C. Charpin et al., CD31 PECAM AUTOMATED AND QUANTITATIVE IMMUNOCYTOCHEMICAL ASSAYS IN BREAST CARCINOMAS - CORRELATION WITH PATIENT FOLLOW-UP/, American journal of clinical pathology, 107(5), 1997, pp. 534-541
The purpose of this study was to determine the prognostic significance
of quantitative CD31 immunohistochemical assays. CD31 assays were per
formed on a series of 167 breast carcinoma specimens under optimal tec
hnical conditions that involved frozen sections, an automated immunope
roxidase technique, and computer-assisted analysis of digitized colore
d microscopic images. Results of automated quantitative immunohistoche
mical assays were correlated with patient follow-up (9.6 years). Patie
nts were divided into two subgroups: those who had axillary lymph node
-positive (N+) disease and those who had lymph node-negative (N-) dise
ase. The marked immunocytochemical expression of CD31 in tumors (cutof
f point, 20%) was significantly (P = .033) associated with a poor over
all survival rate (Kaplan-Meier, log rank test); however, a significan
t association was not observed in the N+ and N- subgroups. CD31-immuno
stained tumor cell surfaces larger than 20% correlated with the metast
asis-free survival rate (P = .004) in air patients and in the N+ subgr
oup (P = .005) but not in the N- subgroup. In addition, marked immunoc
ytochemical expression of CD31 correlated with the short-term disease-
free survival rate (P = .04) in the N+ subgroup but not in the N- subg
roup. in multivariate analysis (proportional hazards regression Cox mo
del) the prognostic significance of CD31 was independent of tumor size
and histologic type but not of grade. The results suggest that, under
optimal technical conditions (automated and quantitative immunohistoc
hemical assays on frozen sections), immunohistochemical expression of
CD31 is a significant prognostic indicator of overall and metastasis-f
ree survival rates. CD31 has limited prognostic value, however, and is
not a completely independent prognostic indicator because it is relat
ed to nodal status.