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: Bronchial neuroendocrine neoplasms (NENs) can be subdivided into TCs, ACs and neuroendocrine carcinomas (NECs). Although a few studies have explored treatment approaches and oncological outcomes, most focus on surgical cohorts, small sample sizes, or mixed groups including TC, AC, and NECs. Real-life cohort data are lacking.
Conference:
Presenting Author: Clement D
Authors: Correia J, Sarker D, Dolly S, Frydman A, Srirajaskanthan R,
Keywords: bronchial carcinoid, treatment pattern, recurrence-free survival, overall survival,
Introduction: Benign insulinomas are the main cause of endogenous hyperinsulinemic hypoglycaemia (EHH) in adults, with surgery as the only cure. Pancreas-preserving procedures are preferred, making precise localisation crucial. Recent studies indicate that GLP-1R imaging, such as [68Ga]Ga-DOTA-exendin-4 (68Ga-Ex4) PET/CT, outperforms conventional imaging in identifying insulinomas.
Conference:
Presenting Author: Fricke J
Authors: Fricke J, Laubner K, Schildmeijer M, Menz L, Christ E,
Keywords: GLP1-Receptor PET/CT, Insulinoma, nesidioblatosis, endogenous hyperinsulinemic hypoglycaemia, real-life data,
#4556 Optimising the establishment of patient-derived models for neuroendocrine neoplasms
Introduction: Neuroendocrine neoplasms (NENs) are clinically and molecularly diverse, with limited understanding of their tumour biology. Efforts to develop patient-derived models have been unsuccessful, highlighting an urgent need for accurate models to support fundamental research.
Conference:
Presenting Author: Hernández Llorens M
Authors: Hernández-Llorens M, Baena-Moreno M, Lamas-Paz A, Sarmentero J, Anton-Pascual B,
Keywords: patient-derived model, organoids, PDXs, Growth factor,
#4449 Treatment of MiNEN with peptide receptor radionuclide therapy
Introduction: Mixed non-neuroendocrine and neuroendocrine neoplasms (MiNENs) of gastrointestinal tract are rare tumours with characteristic histological features include at least 30% of both neuroendocrine and non-neuroendocrine components of the whole neoplasm. They are usually treated with surgical resection and chemotherapy in advanced disease. However, there is scarcity of data for the use of peptide receptor radionuclide therapy (PRRT) in these tumours.
Conference:
Presenting Author: Shekhda K
Authors: Shekhda K, Luong T, Paterson A, Navalkissoor S, Krell D,
#4410 NETest can predict the tumour burden in neuroendocrine tumours
Introduction: Neuroendocrine tumours (NETs) are rare malignancies characterised by slow growth and a lack of reliable biomarkers for predicting tumour burden, treatment response, and prognosis.
Conference:
Presenting Author: