THE COMBINATION OF A DECISION TREE TECHNIQUE WITH THE COMPUTER-ASSISTED MICROSCOPE ANALYSIS OF FEULGEN-STAINED NUCLEI TO ASSESS AGGRESSIVENESS IN LIPOMATOUS AND SMOOTH-MUSCLE TUMORS
C. Decaestecker et al., THE COMBINATION OF A DECISION TREE TECHNIQUE WITH THE COMPUTER-ASSISTED MICROSCOPE ANALYSIS OF FEULGEN-STAINED NUCLEI TO ASSESS AGGRESSIVENESS IN LIPOMATOUS AND SMOOTH-MUSCLE TUMORS, Anticancer research, 15(4), 1995, pp. 1311-1317
The present study describes a computer-assisted methodology whose purp
ose is to I educe the degree of subjectivity in the diagnosis of soft
tissue tumors. This methodology associates three complementary techniq
ues, namely digital cell image analysis, the discretisation of numeric
al data and a Decision TI ee technique (DT). The first technique relie
s on the use of the digital cell image analysis of Feulgen-stained nuc
lei, a technique which makes possible a quantitative and thus objectiv
e description of nuclei with the help of 24 numerical parameters (15 m
olphonuclear and 9 DNA content- (ploidy level and proliferation activi
ty) related). The second technique transforms each numerical parameter
into an ordinal one with a small number of values (2 to 4) so that on
ly the relevant physical significance of the parameters is retained Th
e Decision Tree technique generates classification rules on the basis
of the discretised parameters quoted above. This methodology was appli
ed to 53 human soft tissue tumors which included 26 lipomatous tumors
(13 malignant liposarcomas and 13 benign lipomas) and 27 smooth muscle
tumors (11 malignant leiomyosarcomas and 16 benign leiomyomas). The r
esults show that a distinction between benign (lipoma) and malignant (
liposarcoma) lipomatous tumors can easily be made by means of simple l
ogical rules depending on only foul discretised cytological parameters
(two ploidy- and two morphonuclear-related). In contrast, no stable o
r predictive characterisation can be obtained with respect to the diff
erence between leiomyosarcomas and the leiomyomas. Hence, while lipoma
s and liposarcomas appeared to be two completely distinct biological e
ntities, leiomyomas and leiomyosarcomas seem to involve a continuous b
iological process.