BIOLOGIC AND CLINICAL CORRELATIONS AMONG PLOIDY, CELL-KINETICS, AND THE TUMOR-ASSOCIATED GLYCOPROTEIN-72 TISSUE EXPRESSION IN COLORECTAL-CANCER - PRELIMINARY FINDINGS
F. Cavaliere et al., BIOLOGIC AND CLINICAL CORRELATIONS AMONG PLOIDY, CELL-KINETICS, AND THE TUMOR-ASSOCIATED GLYCOPROTEIN-72 TISSUE EXPRESSION IN COLORECTAL-CANCER - PRELIMINARY FINDINGS, Diseases of the colon & rectum, 37(2), 1994, pp. 190000024-190000029
PURPOSE: The aim of this study was to evaluate the possibility of iden
tifying biologically aggressive subgroups of patients, combining sever
al biologic parameters such as the tumor and normal mucosa values from
the ploidy, the S-phase cell percentage, and tumor-associated glycopr
otein-72 (TAG-72) expression. METHODS: One hundred five colorectal can
cer patients were studied to analyze the possible prognostic role of p
loidy and cell kinetics in multiple fresh specimens from the tumor and
normal mucosa. Since the presence of TAG-72 in the colonic mucosa has
been correlated to neoplastic transformation, the correlations betwee
n these parameters and the quantitative tissue expression of the TAG-7
2 were analyzed in a subgroup of 53 cases. RESULTS: A significantly lo
wer five-year disease-free survival rate (21.4 percent) was observed i
n patients with multiploid tumors, when compared with that observed in
patients with diploid or single aneuploid tumors (67.5 percent) (P =
0.03). The quantitative tissue TAG-72 expression contributed in identi
fying a particular patient subgroup (20 percent), characterized by S-p
hase percentage and TAG-72 values from the normal mucosa that were une
xpectedly higher than 12.1 percent and 7.5 U/mg of proteins, respectiv
ely. In particular, when the 25 Dukes B patients were analyzed, simila
r results were observed. In fact, 14 (56 percent) cases showed high tu
mor cell proliferation and, surprisingly, a high tissue TAG-72 content
in the normal mucosa was found in 4 (28.6 percent) of these patients.
CONCLUSIONS: Other than multiploidy, the biologic aggressiveness of c
olorectal cancer might be successfully assessed introducing the evalua
tion of new biologic parameters, such as the TAG-72 content and S-phas
e percentage values of the normal mucosa, suggesting the possibility o
f further stratifying this patient population.