Gastroenteropancreatic neuroendocrine neoplasms: a 10-year experience of a single center

Pol Arch Med Wewn. 2015;125(5):337-46. doi: 10.20452/pamw.2832. Epub 2015 Apr 29.

Abstract

Introduction: Gastroenteropancreatic neuroendocrine neoplasms (GEP-NENs) constitute a rare and heterogeneous group of tumors with varied biology.

Objectives: The aim of this study was to establish the clinical characteristics of patients with GEP-NEN and identify factors influencing their 5-year survival.

Patients and methods: The study included 122 patients living in Kraków or its administrative region, who were diagnosed with GEP-NEN between 2002 and 2011.

Results: The mean follow-up period was 4.9 ±2.8 years. The most frequent primary site of the tumor was the small intestine (n = 25; 20%), followed by pancreas (n = 23; 19%), rectum (n = 23; 19%), stomach (n = 21; 17%), appendix (n = 19; 16%), and colon (n = 11; 9%). There were 84 tumors classified as NEN G1; 31, as NEN G2; 5, as neuroendocrine carcinoma; and 1, as mixed adenoneuroendocrine carcinoma. Most well-differentiated GEP-NENs (n = 57; 57%) were diagnosed at stage I according to the American Joint Committee on Cancer / Union for International Cancer Control (AJCC/UICC) classification; 77% of NEN G1 (n = 64) were diagnosed at stage I, but the majority of NEN G2—at stage IV (n = 18; 58%). Metastases at diagnosis were found in 38 patients (34%). In 90% of the cases (n = 101), tumors were hormonally nonfunctional. The overall 5-year survival was 85%. In the univariate analysis, NEN G2 (P = 0.003), higher stage according to the AJCC/UICC classification (P <0.001), and metastases at diagnosis (P <0.001) were associated with poorer prognosis. In standardized multivariate models, higher stage (P = 0.02) and metastases at diagnosis (P = 0.02) were independent risk factors for death.

Conclusions: The most important factors affecting survival of patients with GEP-NENs are tumor stage and the presence of metastases at diagnosis. The analysis of single-center data improves identification of patients with poorer prognosis requiring a more aggressive approach.

MeSH terms

  • Combined Modality Therapy
  • Female
  • Follow-Up Studies
  • Humans
  • Intestinal Neoplasms / classification*
  • Intestinal Neoplasms / epidemiology
  • Intestinal Neoplasms / pathology*
  • Intestinal Neoplasms / therapy
  • Male
  • Neoplasm Staging
  • Neuroendocrine Tumors / classification*
  • Neuroendocrine Tumors / epidemiology
  • Neuroendocrine Tumors / pathology*
  • Neuroendocrine Tumors / therapy
  • Pancreatic Neoplasms / classification*
  • Pancreatic Neoplasms / epidemiology
  • Pancreatic Neoplasms / pathology*
  • Pancreatic Neoplasms / therapy
  • Poland
  • Prognosis
  • Risk Factors
  • Stomach Neoplasms / classification*
  • Stomach Neoplasms / epidemiology
  • Stomach Neoplasms / pathology*
  • Stomach Neoplasms / therapy
  • Survival Rate

Supplementary concepts

  • Gastro-enteropancreatic neuroendocrine tumor