DNA ploidy has been shown to be a predictive parameter for prognosis in var
ious solid tumours. The prognostic value of DNA-ploidy in gastric cancers i
s still a matter of controversy. A possible explanation for the discrepant
results reported in the literature could be sampling error in tumours with
multiple stemlines differing in DNA-ploidy.
In order to determine whether or not such heterogeneity exists in early gas
tric carcinoma, we have performed DNA cytophotometry on multiple samples of
a group of 17 early gastric carcinomas, of which 8 were pure intramucosal
and 9 were infiltrating into the submucosa.
We found an aneuploid DNA-stemline in 8 (47%) early gastric cancers, more o
ften in tumours invading into the submucosa (5/9) than in purely mucosal ru
mours (3/8). Multiple DNA-stemlines were found more frequently in submucosa
lly infiltrating rumours (4/5).
These results confirm the presence of DNA-aneuploid early gastric carcinoma
which are frequently heterogeneous and suggest that heterogeneity occurs m
ore frequently in tumours invading the submucosa. This heterogeneity is bes
t detected by analysing multiple samples of tumours for DNA-ploidy.