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: Tumour dose may be an important predictor of clinical response, but estimation of a clinically relevant tumour-absorbed dose without high risk of toxicity is challenging.
Conference:
Presenting Author: Gomez Sanchez D
Authors: Gomez Sanchez D, Ribelles M, Fernandez Iglesias A, Paruta Araez L, Mata E,
Keywords: dosimetry, 177Lu-DOTATATE,
Introduction: Evidence for immunotherapy (IT) in patients (pts) with MTC is limited and has shown modest activity.
Conference:
Presenting Author:
Authors: García-Álvarez A, Molina-Cerrillo J, Castelo B, Plana M, Iglesias L,
Keywords: Medullary thyroid carcinoma, Immunotherapy, durvalumab, tremelimumab, anti PD-L1, anti CTLA-4,
Introduction: Adrenocortical carcinoma (ACC) is a rare tumor with a poor prognosis in stage IV with only one treatment regimen of chemotherapy (CT), etoposide, doxorubicin, and cisplatin (EDP) and mitotane with proven activity in a phase 3 trial.
Conference:
Presenting Author:
Authors: Álvarez-Escolá C, Ballester I, Garcia Donas J, Paja M, Iglesias C,
Keywords: Adrenocortical cancer, mitotane, chemotherapy, survival, registry,
Introduction: Ga68-DOTATOC PET/CT enables the detection of cells with overexpression of somatostatin receptors, especially subtypes 2 and 5. This is the basis for its use in the study of neuroendocrine tumors (NETs). Detection of a higher number of lesions is not necessarily followed by a modification of therapeutic approach. From our point of view this is the main success of this technique the impact in the management of these patients.
Conference: 18th Annual ENETS Concerence (2021)
Presenting Author:
Authors: Suarez-Piñera M, Domenech B, Rivera E, Visa L, Iglesias M,
Keywords: Ga68-DOTATOC PET/CT, clinical management,
Introduction: Pherochromocytoma (PH) and paraganglioma (PG) are neuroendocrine tumors arising in cromaffin cells in the adrenal medulla or extra adrenal paraganglia respectively. Clinical presentation is diverse. All PG/PH have malignant potential. Hereditary cases comprise up to 40% of all PG/PH.
Conference: 17th Annual ENETSConcerence (2020)
Presenting Author:
Authors: Dioca M, Calabretta M, Iglesias L, Rojas Bilbao E, Califano I,
Keywords: Pherochromocytoma and paraganglioma (PG),