T. Vogt et al., P53-PROTEIN AND KI-67-ANTIGEN EXPRESSION ARE BOTH RELIABLE BIOMARKERSOF PROGNOSIS IN THICK STAGE-I NODULAR MELANOMAS OF THE SKIN, Histopathology, 30(1), 1997, pp. 57-63
The maximum tumour thickness is the most important prognostic factor i
n malignant melanomas of the skin. However, the clinical outcome of th
ick nodular melanomas remains unpredictable. Therefore, we investigate
d possible prognostic markers in this subset of melanomas. From a mela
noma data base, 12 patients with thick ( >3 mm) stage I nodular melano
mas of the skin were identified, who were still without signs of progr
ession after five years of follow-up. These tumours were compared to a
randomly selected series of 12 cases, who did not survive the first f
ive years after removal of the tumours. We performed immunostaining fo
r the p53-protein and the proliferation associated Ki-67-antigen. For
quantification of immunostaining the tumours were entirely scanned. In
addition, all tumours were investigated for any differences with conv
entionally applied prognostic features: the tumour thickness; the leve
l of invasion; the prognostic index (tumour thickness multiplied by mi
totic count): and the mean volume-weighted mean nuclear volume. We dem
onstrated significant differences between survivors and non-survivors
exclusively in respect of the staining-indices for p53 and Ki-67 (P <0
.03 and 0.02, respectively). With both antibodies the tumours of survi
vors showed lower counts as compared to nonsurvivors. However, within
both groups we found no significant correlations between the p53- and
Ki-67-staining results. We conclude that immunostaining for p53-protei
n and Ki-67-antigen is helpful to identify individuals with thick nodu
lar melanomas who are at risk of metastatic disease.