Diagnostic utility of CYFRA 21-1, carcinoembryonic antigen, CA 125, neuronspecific enolase, and squamous cell antigen level determinations in the serum and pleural fluid of patients with pleural effusions
J. Ferrer et al., Diagnostic utility of CYFRA 21-1, carcinoembryonic antigen, CA 125, neuronspecific enolase, and squamous cell antigen level determinations in the serum and pleural fluid of patients with pleural effusions, CANCER, 86(8), 1999, pp. 1488-1495
BACKGROUND. To the authors' knowledge the role of tumor marker determinatio
n in the differential diagnosis of pleural effusions has not been establish
ed definitively. The current article reports the results of a study of CYFR
A 21-1, carcinoembryonic antigen (CEA), cancer antigen 125 (CA 125), squamo
us cell antigen (SCC), and neuron specific enolase (NSE) in the serum and p
leural fluid of patients with pleural effusions of diverse etiologies.
METHODS. One hundred forty-six patients with pleural effusions [43 malignan
t, 47 tuberculous, 32 miscellaneous benign, and 24 paramalignant) were stud
ied prospectively. Levels of CYFRA 21-1, CA 125, CEA, NSE, and SCC were mea
sured by radioimmunoassay in the pleural fluid in all patients and in the s
erum in 118 patients.
RESULTS. There were no significant differences between the serum and pleura
l fluid levels of tumor markers with the exception of CA 125, which was hig
her in the pleural fluid. With maximum specificity, the highest sensitivity
in the diagnosis of pleural malignancy was obtained with a combination of
CYFRA 21-1 with a cutoff value of 150 U/L), CEA (with a cutoff value of 40
ng/mL), and CA 125 with a cutoff value of 1000 ng/mL) in pleural fluid. NSE
and SCC added no diagnostic value. The simultaneous use of tumor markers a
nd cytology in pleural fluid increased the sensitivity from 55.8% to 81%.
CONCLUSIONS. These findings suggest that a combination of CYFRA 21-1, CEA,
and CA 125 in the pleural fluid can be a useful addition to pleural cytolog
y in the diagnosis of malignant pleural effusion. (C) 1999 American Cancer
Society.