Clinicopathological heterogeneity between primary and metastatic sites of gastroenteropancreatic neuroendocrine neoplasm

Abstract Background Chromogranin A (CgA), synaptophysin (Syn) and the Ki-67 index play significant roles in diagnosis or the evaluation of the proliferative activity of gastroenteropancreatic neuroendocrine neoplasms (GEP-NENs). However, little is known about whether these biological markers change...

Full description

Bibliographic Details
Main Authors: Huiying Shi, Chen Jiang, Qin Zhang, Cuihua Qi, Hailing Yao, Rong Lin
Format: Article
Language:English
Published: BMC 2020-09-01
Series:Diagnostic Pathology
Subjects:
Online Access:http://link.springer.com/article/10.1186/s13000-020-01030-x
_version_ 1818970353340252160
author Huiying Shi
Chen Jiang
Qin Zhang
Cuihua Qi
Hailing Yao
Rong Lin
author_facet Huiying Shi
Chen Jiang
Qin Zhang
Cuihua Qi
Hailing Yao
Rong Lin
author_sort Huiying Shi
collection DOAJ
description Abstract Background Chromogranin A (CgA), synaptophysin (Syn) and the Ki-67 index play significant roles in diagnosis or the evaluation of the proliferative activity of gastroenteropancreatic neuroendocrine neoplasms (GEP-NENs). However, little is known about whether these biological markers change during tumor metastasis and whether such changes have effect on prognosis. Methods We analyzed 35 specimens of both primary and metastatic tumor from 779 patients who had been diagnosed as GEP-NENs at Wuhan Union Hospital from August 2011 to October 2019. The heterogeneity of CgA, Syn and Ki-67 index was evaluated by immunohistochemical analysis. Results Among these 779 patients, the three most common sites of NENs in the digestive tract were the pancreas, rectum and stomach. Metastases were found in 311 (39.9%) patients. Among the 35 patients with both primary and metastatic pathological specimens, differences in the Ki-67 level were detected in 54.3% of the patients, while 37.1% showed a difference in CgA and only 11.4% showed a difference in Syn. Importantly, due to the difference in the Ki-67 index between primary and metastatic lesions, the WHO grade was changed in 8.6% of the patients. In addition, a Kaplan–Meier survival analysis showed that patients with Ki-67 index variation had a shorter overall survival (p = 0.0346), while neither Syn variation nor CgA variation was related to patient survival (p = 0.7194, p = 0.4829). Conclusions Our data indicate that primary and metastatic sites of GEP-NENs may exhibit pathological heterogeneity. Ki-67 index variation is closely related to the poor prognosis of patients with tumor metastasis, but neither Syn variation nor CgA variation is related to patient prognosis. Therefore, clinicopathologic evaluation of the primary tumor and metastatic sites could be helpful for predicting the prognosis.
first_indexed 2024-12-20T14:35:08Z
format Article
id doaj.art-7b00fe6100bd44dfbe7c696144daabed
institution Directory Open Access Journal
issn 1746-1596
language English
last_indexed 2024-12-20T14:35:08Z
publishDate 2020-09-01
publisher BMC
record_format Article
series Diagnostic Pathology
spelling doaj.art-7b00fe6100bd44dfbe7c696144daabed2022-12-21T19:37:29ZengBMCDiagnostic Pathology1746-15962020-09-0115111010.1186/s13000-020-01030-xClinicopathological heterogeneity between primary and metastatic sites of gastroenteropancreatic neuroendocrine neoplasmHuiying Shi0Chen Jiang1Qin Zhang2Cuihua Qi3Hailing Yao4Rong Lin5Department of Gastroenterology, Union Hospital, Tongji Medical College, Huazhong University of Science and TechnologyDepartment of Gastroenterology, Union Hospital, Tongji Medical College, Huazhong University of Science and TechnologyDepartment of Pathology, Union Hospital, Tongji Medical College, Huazhong University of Science and TechnologyDepartment of Gastroenterology, Union Hospital, Tongji Medical College, Huazhong University of Science and TechnologyDepartment of Gastroenterology, Union Hospital, Tongji Medical College, Huazhong University of Science and TechnologyDepartment of Gastroenterology, Union Hospital, Tongji Medical College, Huazhong University of Science and TechnologyAbstract Background