Abstract Library
Welcome to the open-access search for all ENETS abstracts presented at the Annual ENETS Conferences.
Everyone can browse the library to find basic information on abstracts. To get full access to each entry, you will be asked to log in to your myENETS account.
ENETS Abstract Search
Introduction: Everolimus monotherapy provided a limited median progression-free survival (PFS) for gastroenteropancreatic neuroendocrine tumours (GEP-NETs), there remains a necessity for better therapeutic approaches.
Conference:
Presenting Author:
Authors: Hijioka S, Honma Y, Machida N, Mizuno N, Hamaguchi T,
Keywords: everolimus, lanreotide, PFS, RCT,
Introduction: Patients with metastatic gastroenteropancreatic neuroendocrine tumours (GEP-NET) have limited therapeutic options.
Conference:
Presenting Author:
Authors: Capdevila J, Amthauer H, Ansquer C, Deshayes E, Garcia-Carbonero R,
Keywords: radiopharmaceutical therapy, neuroendocrine tumour, [177Lu]Lu-edotreotide, progression-free survival, gastroenteropancreatic,
Introduction: Everolimus, an mTOR inhibitor, has demonstrated efficacy in NET treatment. Orlistat, used primarily for obesity management, inhibits fat absorption. This study investigates the potential synergistic effects of Everolimus combined with Orlistat on the development of NETs.
Conference:
Presenting Author:
Keywords: Everolimus, orlistat, mTOR, PI3K/Akt, signalling pathway,
Introduction: PNET is a rare group of highly heterogeneous tumours with neuroendocrine differentiation properties. Everolimus is the most promising drug for progressive well-differentiated pNETs. Sorafenib's anti-tumour activity may involve regulation of the mTOR pathway.
Conference:
Presenting Author: Zheng H
Authors: Zheng H,
Keywords: sorafenib, everolimus, pancreatic neuroendocrine tumour, mTOR,
Introduction: Everolimus 10mg PO daily is approved for patients (pts) with advanced G1/G2 neuroendocrine tumours (NET) but is associated with significant toxicity, including 20% of serious infections in real-world pts. In phase I trials, 5mg/day was sufficient to inhibit the mTOR pathway. Retrospective data suggest that 5mg/day is similarly effective to 10mg/day but less toxic.
Conference:
Presenting Author:
Authors: Riechelmann R, Campos A, Durant L, Bulzico D,
Keywords: everolimus, neuroendocrine tumour, dose optimisation, toxicity,