<0.001) and more advanced tumor-node stages (P<0.001 for both). When both patient groups of operable and inoperable were compared by their respective median HBF values, each high-HBF group had a significantly worse prognosis (P=0.002 and P=0.024), notably in the inoperable group, with <1-year survival. In 17 postoperative recurrent patients, the high-HBF at recurrence group also had a significantly worse postrecurrent prognosis (P=0.019). HBF was an independent prognostic factor (hazard ratio, 2.019; P=0.048) and was strongly associated with serum vascular endothelial growth factor level (R=0.607, P<0.001). HBF was significantly correlated with gastric cancer progression, and is an easily measured imaging biomarker reflecting patient survival.
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spelling pubmed-63962022019-03-13 Hepatic blood flow by perfusion computed tomography as an imaging biomarker for patients with gastric cancer Shuto, Kiyohiko Mori, Mikito Kosugi, Chihiro Narushima, Kazuo Nakabayashi, Satoko Fujisiro, Takeshi Sato, Asami Hayano, Koichi Shimizu, Hiroaki Koda, Keiji Oncol Lett Articles Perfusion computed tomography (PCT) is a less invasive imaging modality that provides information about tissue hemodynamics at the capillary level. The present study aimed to investigate the correlation between hepatic perfusion and gastric cancer progression. A total of 136 patients with gastric adenocarcinoma were evaluated in the present study. Prior to initial treatment, liver PCT was performed across the hepatic hilar plane and the hepatic blood flow (HBF) was measured using the dual-input deconvolution method. HBF was compared with clinicopathological factors, patient prognosis and circulating serum proangiogenic cytokines. The median HBF was 217 ml/min/100 g tissue. Patients with high HBF had larger tumors (43 mm vs. 71, P<0.001) and more advanced tumor-node stages (P<0.001 for both). When both patient groups of operable and inoperable were compared by their respective median HBF values, each high-HBF group had a significantly worse prognosis (P=0.002 and P=0.024), notably in the inoperable group, with <1-year survival. In 17 postoperative recurrent patients, the high-HBF at recurrence group also had a significantly worse postrecurrent prognosis (P=0.019). HBF was an independent prognostic factor (hazard ratio, 2.019; P=0.048) and was strongly associated with serum vascular endothelial growth factor level (R=0.607, P<0.001). HBF was significantly correlated with gastric cancer progression, and is an easily measured imaging biomarker reflecting patient survival. D.A. Spandidos 2019-03 2019-01-25 /pmc/articles/PMC6396202/ /pubmed/30867759 http://dx.doi.org/10.3892/ol.2019.9969 Text en Copyright: © Shuto et al. 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
Shuto, Kiyohiko
Mori, Mikito
Kosugi, Chihiro
Narushima, Kazuo
Nakabayashi, Satoko
Fujisiro, Takeshi
Sato, Asami
Hayano, Koichi
Shimizu, Hiroaki
Koda, Keiji
Hepatic blood flow by perfusion computed tomography as an imaging biomarker for patients with gastric cancer
title Hepatic blood flow by perfusion computed tomography as an imaging biomarker for patients with gastric cancer
title_full Hepatic blood flow by perfusion computed tomography as an imaging biomarker for patients with gastric cancer
title_fullStr Hepatic blood flow by perfusion computed tomography as an imaging biomarker for patients with gastric cancer
title_full_unstemmed Hepatic blood flow by perfusion computed tomography as an imaging biomarker for patients with gastric cancer
title_short Hepatic blood flow by perfusion computed tomography as an imaging biomarker for patients with gastric cancer
title_sort hepatic blood flow by perfusion computed tomography as an imaging biomarker for patients with gastric cancer
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6396202/
https://www.ncbi.nlm.nih.gov/pubmed/30867759
http://dx.doi.org/10.3892/ol.2019.9969
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