Optimal Lymphadenectomy in Patients with Well-Differentiated Nonfunctioning Pancreatic Neuroendocrine Neoplasms

Author:

Shintakuya Ryuta1ORCID,Uemura Kenichiro1ORCID,Sumiyoshi Tatsuaki1,Okada Kenjiro1,Baba Kenta1,Harada Takumi1,Murakami Yoshiaki2,Serikawa Masahiro3ORCID,Ishii Yasutaka3ORCID,Arihiro Koji4,Takahashi Shinya1

Affiliation:

1. Department of Surgery, Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima 739-8526, Japan

2. Department of Advanced Medicine, Hiroshima University, Hiroshima 739-8526, Japan

3. Department of Gastroenterology, Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima 739-8526, Japan

4. Department of Anatomical Pathology, Hiroshima University, Hiroshima 739-8526, Japan

Abstract

This study aimed to evaluate the optimal extent of lymphadenectomy in patients with nonfunctioning pancreatic neuroendocrine neoplasms. We retrospectively analyzed the clinicopathological data of patients with nonfunctioning pancreatic neuroendocrine neoplasms who underwent surgical resection. We investigated the frequency of metastases at each lymph node station according to tumor location and analyzed the factors contributing to poor overall survival (OS) and disease-free survival (DFS). Overall, data of 84 patients were analyzed. Among patients with pancreatic head tumors, metastases at stations 8, 13, and 17 were found in one (3.1%), four (12.5%), and three (9.3%) patients, respectively. However, none of the other stations showed metastases. For pancreatic body and tail tumors, metastases only at station 11 were found in two (5.1%) patients. Additionally, multivariate DFS and OS analyses showed that lymph node metastasis was the only independent prognostic factor. In conclusion, lymph node metastasis near the primary tumor was the only independent factor of poor prognosis in patients with nonfunctioning pancreatic neuroendocrine neoplasms after undergoing curative surgery. Peri-pancreatic lymphadenectomy might be recommended for nonfunctioning pancreatic neuroendocrine neoplasms.

Publisher

MDPI AG

Subject

General Medicine

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