Loading…

Pancreatic neuroendocrine tumors: Surgical outcomes and survival analysis

Pancreatic neuroendocrine tumors are rare, with rising incidence and limited clinicopathological studies. Adult patients with pNET at a single tertiary care center were retrospectively evaluated. In total, 87 patients with histologically confirmed pNET who underwent resection were evaluated. 11% of...

Full description

Saved in:
Bibliographic Details
Published in:The American journal of surgery 2021-03, Vol.221 (3), p.529-533
Main Authors: Fahmy, Joseph N., Varsanik, M. Alyssa, Hubbs, Daniel, Eguia, Emanuel, Abood, Gerard, Knab, Lawrence M.
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Pancreatic neuroendocrine tumors are rare, with rising incidence and limited clinicopathological studies. Adult patients with pNET at a single tertiary care center were retrospectively evaluated. In total, 87 patients with histologically confirmed pNET who underwent resection were evaluated. 11% of patients had functioning pNETs: 9 insulinoma and 1 VIPoma. The majority (88.5%) were nonfunctioning. The most common surgical procedure performed was distal pancreatectomy with splenectomy (36.8%). 35.6% of cases were performed with minimally invasive surgery (MIS). MIS patients had fewer postoperative complications, shorter length of stay, and fewer ICU admissions.Disease-free survival (DFS) was unaffected by tumor size (p = 0.5) or lymph node status (p = 0.62). Patients with high-grade (G3) tumors experienced significantly shorter DFS (p = 0.02). This series demonstrates that survival in patients with pNET is driven mostly by tumor grade, though overall most have long-term survival after surgical resection. Additionally, an MIS approach is efficacious in appropriately selected cases. Survival for pancreatic neuroendocrine tumors is driven mostly by tumor grade. Minimally invasive surgery is a safe and effective approach to resecting these tumors.
ISSN:0002-9610
1879-1883
DOI:10.1016/j.amjsurg.2020.12.037