Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2020 Aug 15;18(1):208.
doi: 10.1186/s12957-020-01994-6.

A single-center experience with pancreatic cystic neuroendocrine tumors

Affiliations

A single-center experience with pancreatic cystic neuroendocrine tumors

Ange Khalil et al. World J Surg Oncol. .

Abstract

Background: Pancreatic neuroendocrine tumors (PNET) are rare, with a significant malignant potential. This study aimed to determine outcomes of patients with resected PNETs according to the cystic component and confirm the accuracy of preoperative staging.

Methods: From 1997 to 2016, 106 patients underwent resection of PNETs, including 73 purely solid (S-PNETs, 69%), 21 mixed (M-PNETs, 20%), and 12 purely cystic lesions (C-PNETs, 11%). To ensure consistent comparisons of overall (OS) and disease-free (DFS) survival outcomes between the 3 groups, the patients were matched according to the World Health Organization (WHO) grade and tumor height.

Results: Overall, the rate of correlation between the preoperative and pathological diagnoses was low in the C-PNET group (33%, P = 0.03). None of the 24 patients (23%) with metastatic disease at the time of surgery were in the C-PNET group. Furthermore, significantly more parenchyma-sparing resections (P = 0.039) and fewer enlarged resections (P = 0.019) were achieved in the C-PNET group. C-PNET group had a significantly lower node invasion rate than the S-PNET and M-PNET groups (8% vs. 41% and 24%, P = 0.004). Although median OS was comparable in all 3 groups before (P = 0.3) and after (P = 0.18) matching, higher median DFS was observed in the C-PNET group than in the other groups after matching (P = 0.038).

Conclusion: C-PNET was associated with a better prognosis than PNET with a solid component. The results support a wait-and-see policy in cases wherein a reliable preoperative diagnosis remains challenging.

Keywords: Cystic component; Pancreatic neuroendocrine tumor; Survival.

PubMed Disclaimer

Conflict of interest statement

The authors declare that they have no competing interests.

Figures

Fig. 1
Fig. 1
Overall survival after matching
Fig. 2
Fig. 2
Disease-free survival after matching

References

    1. Lykoudis PM, Partelli S, Muffatti F, et al. Treatment challenges in and outside a specialist network setting: pancreatic neuroendocrine tumours. Eur J Surg Oncol. 2019;45:46–51. doi: 10.1016/j.ejso.2017.08.019. - DOI - PubMed
    1. Metz DC, Jensen RT. Gastrointestinal neuroendocrine tumors: pancreatic endocrine tumors. Gastroenterology. 2008;135(5):1469–1492. doi: 10.1053/j.gastro.2008.05.047. - DOI - PMC - PubMed
    1. Modlin IM, Oberg K, Chung DC, et al. Gastroenteropancreatic neuroendocrine tumours. Lancet Oncol. 2008;9:61–72. doi: 10.1016/S1470-2045(07)70410-2. - DOI - PubMed
    1. Paiella S, Marchegiani G, Miotto M, et al. Are cystic pancreatic neuroendocrine tumors an indolent entity results from a single-center surgical series. Neuroendocrinology. 2018;106:234–241. doi: 10.1159/000477849. - DOI - PubMed
    1. Singhi AD, Chu LC, Tatsas AD, et al. Cystic pancreatic neuroendocrine tumors: a clinicopathologic study. Am J Surg Pathol. 2012;36:1666–1673. doi: 10.1097/PAS.0b013e31826a0048. - DOI - PubMed