The role of somatostatin analogues in the treatment of neuroendocrine tumours.

Neuroendocrine tumours belong to a heterogeneous family of neoplasms, originating in endocrine glands (such as the pituitary, parathyroid or the neuroendocrine adrenal glands), in endocrine islets (within the thyroid or pancreas) as well as in endocrine cells dispersed between exocrine cells through...

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Main Authors: Grozinsky-Glasberg, S, Grossman, AB, Korbonits, M
Format: Journal article
Language:English
Published: 2008
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author Grozinsky-Glasberg, S
Grossman, AB
Korbonits, M
author_facet Grozinsky-Glasberg, S
Grossman, AB
Korbonits, M
author_sort Grozinsky-Glasberg, S
collection OXFORD
description Neuroendocrine tumours belong to a heterogeneous family of neoplasms, originating in endocrine glands (such as the pituitary, parathyroid or the neuroendocrine adrenal glands), in endocrine islets (within the thyroid or pancreas) as well as in endocrine cells dispersed between exocrine cells throughout the digestive or respiratory tracts. The clinical behaviour of neuroendocrine tumours is variable; they may be functioning or not functioning, ranging from well-differentiated slow growing neuroendocrine tumours to poorly differentiated neuroendocrine tumours, which are highly aggressive malignant tumours. The development of somatostatin analogues as important diagnostic and treatment tools have revolutionised the clinical management of patients with neuroendocrine tumours. However, although symptomatic relief and stabilisation of tumour growth for various periods of time are observed in many patients treated with somatostatin analogues, tumour regression is rare. Development of new somatostatin analogues and new drug combination therapies should further improve the clinical management of these patients.
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spelling oxford-uuid:f84fc65c-a163-4b2a-95de-9b0bca258cfb2022-03-27T12:49:19ZThe role of somatostatin analogues in the treatment of neuroendocrine tumours.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:f84fc65c-a163-4b2a-95de-9b0bca258cfbEnglishSymplectic Elements at Oxford2008Grozinsky-Glasberg, SGrossman, ABKorbonits, MNeuroendocrine tumours belong to a heterogeneous family of neoplasms, originating in endocrine glands (such as the pituitary, parathyroid or the neuroendocrine adrenal glands), in endocrine islets (within the thyroid or pancreas) as well as in endocrine cells dispersed between exocrine cells throughout the digestive or respiratory tracts. The clinical behaviour of neuroendocrine tumours is variable; they may be functioning or not functioning, ranging from well-differentiated slow growing neuroendocrine tumours to poorly differentiated neuroendocrine tumours, which are highly aggressive malignant tumours. The development of somatostatin analogues as important diagnostic and treatment tools have revolutionised the clinical management of patients with neuroendocrine tumours. However, although symptomatic relief and stabilisation of tumour growth for various periods of time are observed in many patients treated with somatostatin analogues, tumour regression is rare. Development of new somatostatin analogues and new drug combination therapies should further improve the clinical management of these patients.
spellingShingle Grozinsky-Glasberg, S
Grossman, AB
Korbonits, M
The role of somatostatin analogues in the treatment of neuroendocrine tumours.
title The role of somatostatin analogues in the treatment of neuroendocrine tumours.
title_full The role of somatostatin analogues in the treatment of neuroendocrine tumours.
title_fullStr The role of somatostatin analogues in the treatment of neuroendocrine tumours.
title_full_unstemmed The role of somatostatin analogues in the treatment of neuroendocrine tumours.
title_short The role of somatostatin analogues in the treatment of neuroendocrine tumours.
title_sort role of somatostatin analogues in the treatment of neuroendocrine tumours
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