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Clinically determined type of (18)F-fluoro-2-deoxyglucose uptake as an alternative prognostic marker in resectable pancreatic cancer

PURPOSE: To investigate the association between clinical PET (positron emission tomography) type and oncologic outcome in resectable pancreatic cancer. METHODS: Between January 2008 and October 2012, patients who underwent potentially curative resection for resectable pancreatic ductal adenocarcinom...

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Autores principales: Chong, Jae Uk, Hwang, Ho Kyoung, Lee, Jin Ho, Yun, Mijin, Kang, Chang Moo, Lee, Woo Jung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5325284/
https://www.ncbi.nlm.nih.gov/pubmed/28235029
http://dx.doi.org/10.1371/journal.pone.0172606
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author Chong, Jae Uk
Hwang, Ho Kyoung
Lee, Jin Ho
Yun, Mijin
Kang, Chang Moo
Lee, Woo Jung
author_facet Chong, Jae Uk
Hwang, Ho Kyoung
Lee, Jin Ho
Yun, Mijin
Kang, Chang Moo
Lee, Woo Jung
author_sort Chong, Jae Uk
collection PubMed
description PURPOSE: To investigate the association between clinical PET (positron emission tomography) type and oncologic outcome in resectable pancreatic cancer. METHODS: Between January 2008 and October 2012, patients who underwent potentially curative resection for resectable pancreatic ductal adenocarcinoma without neoadjuvant treatment were retrospectively investigated. Clinical PET type was defined as follows: pancreatic cancer with similar (18)FDG uptake to renal calyx was determined as kidney-type (K-type), and relatively lower (18)FDG uptake than that of renal calyx was regarded as Non-K type. RESULTS: A total of 53 patients were enrolled. After agreement-based reclassification, agreement based K-type (aK-type) was noted in 34 patients (64.2%), and agreement based Non-K type (aNon K-type) was found in 19 patients (35.8%). There was a significant difference between aK-type and aNon K-type pancreatic cancer (tumor size (P = 0.030), adjusted CA 19–9 (P = 0.007), maximum standard uptake value (SUV(max),P<0.001), metabolic tumor volume (MTV(2.5), P<0.001), total lesion glycolysis (TLG, P<0.001)). K-type pancreatic cancer (n = 31) showed a significantly shorter disease-free time compared with Non-K type (n = 16) (10.8 vs. 24.1 months, P = 0.013). It was also noted that aK-type showed inferior disease-free survival to that of aNon-K type pancreatic cancer (11.9 vs. 28.6 months, P = 0.012). CONCLUSIONS: Clinical PET type is a reliable clinical marker to estimate aggressive tumor biology and can be utilized in predicting tumor recurrence and necessity for postoperative chemotherapy.
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spelling pubmed-53252842017-03-09 Clinically determined type of (18)F-fluoro-2-deoxyglucose uptake as an alternative prognostic marker in resectable pancreatic cancer Chong, Jae Uk Hwang, Ho Kyoung Lee, Jin Ho Yun, Mijin Kang, Chang Moo Lee, Woo Jung PLoS One Research Article PURPOSE: To investigate the association between clinical PET (positron emission tomography) type and oncologic outcome in resectable pancreatic cancer. METHODS: Between January 2008 and October 2012, patients who underwent potentially curative resection for resectable pancreatic ductal adenocarcinoma without neoadjuvant treatment were retrospectively investigated. Clinical PET type was defined as follows: pancreatic cancer with similar (18)FDG uptake to renal calyx was determined as kidney-type (K-type), and relatively lower (18)FDG uptake than that of renal calyx was regarded as Non-K type. RESULTS: A total of 53 patients were enrolled. After agreement-based reclassification, agreement based K-type (aK-type) was noted in 34 patients (64.2%), and agreement based Non-K type (aNon K-type) was found in 19 patients (35.8%). There was a significant difference between aK-type and aNon K-type pancreatic cancer (tumor size (P = 0.030), adjusted CA 19–9 (P = 0.007), maximum standard uptake value (SUV(max),P<0.001), metabolic tumor volume (MTV(2.5), P<0.001), total lesion glycolysis (TLG, P<0.001)). K-type pancreatic cancer (n = 31) showed a significantly shorter disease-free time compared with Non-K type (n = 16) (10.8 vs. 24.1 months, P = 0.013). It was also noted that aK-type showed inferior disease-free survival to that of aNon-K type pancreatic cancer (11.9 vs. 28.6 months, P = 0.012). CONCLUSIONS: Clinical PET type is a reliable clinical marker to estimate aggressive tumor biology and can be utilized in predicting tumor recurrence and necessity for postoperative chemotherapy. Public Library of Science 2017-02-24 /pmc/articles/PMC5325284/ /pubmed/28235029 http://dx.doi.org/10.1371/journal.pone.0172606 Text en © 2017 Chong et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Chong, Jae Uk
Hwang, Ho Kyoung
Lee, Jin Ho
Yun, Mijin
Kang, Chang Moo
Lee, Woo Jung
Clinically determined type of (18)F-fluoro-2-deoxyglucose uptake as an alternative prognostic marker in resectable pancreatic cancer
title Clinically determined type of (18)F-fluoro-2-deoxyglucose uptake as an alternative prognostic marker in resectable pancreatic cancer
title_full Clinically determined type of (18)F-fluoro-2-deoxyglucose uptake as an alternative prognostic marker in resectable pancreatic cancer
title_fullStr Clinically determined type of (18)F-fluoro-2-deoxyglucose uptake as an alternative prognostic marker in resectable pancreatic cancer
title_full_unstemmed Clinically determined type of (18)F-fluoro-2-deoxyglucose uptake as an alternative prognostic marker in resectable pancreatic cancer
title_short Clinically determined type of (18)F-fluoro-2-deoxyglucose uptake as an alternative prognostic marker in resectable pancreatic cancer
title_sort clinically determined type of (18)f-fluoro-2-deoxyglucose uptake as an alternative prognostic marker in resectable pancreatic cancer
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5325284/
https://www.ncbi.nlm.nih.gov/pubmed/28235029
http://dx.doi.org/10.1371/journal.pone.0172606
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