Iol. Ng et al., CEA TISSUE-STAINING IN COLORECTAL-CANCER PATIENTS - CORRELATION WITH PLASMA CEA, HISTOLOGY AND STAGING, Pathology, 25(3), 1993, pp. 219-222
To study the expression of tissue carcinoembryonic antigen (CEA) by im
munoperoxidase staining in colorectal adenocarcinomas and its relation
with preoperative serum CEA and clinicopathological parameters, we st
udied 85 unselected patients who underwent resective surgery for color
ectal adenocarcinomas and were followed up for a mean of 66 mths. All
tumors except 2 showed positive staining for CEA. The staining pattern
was classifiable into 4 types: apical, cytoplasmic, basolateral and s
tromal, according to the predominant sites of staining. We found a sig
nificant positive correlation between tissue CEA staining pattern and
preoperative plasma CEA. Plasma CEA levels were higher when tumor cell
staining extended to basolateral regions of the cells and into stroma
l tissues rather than restricted to apical and cytoplasmic regions (p
= 0.012). Furthermore, tissue CEA staining also correlated positively
with vascular invasion by tumor cells (p = 0.046), with basolateral an
d stromal types associated with more frequent vascular invasion than a
pical and cytoplasmic types. This was in contrast to the preoperative
CEA which did not correlate with vascular permeation. We speculate tha
t tissue CEA staining is useful in indicating possible vascular invasi
on even at early stage whereas vascular invasion by a larger tumor bul
k or even tumor metastases may be necessary to produce an increased pl
asma CEA level that is detectable. On the other hand, preoperative pla
sma CEA had a strong, positive relationship with tumor stage and morta
lity (p < 0.001 for both). Preoperative CEA was higher in tumors showi
ng moderate and poor differentiation, although it did not reach statis
tical significance (p = 0.068), whereas tissue CEA staining had no cor
relation with tumor differention. Although tissue CEA staining pattern
s appear useful in explaining some pathophysiological events, it offer
s little additional information to plasma CEA in management of patient
s with colorectal carcinoma.