Diagnostic value of chromogranin A in pancreatic neuroendocrine tumors depends on tumor size: A prospective observational study from a single institute

被引:18
|
作者
Jun, Eunsung [1 ,2 ]
Kim, Song Cheol [2 ,4 ]
Song, Ki Byung [2 ]
Hwang, Dae Wook [2 ]
Lee, Jae Hoon [2 ]
Shin, Sang Hyun [2 ]
Hong, Seung Mo [3 ]
Park, Kwang-Min [2 ]
Lee, Young-Joo [2 ]
机构
[1] Univ Ulsan, Coll Med, Dept Biomed Sci, Seoul, South Korea
[2] Univ Ulsan, Coll Med, Dept Surg, Div Hepatobiliary & Pancreat Surg, Seoul, South Korea
[3] Univ Ulsan, Coll Med, Dept Pathol, Seoul, South Korea
[4] Asan Med Ctr, 388-1 Pungnap 2 Dong, Seoul 138736, South Korea
关键词
NEURON-SPECIFIC ENOLASE; FINE-NEEDLE-ASPIRATION; BIOLOGICAL FUNCTION; PROSTATE-CANCER; USEFUL MARKER; SERUM; MANAGEMENT; DIFFERENTIATION; EXPRESSION; BREAST;
D O I
10.1016/j.surg.2017.01.019
中图分类号
R61 [外科手术学];
学科分类号
摘要
Background. Chromogranin A has recently been recommended as the most practical tumor marker in patients with pancreatic neuroendocrine tumors. However, the diagnostic effectiveness of circulating chromogranin A levels remains controversial. Here, we aimed to assess the clinical diagnostic value of plasma chromogranin A levels for pancreatic neuroendocrine tumors. Methods. Between June 2012 and June 2015, 110 consecutive patients with a suspected pancreatic neuroendocrine tumor were prospectively enrolled. We evaluated the diagnostic value of the. chromogranin A assay for differentiating pancreatic neuroendocrine tumors from other tumors. The plasma chromogranin A levels in the pancreatic neuroendocrine tumor patients were examined according to various clinicopathologic factors. Results. A total of 65 patients were diagnosed as having pancreatic neuroendocrine tumors, whereas 45 had other tumors. The median chromogranin A level in pancreatic neuroendocrine tumor cases was higher than that in cases of other tumors (pancreatic neuroendocrine tumors: 126.62 ng/mL, other tumors: 69.82 ng/mL). The sensitivity, specificity, and accuracy of the chromogranin A assay for pancreatic neuroendocrine tumor diagnosis were 49.2%, 77.8%, and 60.9%, respectively. The chromogranin A levels after operative resection were reduced or were confirmed as being within the normal range (78.9%) in most cases. Moreover, the chromogranin A level in pancreatic neuroendocrine tumors cases was correlated with tumor size based on comparisons with other tumors in the pancreas (P = .038). The sensitivity, specificity, and accuracy of the chromogranin A assay for large tumors were greater, at 64.3 %, 100.0%, and 81.5 %, respectively. Conclusion. In clinical settings, the identification of pancreatic neuroendocrine tumors is vital for the development of therapeutic strategies. In large pancreatic tumors, the measurement of chromogranin A levels is very useful for distinguishing pancreatic neuroendocrine tumors from other tumors in the pancreas.
引用
收藏
页码:120 / 130
页数:11
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