The prognosis of patients with thick (>3 mm) cutaneous malignant melanomas
is generally poor; however, some cases survive far longer than expected. Th
us tumour thickness cannot serve as the only predictor of disease course in
the individual patient. The aims of the current study were to evaluate the
clinical outcome of patients with thick (> 3 mm) cutaneous melanoma and te
st the prognostic value of a series of clinicopathological parameters on di
sease-free and cause-specific survival. We retrospectively evaluated 140 pa
tients with stage I cutaneous melanoma > 3 mm in thickness. Disease-free an
d cause-specific survival rates (Kaplan Meier method) were compared using t
he log rank test. A multivariate analysis (Cox proportional hazards model)
was used to determine the independent effect of each variable on prognosis.
The overall 5-year and 10-year disease-free survival rates were 35.5% and
29.3%, respectively, whereas the overall 5-year and 10-year cause-specific
survival rates were 55.3% and 47.7%, respectively. In the univariate analys
is, the following factors were found to be significantly associated with th
e disease-free and cause-specific survival: tumour thickness, mitotic rate/
mm(2), type of invasive front, ulceration, thickness of the nodular compone
nt and predominant cell type. In addition, the presence of vascular invasio
n was significantly correlated with the risk of metastases but not with sur
vival. In the multivariate analysis (Cox proportional hazards model), only
tumour thickness (both as a continuous variable and > 7.5 mm), infiltrating
invasive front, presence of ulceration and mitotic rate/mm(2) (both as a c
ontinuous variable and > 10 mitoses/mm(2)) were significant independent pre
dictors of poorer clinical outcome. (C) 2000 Lippincott Williams & Wilkins.