Preprint / Version 1

Size alone is not enough: Ki-67 and invasion patterns identify high-risk pancreatic neuroendocrine tumors (pNETs)

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DOI:

https://doi.org/10.1590/0102-672020260000027e1956

Keywords:

Neuroendocrine Tumors, Surgical Oncology, Pancreas, Pancreatectomy

Abstract

Background: Pancreatic neuroendocrine tumors (pNETS) constitute a heterogeneous and rare disease worldwide. Diagnosis has been increasing, and the evaluation of prognostic factors has become even more important in the treatment decision process. Aims: To present results and prognostic factors in patients undergoing surgical treatment for pNETS in a single Brazilian center.

Results: The most performed surgical procedure was corpus-caudal pancreatectomy with splenectomy 60.0%. The median hospital stay was 8 (5-13) days, and postoperative mortality occurred in 1.7%. Overall survival in 3 and 5 years was 93.8% and 92.1%. Disease-free survival at 3 and 5 years was 87.1% and 71.8%. Patients with tumors smaller than 2.0 cm did not present with lymph node disease or recurrence and 2.1-2.5cm individuals had lymph node disease in 11.1% and recurrence in 11.1%. In univariate and multivariate analysis, the presence of lymphatic and perineural vascular invasion and Ki67 (3-20) were strongly correlated with positive lymph node disease and recurrence, respectively.

Conclusions: The presence of lymphatic and perineural vascular invasion, Ki67 (3 to 20), and tumors above 2.5 cm correlated with positive lymph node disease and recurrence.

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Posted

06/16/2026

How to Cite

Size alone is not enough: Ki-67 and invasion patterns identify high-risk pancreatic neuroendocrine tumors (pNETs). (2026). In SciELO Preprints. https://doi.org/10.1590/0102-672020260000027e1956

Section

Biological Sciences

Plaudit

Data statement

  • The research data is available on demand, condition justified in the manuscript