Chromogranin A: From Laboratory to Clinical Aspects of Patients with Neuroendocrine Tumors
Background. Neuroendocrine tumors (NETs) are characterized by having behavior and prognosis that depend upon tumor histology, primary site, staging, and proliferative index. The symptoms associated with carcinoid syndrome and vasoactive intestinal peptide tumors are treated with octreotide acetate....
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doaj-aacb9c272a264c8ca0992e445ddb2c1a2020-11-25T02:27:43ZengHindawi LimitedInternational Journal of Endocrinology1687-83371687-83452018-01-01201810.1155/2018/81260878126087Chromogranin A: From Laboratory to Clinical Aspects of Patients with Neuroendocrine TumorsPaola Di Giacinto0Francesca Rota1Laura Rizza2Davide Campana3Andrea Isidori4Andrea Lania5Andrea Lenzi6Paolo Zuppi7Roberto Baldelli8Endocrinological Oncology, Service of Endocrinology, A.O. San Camillo-Forlanini, Rome, ItalyEndocrinological Oncology, Service of Endocrinology, A.O. San Camillo-Forlanini, Rome, ItalyEndocrinological Oncology, Service of Endocrinology, A.O. San Camillo-Forlanini, Rome, ItalyDepartment of Medical and Surgical Sciences, S. Orsola-Malpighi University Hospital, Bologna, ItalyDepartment of Experimental Medicine, Sapienza University of Rome, Rome, ItalyDepartment of Endocrinology, Humanitas Clinical and Research Center, Humanitas University, Milan, ItalyDepartment of Experimental Medicine, Sapienza University of Rome, Rome, ItalyEndocrinological Oncology, Service of Endocrinology, A.O. San Camillo-Forlanini, Rome, ItalyEndocrinological Oncology, Service of Endocrinology, A.O. San Camillo-Forlanini, Rome, ItalyBackground. Neuroendocrine tumors (NETs) are characterized by having behavior and prognosis that depend upon tumor histology, primary site, staging, and proliferative index. The symptoms associated with carcinoid syndrome and vasoactive intestinal peptide tumors are treated with octreotide acetate. The PROMID trial assesses the effect of octreotide LAR on the tumor growth in patients with well-differentiated metastatic midgut NETs. The CLARINET trial evaluates the effects of lanreotide in patients with nonfunctional, well-, or moderately differentiated metastatic enteropancreatic NETs. Everolimus has been approved for the treatment of advanced pancreatic NETs (pNETs) based on positive PFS effects, obtained in the treated group. Sunitinib is approved for the treatment of patients with progressive gastrointestinal stromal tumor or intolerance to imatinib, because a randomized study demonstrated that it improves PFS and overall survival in patients with advanced well-differentiated pNETs. In a phase II trial, pasireotide shows efficacy and tolerability in the treatment of patients with advanced NETs, whose symptoms of carcinoid syndrome were resistant to octreotide LAR. An open-label, phase II trial assesses the clinical activity of long-acting repeatable pasireotide in treatment-naive patients with metastatic grade 1 or 2 NETs. Even if the growth of the neoplasm was significantly inhibited, it is still unclear whether its antiproliferative action is greater than that of octreotide and lanreotide. Because new therapeutic options are needed to counter the natural behavior of neuroendocrine tumors, it would also be useful to have a biochemical marker that can be addressed better in the management of these patients. Chromogranin A is currently the most useful biomarker to establish diagnosis and has some utility in predicting disease recurrence, outcome, and efficacy of therapy.http://dx.doi.org/10.1155/2018/8126087 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Paola Di Giacinto Francesca Rota Laura Rizza Davide Campana Andrea Isidori Andrea Lania Andrea Lenzi Paolo Zuppi Roberto Baldelli |
spellingShingle |
Paola Di Giacinto Francesca Rota Laura Rizza Davide Campana Andrea Isidori Andrea Lania Andrea Lenzi Paolo Zuppi Roberto Baldelli Chromogranin A: From Laboratory to Clinical Aspects of Patients with Neuroendocrine Tumors International Journal of Endocrinology |
author_facet |
Paola Di Giacinto Francesca Rota Laura Rizza Davide Campana Andrea Isidori Andrea Lania Andrea Lenzi Paolo Zuppi Roberto Baldelli |
author_sort |
Paola Di Giacinto |
title |
Chromogranin A: From Laboratory to Clinical Aspects of Patients with Neuroendocrine Tumors |
title_short |
Chromogranin A: From Laboratory to Clinical Aspects of Patients with Neuroendocrine Tumors |
title_full |
Chromogranin A: From Laboratory to Clinical Aspects of Patients with Neuroendocrine Tumors |
title_fullStr |
Chromogranin A: From Laboratory to Clinical Aspects of Patients with Neuroendocrine Tumors |
title_full_unstemmed |
Chromogranin A: From Laboratory to Clinical Aspects of Patients with Neuroendocrine Tumors |
title_sort |
chromogranin a: from laboratory to clinical aspects of patients with neuroendocrine tumors |
publisher |
Hindawi Limited |
series |
International Journal of Endocrinology |
issn |
1687-8337 1687-8345 |
publishDate |
2018-01-01 |
description |
Background. Neuroendocrine tumors (NETs) are characterized by having behavior and prognosis that depend upon tumor histology, primary site, staging, and proliferative index. The symptoms associated with carcinoid syndrome and vasoactive intestinal peptide tumors are treated with octreotide acetate. The PROMID trial assesses the effect of octreotide LAR on the tumor growth in patients with well-differentiated metastatic midgut NETs. The CLARINET trial evaluates the effects of lanreotide in patients with nonfunctional, well-, or moderately differentiated metastatic enteropancreatic NETs. Everolimus has been approved for the treatment of advanced pancreatic NETs (pNETs) based on positive PFS effects, obtained in the treated group. Sunitinib is approved for the treatment of patients with progressive gastrointestinal stromal tumor or intolerance to imatinib, because a randomized study demonstrated that it improves PFS and overall survival in patients with advanced well-differentiated pNETs. In a phase II trial, pasireotide shows efficacy and tolerability in the treatment of patients with advanced NETs, whose symptoms of carcinoid syndrome were resistant to octreotide LAR. An open-label, phase II trial assesses the clinical activity of long-acting repeatable pasireotide in treatment-naive patients with metastatic grade 1 or 2 NETs. Even if the growth of the neoplasm was significantly inhibited, it is still unclear whether its antiproliferative action is greater than that of octreotide and lanreotide. Because new therapeutic options are needed to counter the natural behavior of neuroendocrine tumors, it would also be useful to have a biochemical marker that can be addressed better in the management of these patients. Chromogranin A is currently the most useful biomarker to establish diagnosis and has some utility in predicting disease recurrence, outcome, and efficacy of therapy. |
url |
http://dx.doi.org/10.1155/2018/8126087 |
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