Abstract Library
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#4646 Dysregulated miRNA in patients with GEP-NEN and potential role as circulating biomarker
Introduction: Neuroendocrine neoplasms (NENs) are a class of rare and molecularly extremely heterogeneous tumours. NENs arise predominantly in the gastrointestinal (GEP) and pulmonary tracts but can also involve thyroid and breast. NENs often present with non-specific symptoms and lack early specific biomarkers, leading to frequent metastatic diagnoses and primary site challenges.
Conference:
Presenting Author:
Authors: Di Mauro A, Clemente O, Cannella L, Della Vittoria G, Neri G,
Keywords: neuroendocrine tumour, miRNome profiling, biomarker, gep-net, molecular biology,
Introduction: Surgery is the only definitive therapy for neuroendocrine tumours (NET). In number of small intestine NET first symptom is ileus or perforation, lifesaving surgical procedures applied. Such cases have significant risk of recurrence.
Conference:
Presenting Author: Hajac �
Authors: Hajac L, Szewczyk K, Piwkowski P, Chowaniec Z, Mazurak J,
Keywords: radio guided surgery, Neuroendocrine tumour, early relapse,
Introduction: PRRT with 177Lu-DOTATATE is a major treatment for metastatic digestive NETs. Most patients have prolonged progression-free survival, but around 20% experience early progression.
Conference:
Presenting Author: Haissaguerre M
Authors: Haissaguerre M, Hadoux J, Tlili G, Deshayes E, Lacombe M,
Keywords: GEP-NET, PRRT, early tumour progression,
Introduction: Pancreatic neuroendocrine tumours (PanNETs) are the leading cause of death in patients (pts) with MEN1. Screening is recommended to diagnose early and prevent metastases. The optimal cut-off of when to intervene in a PanNET is still an area of debate.
Conference:
Presenting Author: Frydman A
Authors: Frydman A, Clement D, Srirajaskanthan R,
Introduction: Most neuroendocrine neoplasms (NEN) are sporadic. Early disease onset has been increasingly observed in NEN.
Conference:
Presenting Author: Malczewska-Herman A
Authors: Malczewska-Herman A, Pavel M, Rinke A, Holmager P, Opalinska M,
Keywords: neuroendocrine neoplasm, sporadic, young adults, prognosis, survival,