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Elevated chromogranin A (CgA) serum levels in the patients with advanced pancreatic cancer
被引:31
|作者:
Malaguarnera, Michele
[2
]
Cristaldi, Erika
[1
]
Cammalleri, Lisa
[1
]
Colonna, Valentina
[1
]
Lipari, Helga
[1
]
Capici, Alessandra
[1
]
Cavallaro, Andrea
[3
]
Beretta, Massimiliano
[1
]
Alessandria, Innocenza
[1
]
Luca, Salvatore
[1
]
Motta, Massimo
[1
]
机构:
[1] Univ Catania, Cannizzaro Hosp, Dept Senescence Urol & Neurol Sci, I-95126 Catania, Italy
[2] Univ Catania, Res Ctr Extreme Senescence, Dept Aging Sci, I-95126 Catania, Italy
[3] Univ Catania, Dept Surg Policlin Gaspare Rodol, I-95123 Catania, Italy
关键词:
Pancreatic cancer;
Neuroendocrine components;
Chromogranin A;
Carbohydrate antigen (CA19-9);
SOMATOSTATIN RECEPTORS;
PROGNOSTIC VALUE;
CA-19-9;
LEVELS;
CATECHOLAMINE;
EXPRESSION;
ENDOCRINE;
CARCINOMA;
RELEASE;
DISEASE;
TUMORS;
D O I:
10.1016/j.archger.2008.01.014
中图分类号:
R592 [老年病学];
C [社会科学总论];
学科分类号:
03 ;
0303 ;
100203 ;
摘要:
The neuroendocrine differentiation in PC could potentially represent a new finding with diagnostic, prognostic and therapeutic implications. This study aimed at evaluating the clinical usefulness of CgA as a neuroendocrine (NE) serum-marker. We investigated the role of the serum concentration of CgA in a study group of patients with PC. CgA was significantly higher in the patients affected by PC as compared with the group of healthy subjects (HS) and those with chronic pancreatitis (CHP) (p < 0.001). Also the HS group differed significantly from the CHP control group in the serum CgA levels (p < 0.001). The serum carbohydrate antigen (CA19-9) level displayed a significant difference (p < 0.001) between the PC and the HS group. The PC and CHP groups, as well as the HS and CHP groups showed also significant differences in the CA19-9 levels (p < 0.001). One can conclude that the patients with higher CgA levels had poorer prognosis and survival, as compared to those with lower CgA levels. These results support the notion that the determination of serum CgA level before treatment may be a potential prognostic factor for PC. (C) 2008 Elsevier Ireland Ltd. All rights reserved.
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页码:213 / 217
页数:5
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