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: Pancreatic angiosarcoma is a rare and highly aggressive tumour originated from lymphatic or vascular endothelial cells, with poor prognosis and few effective treatments. However, little is known about its tumour microenvironment and the mechanisms of its progression.
Conference:
Presenting Author: Yang Y
Authors: Yang Y, Chen L, Liu M, Lin X, Peng S,
Keywords: pancreatic angiosarcoma, single-cell RNA sequencing, immunotherapy, PD-L1, CD86,
Introduction: In the ZS001 clinical trial, we observed that NET patients with higher PD-L1 expression levels were more likely to benefit preferentially from immunotherapy.
Conference:
Presenting Author:
Authors: Sun Y, Zhang Q, Cao F, Huang X, Zhang P,
Keywords: neuroendocrine tumour, immunotherapy, PD-L1, SP142, 28-8, C0148, E1L3N,
Introduction: NEC is a rare, aggressive cancer with limited response to standard first-line chemo (etoposide + cisplatin/carboplatin, EP/EC).
Conference:
Presenting Author:
Authors: Cao D, Li X, Li R, Wang X, Yang Y,
Keywords: neuroendocrine carcinoma, First-line, chemotherapy, camrelizumab,
#4285 Predictive biomarkers for immunotherapy efficacy in neuroendocrine neoplasms
Introduction: The application of immunotherapy in NENs is still in its early stages. Identifying reliable predictive biomarkers of efficacy is critical for research, enabling better selection of patients who are more likely to respond to immunotherapy and improving treatment success rates.
Conference:
Presenting Author: Liang Y
Authors: Liang Y, Sun Z, Jia X, Chen J,
Keywords: immunotherapy, biomarker, neuroendocrine neoplasm,
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,