Results 51 to 60 of about 393,422 (164)

Real-World Effectiveness of Capecitabine and Temozolomide Across Endocrine and Neuroendocrine Neoplasm Subtypes (ENENs): A Population-Based Cohort Study from Alberta, Canada (2011–2021)

open access: yesCurrent Oncology
Capecitabine plus temozolomide (CAPTEM) improves progression-free survival (PFS) in pancreatic endocrine and neuroendocrine neoplasms (PNENs), yet its real-world effectiveness across other endocrine and neuroendocrine neoplasm (ENEN) subtypes remains ...
Alda Aleksi   +7 more
doaj   +1 more source

Rare breast and subcutaneous metastases from pancreatic neuroendocrine tumor: a case report

open access: yesWorld Journal of Surgical Oncology, 2019
Background Neuroendocrine tumors are a group of rare neoplasms, and the pancreatic neuroendocrine tumors (PNETs) represent only 1–2% of all pancreatic malignant tumors.
Dorotea Bosco   +5 more
doaj   +1 more source

Discovery and Optimization of AMT‐676, a CDH17‐Targeting ADC for the Treatment of Advanced Gastrointestinal Cancers

open access: yesAdvanced Science, EarlyView.
AMT‐676 is a novel antibody‐drug conjugate targeting CDH17, an adhesion molecule uniquely exposed on gastrointestinal tumor surfaces. Engineered with an optimized exatecan payload, it demonstrates profound tumor regression and a robust bystander effect across diverse preclinical models.
Ying‐nan Wang   +21 more
wiley   +1 more source

Endoscopic Ultrasound-Guided Ablation of Focal Pancreatic Lesions: The GRUPUGE Perspective

open access: yesGE: Portuguese Journal of Gastroenterology, 2020
Focal pancreatic lesions include a heterogeneous group of solid and cystic lesions, with different natures and variable clinical, imagiological, and pathological characteristics.
Miguel Bispo   +6 more
doaj   +1 more source

Pancreatic neuroendocrine neoplasms : from genetics to everolimus resistance [PDF]

open access: yes, 2021
Pancreatic neuroendocrine neoplasms are rare tumors of which the genetic constitution is not fully understood. In addition, resistance against everolimus, a frequently used treatment modality, forms a clinical challenge in these tumors.
Vandamme, TAL   +2 more
core   +1 more source

A rare presentation of an ACTH‐producing high‐grade large cell neuroendocrine carcinoma with Cushing’s syndrome

open access: yesClinical Case Reports, 2021
High‐grade neuroendocrine tumors (HGNET) are rare neoplasms composed of neural and hormonal with only around 42 cases reported in the last 20 years1.
Francis Essien   +5 more
doaj   +1 more source

Pancreatic neuroendocrine tumours: a comparison of cytological classification systems. [PDF]

open access: yes
Aims: Cytological classification systems provide a standardised interpretation framework for reporting cytological specimens. Three well-known classification systems can be applied when reporting pancreatic cytology.
Hanks, Matthew   +6 more
core   +1 more source

Advanced Imaging of Pancreatic Neoplasms

open access: yes, 2022
Imaging has a pivotal role in pancreatic neoplasms, ranging from diagnosis to treatment monitor. It is crucial, especially for pancreatic ductal adenocarcinoma (PDAC), to obtain an early diagnosis, since the therapeutic approach is mainly surgical and ...
Cardobi N., De Robertis R., D'Onofrio M.
core   +1 more source

Multidisciplinary treatment of pancreatic neuroendocrine neoplasm with portal vein thrombosis and multiple liver metastases by minimally invasive surgical and neoadjuvant therapy

open access: yesJournal of Pancreatology
The treatment of patients with pancreatic neuroendocrine neoplasms accompanied by metastasis is complex and highly individualized. This article reports a 43-year-old male patient diagnosed with a neuroendocrine tumor on the pancreatic tail combined with ...
Hao Chen   +4 more
doaj   +1 more source

Surgical management of pancreatic neuroendocrine neoplasms

open access: yesAnnals of Saudi Medicine, 2014
Pancreatic neuroendocrine neoplasms are relatively rare entities, representing approximately 1% to 2% of all pancreatic tumors. Owing to their rarity as well as their relatively indolent natural history, treatment approaches are not yet standardized.
Stefano Partelli   +5 more
doaj   +1 more source

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