Chromogranin A (CgA), synaptophysin (Syn) and the Ki-67 index play significant roles in diagnosis or the evaluation of the proliferative activity of gastroenteropancreatic neuroendocrine neoplasms (GEP-NENs). However, little is known about whether these biological markers change during tumor metastasis and whether such changes have effect on prognosis. Methods We analyzed 35 specimens of both primary and metastatic tumor from 779 patients who had been diagnosed as GEP-NENs at Wuhan Union Hospital from August 2011 to October 2019. The heterogeneity of CgA, Syn and Ki-67 index was evaluated by immunohistochemical analysis. Results Among these 779 patients, the three most common sites of NENs in the digestive tract were the pancreas, rectum and stomach. Metastases were found in 311 (39.9%) patients. Among the 35 patients with both primary and metastatic pathological specimens, differences in the Ki-67 level were detected in 54.3% of the patients, while 37.1% showed a difference in CgA and only 11.4% showed a difference in Syn. Importantly, due to the difference in the Ki-67 index between primary and metastatic lesions, the WHO grade was changed in 8.6% of the patients. In addition, a Kaplan–Meier survival analysis showed that patients with Ki-67 index variation had a shorter overall survival (p = 0.0346), while neither Syn variation nor CgA variation was related to patient survival (p = 0.7194, p = 0.4829). Conclusions Our data indicate that primary and metastatic sites of GEP-NENs may exhibit pathological heterogeneity. Ki-67 index variation is closely related to the poor prognosis of patients with tumor metastasis, but neither Syn variation nor CgA variation is related to patient prognosis. Therefore, clinicopathologic evaluation of the primary tumor and metastatic sites could be helpful for predicting the prognosis.http://link.springer.com/article/10.1186/s13000-020-01030-xGastroenteropancreatic neuroendocrine neoplasms (GEP-NENs)Chromogranin (CgA)Synaptophysin (Syn)Ki-67 indexMetastasisHeterogeneity
spellingShingle Huiying Shi
Chen Jiang
Qin Zhang
Cuihua Qi
Hailing Yao
Rong Lin
Clinicopathological heterogeneity between primary and metastatic sites of gastroenteropancreatic neuroendocrine neoplasm
Diagnostic Pathology
Gastroenteropancreatic neuroendocrine neoplasms (GEP-NENs)
Chromogranin (CgA)
Synaptophysin (Syn)
Ki-67 index
Metastasis
Heterogeneity
title Clinicopathological heterogeneity between primary and metastatic sites of gastroenteropancreatic neuroendocrine neoplasm
title_full Clinicopathological heterogeneity between primary and metastatic sites of gastroenteropancreatic neuroendocrine neoplasm
title_fullStr Clinicopathological heterogeneity between primary and metastatic sites of gastroenteropancreatic neuroendocrine neoplasm
title_full_unstemmed Clinicopathological heterogeneity between primary and metastatic sites of gastroenteropancreatic neuroendocrine neoplasm
title_short Clinicopathological heterogeneity between primary and metastatic sites of gastroenteropancreatic neuroendocrine neoplasm
title_sort clinicopathological heterogeneity between primary and metastatic sites of gastroenteropancreatic neuroendocrine neoplasm
topic Gastroenteropancreatic neuroendocrine neoplasms (GEP-NENs)
Chromogranin (CgA)
Synaptophysin (Syn)
Ki-67 index
Metastasis
Heterogeneity
url http://link.springer.com/article/10.1186/s13000-020-01030-x
work_keys_str_mv AT huiyingshi clinicopathologicalheterogeneitybetweenprimaryandmetastaticsitesofgastroenteropancreaticneuroendocrineneoplasm
AT chenjiang clinicopathologicalheterogeneitybetweenprimaryandmetastaticsitesofgastroenteropancreaticneuroendocrineneoplasm
AT qinzhang clinicopathologicalheterogeneitybetweenprimaryandmetastaticsitesofgastroenteropancreaticneuroendocrineneoplasm
AT cuihuaqi clinicopathologicalheterogeneitybetweenprimaryandmetastaticsitesofgastroenteropancreaticneuroendocrineneoplasm
AT hailingyao clinicopathologicalheterogeneitybetweenprimaryandmetastaticsitesofgastroenteropancreaticneuroendocrineneoplasm
AT ronglin clinicopathologicalheterogeneitybetweenprimaryandmetastaticsitesofgastroenteropancreaticneuroendocrineneoplasm