黑色素瘤
医学
肢端皮损性黑色素瘤
比例危险模型
布雷斯洛厚度
生存分析
危险系数
皮肤病科
内科学
对数秩检验
肿瘤科
单变量分析
癌症
多元分析
置信区间
癌症研究
乳腺癌
前哨淋巴结
作者
Giovanni Paolino,Bekkenk Mw,Dario Didona,Laura Eibenschutz,Richetta Ag,Carmen Cantisani,G Viti,Anna Carbone,Pierluigi Buccini,Paola De Simone,Angela Ferrari,Elisabetta Scali,Stefano Calvieri,Vitaliano Silipo,Emanuele Cigna,Viti Gp,Ugo Bottoni
出处
期刊:PubMed
日期:2016-03-01
卷期号:20 (5): 842-8
被引量:17
摘要
Acral melanoma is an uncommon type of melanoma in Caucasian patients. However, acral melanoma is the most common type of melanoma in African and Asian patients. Comparison analyses between hand-acral melanoma and foot-acral melanoma have been rarely reported in the literature. Acral melanoma is an uncommon melanocytic tumor characterized by an intrinsic aggressiveness, with specific histological and clinicopathological features. Acral melanoma involves the palms, soles and sub-ungueal sites.A total of 244 patients with acral melanoma were included in our analysis. The current study was performed in three different medical centers: Sapienza University of Rome, San Gallicano Institute of Rome and University of Magna Graecia (Italy). The Kaplan-Meier product was used to estimate survival curves for disease-free survival and overall survival. The log-rank test was used to evaluate differences between the survival curves. Assuming that the effects of the predictor variables are constant over time, the independent predictive factors were assessed by Spearman's test and subsequently data were analyzed performing Cox proportional-hazard regression.In both univariate and multivariate analyses Breslow thickness (p < 0.0001) and ulceration (p = 0.003) remained the main predictors. General BRAF mutation was detected in 13.8% of cases. We found that median Breslow value and the percentage of recurrences were similar in hand-acral melanoma and foot-acral melanoma, as well as there were no differences in both short and long-term.The absence of differences in survival between hand-acral melanoma and foot-acral melanoma shows that the aggressiveness of the disease is related to distinct mutational rate, as well as to anatomical site-specific features, rather than to the visibility of the primary lesion.
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