Abstract Library
Welcome to the open-access search for all ENETS abstracts presented at the Annual ENETS Conferences.
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ENETS Abstract Search
Introduction: Small intestinal neuroendocrine tumours are well-differentiated and express type 2 somatostatin receptors (SSTR2). Treatment with somatostatin analogues (SSA) (octreotide or lanreotide) has been a cornerstone in controlling tumour growth for 25 years. Peptide Receptor Radionuclide Therapy (PRRT), utilising radiolabelled SSA, was introduced in our institution in May 2009 as primarily 2nd line treatment after progression on SSA. The standard PRRT regimen includes 4 cycles of PRRT (7.4 GBq 177Lu-DOTATATE every eight weeks). Re-treatment protocols remain debated.
Conference:
Presenting Author: Andreassen M
Authors: Slott C, Oturai P, Langer S, Møller S, Hansen C,
Keywords: SSA, PRRT, small intestinal NET,
Introduction: Colorectal neuroendocrine carcinoma (CR-NEC) is a rare and aggressive disease. Most cases are metastatic at diagnosis and palliative chemotherapy is the only systemic treatment option.
Conference:
Presenting Author: Morken S
Authors: Morken S, Langer S, Knigge U, Hjortland G, Sundlöv A,
Keywords: neuroendocrine carcinoma, NEC, colorectal, chemotherapy,
Introduction: Small intestinal neuroendocrine tumors (siNET) are one of the most common neuroendocrine neoplasms. Radical surgery is the only curative treatment.
Conference:
Presenting Author: Andreassen M
Authors: Slott C, Langer S, Møller S, Krogh J, Klose M,
Keywords: Small intestinal neuroendocrine tumor survival, prognosis, recurrence,
Introduction: The prognosis and impact of different prognostic factors in pancreatic neuroendocrine neoplasms (pNEN) remains controversial.
Conference:
Presenting Author: Andreassen M
Authors: Møller S, Langer S, Slott C, Krogh J, Palnæs Hansen C,
Keywords: Pancreatic neuroendocrine neoplasms incidence, clinical presentation, prognosis,
#3728 ACTH-secreting pancreatic neuroendocrine neoplasms – A case-series
Introduction: Ectopic Cushing’s syndrome occurs rarely in patients with pancreatic neuroendocrine neoplasms. Early recognition of symptoms is critical given the high morbidity and mortality associated with Cushing’s syndrome.
Conference:
Presenting Author: Al-Toubah T
Authors: Al-Toubah T, Pelle E, Hallanger-Johnson J, Haider M, Strosberg J,
Keywords: pancreatic neuroendocrine neoplasm, Cushing’s syndrome, ACTH, ectopic Cushing’s, neuroendocrine tumor,