Abstract Library
Welcome to the open-access search for all ENETS abstracts presented at the Annual ENETS Conferences.
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#3895 NGS in G1-G2 pancreatic NETs – Data collection at University Hospital of Verona
Introduction: Pancreatic neuroendocrine tumors (pNETs) are known to have few druggable gene alterations. One possible area of interest concerns the possibility of giving better biological connotations to the >10% subgroup.
Conference:
Presenting Author: Borghesani M
Authors: Borghesani M, Mafficini A, Luchini C, Scarpa A, Milella M,
Keywords: NGS, neuroendocrine, pancreatic,
Introduction: Rare tumors of the pancreas represent orphan neoplasms. Better knowledge of their biology will allow more effective treatments to be offered to affected patients.
Conference:
Presenting Author: Trevisani E
Authors: Trevisani E, Mafficini A, Benini L, Borghesani M, Rossi A,
Keywords: Precision medicine, rare pancreas, NGS, gene mutation, MiNEN,
Introduction: Exceptional Responders are defined as patients who achieve complete (CR) or partial response (PR) for at least 6 months to a treatment with population PR or CR rate less than 10%, or patients with CR or PR lasting more than three times the median duration of response.
Conference:
Presenting Author: Torresan I
Authors: Torresan I, Mafficini A, Benini L, Borghesani M, Moscarda V,
Keywords: pNET, NGS, G3, everolimus, TSC2,
Introduction: In pancreatic neuroendocrine tumors (PanNETs), there has recently been advancement in understanding the heterogeneity (metastases-like primary; MLP-1/2, intermediate, and insulinoma subtypes) and immunological landscapes. Immunotherapies provide modest therapeutic benefits to patients, which may be linked to low mutational neoantigen loads in PanNETs.
Conference:
Presenting Author: Sadanandam A
Authors: Sadanandam A, Lawlor R, Larkeryd A, Mahalingam A, Mafficini A,
Keywords: Pancreatic neuroendocrine tumor, isoform switching, subtype, mutation, neoantigens, splice variant, spliceosomal mutation, immunotherapy, immunosuppression,
Introduction: Non-functional pancreatic neuroendocrine tumors (PanNETs) are heterogeneous with at least two transcriptome subtypes with differential biology, immune mechanisms and prognosis. However, it is challenging to understand how multimodal data interact with clinical variables and contribute to the disease heterogeneity and phenotypes.
Conference: 18th Annual ENETS Concerence (2021)
Presenting Author: Sadanandam A
Authors: Sadanandam A, Lawlor R, Mafficini A, Luchini C, Nyamundanda G,
Keywords: pancreatic neuroendocrine tumor, multimodal data integration, multiomics, clinical data integration, machine learning, artificial intelligence, subtypes, pancreatic cancer, phenotypes, PhenMap, mutations, gene expression, microRNA,