Mixed Neuroendocrine and Non-neuroendocrine Tumor of Pancreato-Biliary Origin Treated Successfully with Peptide Receptor Radionuclide Therapy
- 23 June 2025
- journal article
- case report
- Published by Springer Nature in Journal of Gastrointestinal Cancer
- Vol. 56 (1) , 140
Abstract
Mixed neuroendocrine and non-neuroendocrine neoplasms (MiNENs) are rare neoplasms composed of morphologically distinguishable neuroendocrine (NE) and non-neuroendocrine components, each representing at least 30% of the tumor volume. The NE component must be substantiated by immunohistochemistry. MiNENs generally have a poor prognosis, with a more aggressive component dictating overall survival and prognosis. Owing to its rarity, there are no specific validated treatment guidelines available for these tumors, and they are generally treated with surgery if possible. However, surgically unresectable or advanced tumors are generally treated with chemotherapy. We report a case of an elderly woman who was referred to the neuroendocrine tumor (NET) unit following incidental findings of liver lesions found on cardiac magnetic resonance imaging (MRI) performed for an asymptomatic heart murmur. Histology from the liver biopsy revealed MiNEN with up to 60% grade 2 (Ki67: 19%) well-differentiated NET and up to 30% well-differentiated to moderately differentiated adenocarcinoma of possible pancreato-biliary origin; intrahepatic ductal primary could not be excluded. Her 18-fluoro-deoxyglucose positron emission tomography (FDG-PET) revealed no FDG-avid lesions, and a 68Gallium 1,4,7,10-tetraazacyclododecane-tetraacetic acid Tyr3-octreotate (68 Ga-DOTATATE)-PET scan revealed multiple areas of intensely DOTATATE-avid liver lesions. Due to the absence of any primary imaging findings, the patient was diagnosed with MiNEN of possible pancreato-biliary origin. She was started on lanreotide 120 mg every 28 days for 6 months, with no response to the treatment. Subsequently, the patient was treated with four cycles of 177Lutetium-DOTATATE (Lutathera®) peptide receptor radionuclide therapy (PRRT). She tolerated the treatment well, with no significant side effects. MRI at the end of treatment revealed a partial response to treatment. PRRT is currently not used in treatment protocols for the management of MiNENs; however, it could be considered a treatment option in patients with MiNENs, where there is a predominant component of well-differentiated NETs with 68 Ga-DOTATATE avid lesions.Keywords
This publication has 31 references indexed in Scilit:
- Clinicopathologic Study of 62 Acinar Cell Carcinomas of the PancreasAmerican Journal of Surgical Pathology, 2012
- Metastatic mixed acinar‐neuroendocrine carcinoma of the pancreas to the liver: A cytopathology case report with review of the literatureDiagnostic Cytopathology, 2011
- Mixed Ductal-Endocrine Carcinoma of the Pancreas Occurring as a Double Cancer: Report of a CaseInternational Surgery, 2011
- A case of mixed ductal-endocrine carcinoma of the pancreasMedical Molecular Morphology, 2011
- Mixed ductal‐endocrine carcinoma derived from intraductal papillary mucinous neoplasm (IPMN) of the pancreas identified by human telomerase reverse transcriptase (hTERT) expressionJournal of Surgical Oncology, 2007
- Mixed exocrine-endocrine tumor of the pancreas.2005
- Mixed ductal-endocrine carcinomas of the pancreas and ductal adenocarcinomas with scattered endocrine cells: characterization of the endocrine cellsVirchows Archiv, 2003
- Mixed ductal–pancreatic polypeptide‐cell carcinoma of the pancreasHistopathology, 2002
- Mixed exocrine-endocrine tumors of the pancreas.2000
- Mixed ductal-endocrine carcinoma of the pancreas presenting as gastrinoma with Zollinger-Ellison syndrome: an autopsy case with a 24-year survival periodVirchows Archiv, 1999