Gastrin-releasing-peptide (GRP) the mammalian counterpart of amphibian bomb
esin, has been reported to be produced by cells of SCLC. Using recombinant
ProGRP Yamaguchi et al developed an enzyme immunoassay for the measurement
of this more stable precursor of GRP. We focused our interest on the compar
ability of ProGRP to neuron specific enolase (NSE) CYFRA 21-1 and CEA. For
this purpose we investigated the sera of 272 patients with histologically p
roven carcinomas of the lung (87 SCLC, 185 NSCLC). The sera of 74 patients
with benign diseases of the lung and smokers sewed as a reference group. At
a specificity of 95% ProGRP and NSE possessed comparable sensitivities (47
% versus 45%) in small cell lung carcinomas. ProGRP showed only a few more
positive test results than NSE, but reached much higher value levels than N
SE. ProGRP and NSE showed a clear additive sensitivity of about 20 %. In NS
CLC CYFRA 21-1 was the leading marker with 63 % sensitivity whereas ProGRP
seldom showed a "false positive" test result. ProGRP proved a very high spe
cificity and good sensitivity for small cell lung carcinomas and therefore
enables diagnosis of small cell lung carcinoma in patients with lung tumour
s of unknown origin as well as good control of efficiency of therapy.