Approximately 20% of pleural effusions are caused by neoplastic proces
ses. Although cytology is the most specific routine diagnostic procedu
re: its sensitivity of 50-60% is insufficient, and thus diagnosis is u
sually carried out by more invasive techniques such as pleural biopsy,
thoracoscopy or thoracotomy. The object of this study is to evaluate
the use of determining some tumour markers in pleural fluid obtained b
y thoracocentesis for diagnosis of neoplastic pleural effusion. Patien
ts (271) with pleural effusions were classified in five groups: I: neo
plasms n = 88; II: tuberculosis n = 63; III: parapneumonics n = 53; TV
: miscellaneous exudates n = 39 and V: transudates n = 28. The tumour
markers studied were: carcinoembryonic antigen (CEA), CA 125, squamous
cell carcinoma antigen (SCC), and neuron specific enolase (NSE). The
tumour makers had the following diagnostic efficiencies for neoplastic
origin of the pleural effusion: CEA 76% (sensitivity 31%, specificity
93%); CA 125 66% (70% and 61%); SCC 65% (48% and 80%) and NSE 53% (30
% and 89%). The diagnostic efficiencies for pulmonary neoplastic origi
ns were 68% for NSE (sensitivity 83%, specificity 53%); 65% for SCC (5
4% and 75%); 63% for CEA (80% and 48%) and 61% for CA 125 (79% and 42%
). We believe that the routine testing of tumour markers in pleural fl
uid obtained by thoracocentesis would greatly increase diagnostic effe
ctiveness and could avoid the practice of more aggressive diagnostic t
echniques on the patient. (C) 1997 Elsevier Science B.V.