Tyrosine kinase inhibitors and immunotherapy updates in neuroendocrine neoplasms
Neuroendocrine tumors (NETs) represent a heterogeneous group of malignancies that arise
from neuroendocrine cells dispersed throughout the organs/tissues of the body. Treatment of …
from neuroendocrine cells dispersed throughout the organs/tissues of the body. Treatment of …
Systemic Therapy for Pancreatic Neuroendocrine Tumors
M Wheless, S Das - Clinical Colorectal Cancer, 2023 - Elsevier
Patients with metastatic or advanced pancreatic neuroendocrine tumors (NETs) carry poorer
prognoses relative to patients with other NETs due to bulkier and often, more proliferative …
prognoses relative to patients with other NETs due to bulkier and often, more proliferative …
Detecting Somatic Mutations for Well-Differentiated Pancreatic Neuroendocrine Tumors in Endoscopic Ultrasound-Guided Fine Needle Aspiration with Next …
Abstract Background Pancreatic neuroendocrine tumors (PanNETs) exhibit heterogenous
behavior, whereby some small tumors are aggressive with a propensity for metastasis …
behavior, whereby some small tumors are aggressive with a propensity for metastasis …
Surgical Management and Long-Term Evaluation of Pancreatic Neuroendocrine Tumors
S Ghabra, B Ramamoorthy, SG Andrews… - Surgical …, 2024 - surgical.theclinics.com
Neuroendocrine tumors (NETs) originate from neuroendocrine cells located in different
organs throughout the body, such as the lung, pancreas, and digestive tract. NETs may …
organs throughout the body, such as the lung, pancreas, and digestive tract. NETs may …
Indications for genetic study in gastro-entero-pancreatic and thoracic neuroendocrine tumors
M Araujo-Castro - Endocrinología, Diabetes y Nutrición (English ed.), 2023 - Elsevier
Abstract Gastro-entero-pancreatic (GEP-NET) and thoracic neuroendocrine tumours (NETs)
are one of the most heritable groups of neoplasms in the body, being multiple endocrine …
are one of the most heritable groups of neoplasms in the body, being multiple endocrine …
Centralization of care for rare genetic syndromes associated with cancer: improving outcomes and advancing research on VHL disease
A Larcher, F Belladelli, F Cei, C Re, I Rowe… - Nature Reviews …, 2024 - nature.com
Abstract Von Hippel–Lindau (VHL) disease is a rare genetic syndrome caused by a
germline pathogenic variant in one VHL allele. Any somatic event disrupting the other allele …
germline pathogenic variant in one VHL allele. Any somatic event disrupting the other allele …
Pancreatic Neuroendocrine Tumors: Signaling Pathways and Epigenetic Regulation
Pancreatic neuroendocrine tumors (PNETs) are characterized by dysregulated signaling
pathways that are crucial for tumor formation and progression. The efficacy of traditional …
pathways that are crucial for tumor formation and progression. The efficacy of traditional …
Molecular alterations and therapeutic targets in pancreatic neuroendocrine tumors
Human pancreatic neuroendocrine tumors (PanNETs) are a rare, deadly tumor type that is
sporadic or arises in the background of a hereditary syndrome. A critical genetic event in …
sporadic or arises in the background of a hereditary syndrome. A critical genetic event in …
Indicaciones de estudio genético en los tumores neuroendocrinos gastro-entero-pancreáticos y torácicos
M Araujo-Castro - Endocrinología, Diabetes y Nutrición, 2023 - Elsevier
Los tumores neuroendocrinos (TNE) gastro-entero-pancreáticos (TNE-GEP) y torácicos son
uno de los grupos de neoplasias más heredables del organismo, siendo el síndrome de …
uno de los grupos de neoplasias más heredables del organismo, siendo el síndrome de …
[HTML][HTML] Transformation of metastatic nonfunctioning pancreatic neuroendocrine tumor into insulinoma—two case reports
Background: Pancreatic neuroendocrine tumors (PanNETs) are rare neoplasms that are
characterized by hormonal symptoms. While most PanNETs are nonfunctional, there have …
characterized by hormonal symptoms. While most PanNETs are nonfunctional, there have …