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Tumors of the nervous or endocrine system within the pancreas From Wikipedia, the free encyclopedia
Pancreatic neuroendocrine tumours (PanNETs, PETs, or PNETs), often referred to as "islet cell tumours",[1][2] or "pancreatic endocrine tumours"[3][4] are neuroendocrine neoplasms that arise from cells of the endocrine (hormonal) and nervous system within the pancreas.
PanNETs are a type of neuroendocrine tumor, representing about one-third of gastroenteropancreatic neuroendocrine tumors (GEP-NETs). Many PanNETs are benign, while some are malignant. Aggressive PanNET tumors have traditionally been termed "islet cell carcinoma".
PanNETs are quite distinct from the usual form of pancreatic cancer, the majority of which are adenocarcinomas, which arise in the exocrine pancreas. Only 1 or 2% of clinically significant pancreas neoplasms are PanNETs.[5]
The majority of PanNETs are benign, while some are malignant. The World Health Organization (WHO) classification scheme places neuroendocrine tumors into three main categories, which emphasize the tumor grade rather than the anatomical origin.[3] In practice, those tumors termed well or intermediately differentiated PanNETs in the WHO scheme are sometimes called "islet cell tumors". The high-grade subtype termed neuroendocrine cancer (NEC) in the WHO scheme, is synonymous with "islet cell carcinoma".
| Type | Relative incidence | Typical location of tumor[6] | Biomarkers[6] | Symptoms[7] |
|---|---|---|---|---|
| Insulinoma | 35–40%[7] | Head, body, tail of pancreas | insulin, proinsulin, C-peptide | Hypoglycemia |
| Gastrinoma | 16–30%[7] | Gastrinoma triangle | gastrin, PP |
|
| VIPoma | <10%[7] | Distal pancreas (body and tail) | VIP |
|
| Somatostatinoma | <5%[7] | Pancreatoduodenal groove, ampullary, periampullary | somatostatin | |
| PPoma | Head or pancreas | pancreatic polypeptide | ||
| Glucagonoma | 1%[8] | Body and tail of pancreas | glucagon, glycentin |
Relative incidence is given as percentage of all functional pancreatic neuroendocrine tumors.
Some PanNETs do not cause any symptoms, in which case they may be discovered incidentally on a CT scan performed for a different purpose.[10]: 43–44 Symptoms such as abdominal or back pain or pressure, diarrhea, indigestion, or yellowing of the skin and whites of the eyes can arise from the effects of a larger PanNET tumor, either locally or at a metastasis.[11][medical citation needed] About 40%[medical citation needed] of PanNETS have symptoms related to excessive secretion of hormones or active polypeptides and are accordingly labeled as "functional"; the symptoms reflect the type of hormone secreted, as discussed below. Up to 90% [12] of PanNETs are nonsecretory or nonfunctional, in which there is no secretion, or the quantity or type of products, such as pancreatic polypeptide (PPoma), chromogranin A, and neurotensin, do not cause a clinical syndrome although blood levels may be elevated.[13] In total, 85% of PanNETs have an elevated blood marker.[2]
Functional tumors are often classified by the hormone most strongly secreted, for example:
In these various types of functional tumors, the frequency of malignancy and the survival prognosis have been estimated dissimilarly, but a pertinent accessible summary is available.[17]
Because symptoms are non-specific, diagnosis is often delayed.[18]
Measurement of hormones including pancreatic polypeptide, gastrin, proinsulin, insulin, glucagon, and vasoactive intestinal peptide can determine if a tumor is causing hypersecretion.[18][19]
Multiphase CT and MRI are the primary modalities for morphologic imaging of PNETs. While MRI is superior to CT for imaging, both of the primary tumor and evaluation of metastases, CT is more readily available. Notably, while many malignant lesions are hypodense in contrast-enhanced studies, the liver metastases of PNETs are hypervascular and readily visualized in the late arterial phase of the post-contrast CT study. However, morphological imaging alone is not sufficient for a definite diagnosis[18][20]
On biopsy, immunohistochemistry is generally positive for chromogranin and synaptophysin.[21] Genetic testing thereof typically shows altered MEN1 and DAXX/ATRX.[21]
The new 2019 WHO classification and grading criteria for neuroendocrine tumors of the digestive system grades all the neuroendocrine tumors into three grades, based on their degree of cellular differentiation (from well-differentiated NET grade (G)1 to G3, and poorly-differentiated neuroendokrina cancer, NEC G3), morphology, mitotic rate and Ki-67 index.[22] The NCCN recommends the use of the same AJCC-UICC staging system as pancreatic adenocarcinoma.[10]: 52 Using this scheme, the stage by stage outcomes for PanNETs are dissimilar to pancreatic exocrine cancers.[23] A different TNM system for PanNETs has been proposed by The European Neuroendocrine Tumor Society.[24]
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In general, treatment for PanNET encompasses the same array of options as other neuroendocrine tumors, as discussed in that main article. However, there are some specific differences, which are discussed here.[10]
In functioning PanNETs, octreotide is usually recommended prior to biopsy[10]: 21 or surgery[10]: 45 but is generally avoided in insulinomas to avoid profound hypoglycemia.[10]: 69
PanNETs in Multiple endocrine neoplasia type 1 are often multiple, and thus require different treatment and surveillance strategies.[10]
Some PanNETs are more responsive to chemotherapy than are gastroenteric carcinoid tumors. Several agents have shown activity.[16] In well differentiated PanNETs, chemotherapy is generally reserved for when there are no other treatment options. Combinations of several medicines have been used, such as doxorubicin with streptozocin and fluorouracil (5-FU)[16] and capecitabine with temozolomide.[citation needed] Although marginally effective in well-differentiated PETs, cisplatin with etoposide has some activity in poorly differentiated neuroendocrine cancers (PDNECs),[16] particularly if the PDNEC has an extremely high Ki-67 score of over 50%.[10]: 30
Several targeted therapy agents have been approved in PanNETs by the FDA based on improved progression-free survival (PFS):
Pancreatic neuroendocrine tumors may arise in the context of multiple endocrine neoplasia type 1, Von Hippel–Lindau disease, neurofibromatosis type 1 (NF-1) or tuberose sclerosis (TSC)[31][32]
Analysis of somatic DNA mutations in well-differentiated pancreatic neuroendocrine tumors identified four important findings:[33][7]
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