G. Scambia et al., NM23 IN OVARIAN-CANCER - CORRELATION WITH CLINICAL OUTCOME AND OTHER CLINICOPATHOLOGICAL AND BIOCHEMICAL PROGNOSTIC PARAMETERS, Journal of clinical oncology, 14(2), 1996, pp. 334-342
Purpose: The aim of the study was to define the prognostic role of the
metastasis suppressor gene, nm23, in 106 primary ovarian cancer patie
nts. Patients and Methods: Northern and Western blotting analysis of n
m23-H1 and nm23-H2 expression were performed in a subset of ovarian tu
mors. Immunohistochemical analysis was performed on formalin-fixed par
affin-embedded specimens from 106 primary ovarian carcinomas by the an
tihuman nm23 monoclonal antibody. Results: Northern and Western blotti
ng analysis demonstrated a direct association between nm23-H1 and nm23
-H2 levels. Moreover, an overall concordance of 86.7% between Northern
blotting and immunohistochemical data was observed. Sixty-six specime
ns (68%) showed a positive nm23-H1 immunoreaction. The percentage of n
m23-H1 positivity was higher in lymph nodenegative (70%) than in lymph
node-positive cases (44%) (P=.049). Moreover, the percentage of compl
ete/partial responses to chemotherapy wets higher in nm23-H1-positive
(69%) than in nm23-H1-negative (44%) patients (P=.03). The percentage
of epidermal growth factor receptor (EGFR) positive cases was lower in
nm23-H1-positive (44%) than in nm23-H1-negative immunostained (72%) s
amples (P=.012). Lower ras/p21 levels (median, 1.77 absorbance units)
were found in nm23-H1-positive than in nm23-H1-negative samples (media
n, 2.63 absorbance units) (P=.03), The 6-year progression-free surviva
l (PFS) rate of nm23-H1-positive cases was 50% (95% confidence interva
l [CI], 33 to 67) versus 12% (95% CI, -2 to 26) for nm23-H1-negative p
atients (P=.0056). In multivariate analysis, only stage, ascites, and
nm23-H1 content retained independent prognostic roles. Conclusion: The
assessment of nm23 content may provide useful information for prognos
tic characterization of ovarian cancer patients. (C) 1996 by American
Society of Clinical Oncology.