Thick cutaneous malignant melanoma: a reappraisal of prognostic factors

Citation
D. Massi et al., Thick cutaneous malignant melanoma: a reappraisal of prognostic factors, MELANOMA RE, 10(2), 2000, pp. 153-164
Citations number
37
Categorie Soggetti
Oncology,"Onconogenesis & Cancer Research
Journal title
MELANOMA RESEARCH
ISSN journal
09608931 → ACNP
Volume
10
Issue
2
Year of publication
2000
Pages
153 - 164
Database
ISI
SICI code
0960-8931(200004)10:2<153:TCMMAR>2.0.ZU;2-3
Abstract
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.