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Staging FDG PET-CT changes management in patients with gastric adenocarcinoma who are eligible for radical treatment

AIM: 18-fluorodeoxyglucose positron emission tomography-computed tomography (FDG PET-CT) is valuable in the management of patients with oesophageal cancer, but a role in gastric cancer staging is debated. Our aim was to review the role of FDG PET-CT in a large gastric cancer cohort in a tertiary UK...

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Autores principales: Bosch, Karen D., Chicklore, Sugama, Cook, Gary J., Davies, Andrew R., Kelly, Mark, Gossage, James A., Baker, Cara R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7075833/
https://www.ncbi.nlm.nih.gov/pubmed/31377821
http://dx.doi.org/10.1007/s00259-019-04429-x
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author Bosch, Karen D.
Chicklore, Sugama
Cook, Gary J.
Davies, Andrew R.
Kelly, Mark
Gossage, James A.
Baker, Cara R.
author_facet Bosch, Karen D.
Chicklore, Sugama
Cook, Gary J.
Davies, Andrew R.
Kelly, Mark
Gossage, James A.
Baker, Cara R.
author_sort Bosch, Karen D.
collection PubMed
description AIM: 18-fluorodeoxyglucose positron emission tomography-computed tomography (FDG PET-CT) is valuable in the management of patients with oesophageal cancer, but a role in gastric cancer staging is debated. Our aim was to review the role of FDG PET-CT in a large gastric cancer cohort in a tertiary UK centre. METHODS: We retrospectively reviewed data from 330 patients presenting with gastric adenocarcinoma between March 2014 and December 2016 of whom 105 underwent pre-treatment staging FDG PET-CT scans. FDG PET-CT scans were graded qualitatively and quantitatively (SUV(max)) and compared with staging diagnostic CT and operative pathology results (n = 30) in those undergoing resection. RESULTS: Of the 105 patients (74 M, median age 73 years) 86% of primary tumours were metabolically active (uptake greater than normal stomach) on FDG PET-CT [41/44 (93%) of the intestinal histological subtype (SUV(max) 14.1 ± 1.3) compared to 36/46 (78%) of non-intestinal types (SUV(max) 9.0 ± 0.9), p = 0.005]. FDG PET-CT upstaged nodal or metastastic staging of 20 patients (19%; 13 intestinal, 6 non-intestinal, 1 not reported), with 17 showing distant metastases not evident on other imaging. On histological analysis, available in 30 patients, FDG PET-CT showed low sensitivity (40%) but higher specificity (73%) for nodal involvement. CONCLUSION: FDG PET-CT provides new information in a clinically useful proportion of patients, which leads to changes in treatment strategy, most frequently by detecting previously unidentified metastases, particularly in those with intestinal-type tumours.
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spelling pubmed-70758332020-03-23 Staging FDG PET-CT changes management in patients with gastric adenocarcinoma who are eligible for radical treatment Bosch, Karen D. Chicklore, Sugama Cook, Gary J. Davies, Andrew R. Kelly, Mark Gossage, James A. Baker, Cara R. Eur J Nucl Med Mol Imaging Original Article AIM: 18-fluorodeoxyglucose positron emission tomography-computed tomography (FDG PET-CT) is valuable in the management of patients with oesophageal cancer, but a role in gastric cancer staging is debated. Our aim was to review the role of FDG PET-CT in a large gastric cancer cohort in a tertiary UK centre. METHODS: We retrospectively reviewed data from 330 patients presenting with gastric adenocarcinoma between March 2014 and December 2016 of whom 105 underwent pre-treatment staging FDG PET-CT scans. FDG PET-CT scans were graded qualitatively and quantitatively (SUV(max)) and compared with staging diagnostic CT and operative pathology results (n = 30) in those undergoing resection. RESULTS: Of the 105 patients (74 M, median age 73 years) 86% of primary tumours were metabolically active (uptake greater than normal stomach) on FDG PET-CT [41/44 (93%) of the intestinal histological subtype (SUV(max) 14.1 ± 1.3) compared to 36/46 (78%) of non-intestinal types (SUV(max) 9.0 ± 0.9), p = 0.005]. FDG PET-CT upstaged nodal or metastastic staging of 20 patients (19%; 13 intestinal, 6 non-intestinal, 1 not reported), with 17 showing distant metastases not evident on other imaging. On histological analysis, available in 30 patients, FDG PET-CT showed low sensitivity (40%) but higher specificity (73%) for nodal involvement. CONCLUSION: FDG PET-CT provides new information in a clinically useful proportion of patients, which leads to changes in treatment strategy, most frequently by detecting previously unidentified metastases, particularly in those with intestinal-type tumours. Springer Berlin Heidelberg 2019-08-03 2020 /pmc/articles/PMC7075833/ /pubmed/31377821 http://dx.doi.org/10.1007/s00259-019-04429-x Text en © The Author(s) 2019 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Article
Bosch, Karen D.
Chicklore, Sugama
Cook, Gary J.
Davies, Andrew R.
Kelly, Mark
Gossage, James A.
Baker, Cara R.
Staging FDG PET-CT changes management in patients with gastric adenocarcinoma who are eligible for radical treatment
title Staging FDG PET-CT changes management in patients with gastric adenocarcinoma who are eligible for radical treatment
title_full Staging FDG PET-CT changes management in patients with gastric adenocarcinoma who are eligible for radical treatment
title_fullStr Staging FDG PET-CT changes management in patients with gastric adenocarcinoma who are eligible for radical treatment
title_full_unstemmed Staging FDG PET-CT changes management in patients with gastric adenocarcinoma who are eligible for radical treatment
title_short Staging FDG PET-CT changes management in patients with gastric adenocarcinoma who are eligible for radical treatment
title_sort staging fdg pet-ct changes management in patients with gastric adenocarcinoma who are eligible for radical treatment
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7075833/
https://www.ncbi.nlm.nih.gov/pubmed/31377821
http://dx.doi.org/10.1007/s00259-019-04429-x
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