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....

Full description

Bibliographic Details
Main Authors: Paola Di Giacinto, Francesca Rota, Laura Rizza, Davide Campana, Andrea Isidori, Andrea Lania, Andrea Lenzi, Paolo Zuppi, Roberto Baldelli
Format: Article
Language:English
Published: Hindawi Limited 2018-01-01
Series:International Journal of Endocrinology
Online Access:http://dx.doi.org/10.1155/2018/8126087
id doaj-aacb9c272a264c8ca0992e445ddb2c1a
record_format Article
spelling 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
work_keys_str_mv AT paoladigiacinto chromograninafromlaboratorytoclinicalaspectsofpatientswithneuroendocrinetumors
AT francescarota chromograninafromlaboratorytoclinicalaspectsofpatientswithneuroendocrinetumors
AT laurarizza chromograninafromlaboratorytoclinicalaspectsofpatientswithneuroendocrinetumors
AT davidecampana chromograninafromlaboratorytoclinicalaspectsofpatientswithneuroendocrinetumors
AT andreaisidori chromograninafromlaboratorytoclinicalaspectsofpatientswithneuroendocrinetumors
AT andrealania chromograninafromlaboratorytoclinicalaspectsofpatientswithneuroendocrinetumors
AT andrealenzi chromograninafromlaboratorytoclinicalaspectsofpatientswithneuroendocrinetumors
AT paolozuppi chromograninafromlaboratorytoclinicalaspectsofpatientswithneuroendocrinetumors
AT robertobaldelli chromograninafromlaboratorytoclinicalaspectsofpatientswithneuroendocrinetumors
_version_ 1724841216046006272