Carcinoid syndrome: updates and review of current therapy
K Oleinikov, S Avniel-Polak, DJ Gross… - … Treatment Options in …, 2019 - Springer
Opinion statement Carcinoid syndrome (CS) is a complex disorder caused by functional
neuroendocrine tumors (NETs). This debilitating disease is characterized by hyper-secretion …
neuroendocrine tumors (NETs). This debilitating disease is characterized by hyper-secretion …
Refractory carcinoid syndrome: a review of treatment options
RP Riechelmann, AA Pereira… - … Advances in Medical …, 2017 - journals.sagepub.com
Carcinoid syndrome (CSy) is a constellation of symptoms that may commonly present in
patients with well differentiated neuroendocrine tumors (NETs), with somatostatin analogs …
patients with well differentiated neuroendocrine tumors (NETs), with somatostatin analogs …
Systemic therapeutic options for carcinoid
M Pavel, M Kidd, I Modlin - Seminars in Oncology, 2013 - Elsevier
“Carcinoids” are mostly slow-growing neuroendocrine neoplasms (NENs) with low
proliferative activity. A wide range of therapeutic options with variable efficacy exist …
proliferative activity. A wide range of therapeutic options with variable efficacy exist …
Control of carcinoid syndrome with everolimus
J Capdevila, ID Miranda, G Obiols… - Annals of …, 2011 - annalsofoncology.org
discussion The therapeutic options for refractory carcinoid syndrome are limited. The
development of new targeted agents for the treatment of neuroendocrine tumors (NET) has …
development of new targeted agents for the treatment of neuroendocrine tumors (NET) has …
Efficacy, safety and unmet needs of evolving medical treatments for carcinoid syndrome
A Koumarianou, K Daskalakis, M Tsoli… - Journal of …, 2022 - Wiley Online Library
This review reports on the currently available medical treatment options for the control of
symptoms due to carcinoid syndrome in patients with neuroendocrine tumors. The efficacy …
symptoms due to carcinoid syndrome in patients with neuroendocrine tumors. The efficacy …
Carcinoid syndrome and neuroendocrine tumours
F Wernig, CN Jayasena, WS Dhillo - Medicine, 2021 - Elsevier
Neuroendocrine tumours (NETs) arise from neuroendocrine cells of the gastrointestinal tract,
pancreas, bronchi or other rare primary sites and comprise a variety of different tumour …
pancreas, bronchi or other rare primary sites and comprise a variety of different tumour …
High-Dose Somatostatin Analogs for the Treatment of Neuroendocrine Neoplasms: where are we Now?
T Alonso-Gordoa, R Manneh, E Grande… - … Treatment Options in …, 2022 - Springer
Opinion statement Neuroendocrine tumors (NET) represent a complex and heterogeneous
group of malignancies arising from the diffuse endocrine cells and other cells derived from …
group of malignancies arising from the diffuse endocrine cells and other cells derived from …
Carcinoid syndrome and neuroendocrine tumours
F Wernig, CN Jayasena, WS Dhillo - Medicine, 2017 - Elsevier
Neuroendocrine tumours (NETs) arise from the gastrointestinal tract, pancreas, bronchi or
other rare primary sites and comprise a variety of different tumour types. Carcinoid tumours …
other rare primary sites and comprise a variety of different tumour types. Carcinoid tumours …
ELECT: A phase 3 study of efficacy and safety of lanreotide autogel/depot (LAN) treatment for carcinoid syndrome in patients with neuroendocrine tumors (NETs).
A Vinik, EM Wolin, H Audry, EL Gomez-Panzani… - 2014 - ascopubs.org
268 Background: Somatostatin analogs (SSAs) are the mainstay treatment for carcinoid
syndrome. LAN is a long-acting SSA approved for this indication in> 50 countries, but not yet …
syndrome. LAN is a long-acting SSA approved for this indication in> 50 countries, but not yet …
Recent Advances in the Diagnosis and Management of Carcinoid Syndrome
N Subash, MM Papali, KP Bahadur, C Avanthika… - Disease-a-Month, 2022 - Elsevier
Carcinoid syndrome, a paraneoplastic condition linked with the release of multiple humoral
factors, affects around 30-40% of patients with well-differentiated neuroendocrine tumours …
factors, affects around 30-40% of patients with well-differentiated neuroendocrine tumours …