P. Bertheau et al., C-ERBB-2, P53, AND NM23 GENE-PRODUCT EXPRESSION IN BREAST-CANCER IN YOUNG-WOMEN - IMMUNOHISTOCHEMICAL ANALYSIS AND CLINICOPATHOLOGICAL CORRELATION, Human pathology, 29(4), 1998, pp. 323-329
We studied c-erbB-2, p53, and nm23 gene products in 112 primary breast
carcinomas. Fifty patients were aged 35 years or younger, and 62 were
aged 36 to 50. Clinicopathological criteria including clinical stage,
hormone receptor status, histological types, histological grades, and
lymph node status, were reviewed. Disease-free survival (DFS) and ove
rall survival (OS) were analyzed. Immunohistochemical findings were as
sessed semiquantitatively. Correlation between clinicopathological cri
teria, survival data, and immunohistochemical findings have been made.
Patients aged younger than 35 years with stage I to II disease had a
shorter DFS (P=.03) than older patients. However, no other clinicopath
ological finding was associated with age. Neither was there associatio
n between age and c-erbB-2, p53, or nm23 patterns of expression. p53 p
ositivity was associated with high histological grade (P =.003) and wi
th progesterone receptor negativity (P=.045). Nm23 nuclear positivity
was associated with early clinical stages (P =.011) and with absence o
f axillary lymph node metastasis (P=.007). p53 and c-erbB-2 overexpres
sion were associated with shorter OS while nm23 nuclear positivity was
associated with longer OS in univariate and multivariate analyses. Un
ivariate analyses showed that c-erbB-2 or nm23 were potentially import
ant prognostic factors in women aged 35 years or younger while p53 was
associated with prognosis in women aged 36 to 50. Cox model analysis
indicated that c-erbB-2 alone was associated with prognosis in women 3
5 years and younger, whereas p53 alone was associated with prognosis i
n 36- to 50-year-old women. These results suggest that breast cancer i
n the youngest women has some biological specificity. Copyright (C) 19
98 by W.B. Saunders Company.