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Clinical and Prognostic Value of PET/CT Imaging with Combination of (68)Ga-DOTATATE and (18)F-FDG in Gastroenteropancreatic Neuroendocrine Neoplasms
BACKGROUND: To evaluate the clinical and prognostic value of PET/CT with combination of (68)Ga-DOTATATE and (18)F-FDG in gastroenteropancreatic neuroendocrine neoplasms (GEP-NENs). METHOD: 83 patients of GEP-NENs who underwent (68)Ga-DOTATATE and (18)F-FDG PET/CT were enrolled between June 2013 and...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5846381/ https://www.ncbi.nlm.nih.gov/pubmed/29681780 http://dx.doi.org/10.1155/2018/2340389 |
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author | Zhang, Panpan Yu, Jiangyuan Li, Jie Shen, Lin Li, Nan Zhu, Hua Zhai, Shizhen Zhang, Yan Yang, Zhi Lu, Ming |
author_facet | Zhang, Panpan Yu, Jiangyuan Li, Jie Shen, Lin Li, Nan Zhu, Hua Zhai, Shizhen Zhang, Yan Yang, Zhi Lu, Ming |
author_sort | Zhang, Panpan |
collection | PubMed |
description | BACKGROUND: To evaluate the clinical and prognostic value of PET/CT with combination of (68)Ga-DOTATATE and (18)F-FDG in gastroenteropancreatic neuroendocrine neoplasms (GEP-NENs). METHOD: 83 patients of GEP-NENs who underwent (68)Ga-DOTATATE and (18)F-FDG PET/CT were enrolled between June 2013 and December 2016. Well-differentiated (WD) NETs are divided into group A (Ki-67 < 10%) and group B (Ki-67 ≥ 10%), and poorly differentiated (PD) NECs are defined as group C. The relationship between PET/CT results and clinicopathological characteristics was retrospectively investigated. RESULT: For groups A/B/C, the sensitivities of (68)Ga-DOTATATE and (18)F-FDG were 78.8%/83.3%/37.5% and 52.0%/72.2%/100.0%. A negative correlation between Ki-67 and SUV(max) of (68)Ga-DOTATATE (R = −0.415; P ≤ 0.001) was observed, while a positive correlation was noted between Ki-67 and SUV(max) of (18)F-FDG (R = 0.683; P ≤ 0.001). 62.5% (5/8) of patients showed significantly more lesions in the bone if (68)Ga-DOTATATE was used, and 22.7% (5/22) of patients showed more lymph node metastases if (18)F-FDG was used. CONCLUSIONS: The sensitivity of dual tracers was correlated with cell differentiation, and a correlation between Ki-67 and both SUV(max) of PET-CTs could be observed. (68)Ga-DOTATATE is suggested for WD-NET and (18)F-FDG is probably suitable for patients with Ki-67 ≥ 10%. |
format | Online Article Text |
id | pubmed-5846381 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-58463812018-04-22 Clinical and Prognostic Value of PET/CT Imaging with Combination of (68)Ga-DOTATATE and (18)F-FDG in Gastroenteropancreatic Neuroendocrine Neoplasms Zhang, Panpan Yu, Jiangyuan Li, Jie Shen, Lin Li, Nan Zhu, Hua Zhai, Shizhen Zhang, Yan Yang, Zhi Lu, Ming Contrast Media Mol Imaging Research Article BACKGROUND: To evaluate the clinical and prognostic value of PET/CT with combination of (68)Ga-DOTATATE and (18)F-FDG in gastroenteropancreatic neuroendocrine neoplasms (GEP-NENs). METHOD: 83 patients of GEP-NENs who underwent (68)Ga-DOTATATE and (18)F-FDG PET/CT were enrolled between June 2013 and December 2016. Well-differentiated (WD) NETs are divided into group A (Ki-67 < 10%) and group B (Ki-67 ≥ 10%), and poorly differentiated (PD) NECs are defined as group C. The relationship between PET/CT results and clinicopathological characteristics was retrospectively investigated. RESULT: For groups A/B/C, the sensitivities of (68)Ga-DOTATATE and (18)F-FDG were 78.8%/83.3%/37.5% and 52.0%/72.2%/100.0%. A negative correlation between Ki-67 and SUV(max) of (68)Ga-DOTATATE (R = −0.415; P ≤ 0.001) was observed, while a positive correlation was noted between Ki-67 and SUV(max) of (18)F-FDG (R = 0.683; P ≤ 0.001). 62.5% (5/8) of patients showed significantly more lesions in the bone if (68)Ga-DOTATATE was used, and 22.7% (5/22) of patients showed more lymph node metastases if (18)F-FDG was used. CONCLUSIONS: The sensitivity of dual tracers was correlated with cell differentiation, and a correlation between Ki-67 and both SUV(max) of PET-CTs could be observed. (68)Ga-DOTATATE is suggested for WD-NET and (18)F-FDG is probably suitable for patients with Ki-67 ≥ 10%. Hindawi 2018-02-26 /pmc/articles/PMC5846381/ /pubmed/29681780 http://dx.doi.org/10.1155/2018/2340389 Text en Copyright © 2018 Panpan Zhang et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Zhang, Panpan Yu, Jiangyuan Li, Jie Shen, Lin Li, Nan Zhu, Hua Zhai, Shizhen Zhang, Yan Yang, Zhi Lu, Ming Clinical and Prognostic Value of PET/CT Imaging with Combination of (68)Ga-DOTATATE and (18)F-FDG in Gastroenteropancreatic Neuroendocrine Neoplasms |
title | Clinical and Prognostic Value of PET/CT Imaging with Combination of (68)Ga-DOTATATE and (18)F-FDG in Gastroenteropancreatic Neuroendocrine Neoplasms |
title_full | Clinical and Prognostic Value of PET/CT Imaging with Combination of (68)Ga-DOTATATE and (18)F-FDG in Gastroenteropancreatic Neuroendocrine Neoplasms |
title_fullStr | Clinical and Prognostic Value of PET/CT Imaging with Combination of (68)Ga-DOTATATE and (18)F-FDG in Gastroenteropancreatic Neuroendocrine Neoplasms |
title_full_unstemmed | Clinical and Prognostic Value of PET/CT Imaging with Combination of (68)Ga-DOTATATE and (18)F-FDG in Gastroenteropancreatic Neuroendocrine Neoplasms |
title_short | Clinical and Prognostic Value of PET/CT Imaging with Combination of (68)Ga-DOTATATE and (18)F-FDG in Gastroenteropancreatic Neuroendocrine Neoplasms |
title_sort | clinical and prognostic value of pet/ct imaging with combination of (68)ga-dotatate and (18)f-fdg in gastroenteropancreatic neuroendocrine neoplasms |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5846381/ https://www.ncbi.nlm.nih.gov/pubmed/29681780 http://dx.doi.org/10.1155/2018/2340389 |
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