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. 2017:2017:2467870.
doi: 10.1155/2017/2467870. Epub 2017 Feb 19.

Diagnostic Value of CYFRA 21-1 in the Cerebrospinal Fluid for Leptomeningeal Metastasis

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Diagnostic Value of CYFRA 21-1 in the Cerebrospinal Fluid for Leptomeningeal Metastasis

Zhen Zhang et al. Dis Markers. 2017.

Abstract

Cerebrospinal fluid (CSF) cytology has low sensitivity for leptomeningeal metastasis (LM); thus, new markers are needed to improve the diagnostic accuracy of LM. We measured carcinoembryonic antigen (CEA) and cytokeratin 19 fragments (CYFRA 21-1) in paired samples of CSF and serum from patients with LM and patients with nonmalignant neurological diseases (NMNDs) as controls. Receiver operating curve analysis was performed to assess their diagnostic accuracy for LM. In patients with NMNDs, CEA and CYFRA 21-1 levels in the CSF were significantly lower than the serum levels. In patients with LM, there was no significant difference between the CSF and serum CEA levels, whereas the CYFRA 21-1 levels were significantly higher in the CSF than the serum. CSF/serum quotients of CYFRA 21-1 were higher than those of CEA in patients with LM and patients with NMNDs. CSF CYFRA 21-1 and CSF/serum quotient of CYFRA 21-1 had high accuracy for differentiating LM from NMNDs that was similar to CSF CEA and CSF/serum quotient of CYFRA 21-1, whereas serum CYFRA 21-1 is of poor diagnostic value. Measurement of CSF CYFRA 21-1 should not be overlooked in patients with suspected LM, even if the serum CYFRA 21-1 level is within normal limits.

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Conflict of interest statement

There is no conflict of interests to be disclosed.

Figures

Figure 1
Figure 1
Receiver operating characteristic curves of cerebrospinal fluid (CSF) carcinoembryonic antigen (CEA), serum CEA, and CSF/serum quotient of CEA for differentiating between leptomeningeal metastasis and nonmalignant neurological diseases.
Figure 2
Figure 2
Receiver operating characteristic curves of cerebrospinal fluid (CSF) CYFRA 21-1, serum CYFRA 21-1, and CSF/serum quotient of CYFRA 21-1 for differentiating between leptomeningeal metastasis and nonmalignant neurological diseases.

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