Soluble interleukin-2 receptor, intercellular adhesion molecule-1 and interleukin-10 serum levels in patients with melanoma

被引:69
作者
Boyano, MD [1 ]
Garcia-Vázquez, MD
López-Michelena, T
Gardeazabal, J
Bilbao, J
Cañavate, ML
De Galdeano, AG
Izu, R
Díaz-Ramón, L
Raton, JA
Díaz-Pérez, JL
机构
[1] Univ Basque Country, Sch Med & Dent, Dept Cell Biol & Morphol Sci, Leioa 48940, Bizkaia, Spain
[2] Cruces Hosp, Dept Dermatol, Baracaldo 48903, Bizkaia, Spain
[3] Univ Basque Country, Sch Med & Dent, Dept Prevent Med & Publ Hlth, Leioa 48940, Bizkaia, Spain
关键词
sIL-2R; sICAM-1; IL-10; biological prognostic factors; melanoma progression;
D O I
10.1054/bjoc.2000.1402
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Serum soluble interleukin-2 receptor (sIL-2R), intercellular adhesion molecule-1 (sICAM-1) and interleukin-10 (IL-10) have each been reported as useful markers for melanoma progression. To evaluate the clinical relevance of these three markers, we simultaneously analysed their serum levels in patients with melanoma. A longitudinal study with a 3-year follow-up was performed and different stages of the disease were considered. Mean values of sIL-2R were significantly higher than in normal controls in all stages and correlated with the disease progression. The prognosis of patients with levels > 529 U/ml of sIL-2R was significantly poorer than in patients with sIL-2R levels < 529 U/ml. Levels of sICAM-1 were also elevated in melanoma patients, specially at the time of the metastatic disease. Serum IL-10 levels were more frequently detectable in the patients that developed metastasis during follow-up, and the prognosis of patients with detectable IL-10 levels was significantly poorer than in those patients with IL-10 undetected levels. Statistical analysis based on Logistic and Cox regression models showed that only sex, stage and sIL-2R value are factors significantly associated with metastatic progression. Moreover, high levels of sIL-2R could be a risk factor for malignant progression in melanoma. (C) 2000 Cancer Research Campaign.
引用
收藏
页码:847 / 852
页数:6
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