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Is Multifocality an Indicator of Aggressive Behavior in Small Bowel Neuroendocrine Tumors?
Journal article   Peer reviewed

Is Multifocality an Indicator of Aggressive Behavior in Small Bowel Neuroendocrine Tumors?

Allen B Choi, Jessica E Maxwell, Kendall J Keck, Andrew J Bellizzi, Joseph S Dillon, Thomas M OʼDorisio and James R Howe
Pancreas, Vol.46(9), pp.1115-1120
10/2017
DOI: 10.1097/MPA.0000000000000911
PMCID: PMC5679126
PMID: 28902780
url
https://www.ncbi.nlm.nih.gov/pmc/articles/5679126View
Open Access

Abstract

Many patients with small bowel neuroendocrine tumors (SBNETs) have multifocal tumors (MFTs), but the frequency of MFTs has varied widely across SBNET studies. It is also unclear whether patients with MFTs have more advanced disease or worse clinical course than do those with unifocal SBNETs. We set out to determine the frequency of multifocal and unifocal SBNETs and compare clinicopathologic factors, somatostatin receptor 2 expression, and survival. Clinicopathologic variables from 179 patients with surgically managed SBNETs were collected. Statistical comparisons were made using Welch t-test, Wilcoxon test, and Fisher's exact test. Survival was assessed using the Kaplan-Meier method. Somatostatin receptor 2 expression was analyzed by quantitative polymerase chain reaction, and Ki-67 expression by immunohistochemistry. Multifocal tumors were found in 45% of patients with SBNETs. Clinicopathologic factors such as grade, TNM stage, presence of distant metastases, mean somatostatin receptor 2 expression, success of imaging modalities, and preoperative and postoperative hormone levels were not significantly different between multifocal and unifocal groups. Progression-free survival and overall survival were also not significantly affected by multifocality. Clinicopathologic features and survival of patients with MFTs and unifocal tumors are remarkably similar. Although the etiology of MFTs is unclear, patients with MFTs do not have a more aggressive clinical course than patients with unifocal SBNETs.
Neuroendocrine Tumors - pathology Intestine, Small - pathology Neuroendocrine Tumors - metabolism Humans Intestinal Neoplasms - metabolism Middle Aged Gene Expression Regulation, Neoplastic Kaplan-Meier Estimate Male Intestinal Neoplasms - pathology Neuroendocrine Tumors - genetics Receptors, Somatostatin - genetics Young Adult Adolescent Aged, 80 and over Adult Female Ki-67 Antigen - biosynthesis Aged Intestine, Small - metabolism Intestinal Neoplasms - genetics

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