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Serum markers in early-stage and locally advanced melanoma

The identification of prognostic factors in cutaneous melanoma allows choosing the most effective treatment, especially in group of patients with locoregional disease. Markers related to carcinogenesis and angiogenesis in particular have effect on the course of the disease. The aim of this study was...

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Autores principales: Lugowska, Iwona, Kowalska, Maria, Fuksiewicz, Małgorzata, Kotowicz, Beata, Mierzejewska, Ewa, Koseła-Paterczyk, Hanna, Szamotulska, Katarzyna, Rutkowski, Piotr
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Netherlands 2015
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4672018/
https://www.ncbi.nlm.nih.gov/pubmed/26002577
http://dx.doi.org/10.1007/s13277-015-3564-2
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author Lugowska, Iwona
Kowalska, Maria
Fuksiewicz, Małgorzata
Kotowicz, Beata
Mierzejewska, Ewa
Koseła-Paterczyk, Hanna
Szamotulska, Katarzyna
Rutkowski, Piotr
author_facet Lugowska, Iwona
Kowalska, Maria
Fuksiewicz, Małgorzata
Kotowicz, Beata
Mierzejewska, Ewa
Koseła-Paterczyk, Hanna
Szamotulska, Katarzyna
Rutkowski, Piotr
author_sort Lugowska, Iwona
collection PubMed
description The identification of prognostic factors in cutaneous melanoma allows choosing the most effective treatment, especially in group of patients with locoregional disease. Markers related to carcinogenesis and angiogenesis in particular have effect on the course of the disease. The aim of this study was to evaluate clinical utility of vascular endothelial growth factor (VEGF), matrix metalloproteinase 2 (MMP-2), MMP-9, tissue inhibitors of metalloproteinase 1 (TIMP-1), and YKL-40 in serum of melanoma patients at pathological stages I–III. We included 148 adult patients with melanoma. The median follow-up was 40 months. Disease recurrence was observed in 43 patients; 3-year disease-free survival (DFS) rate was 71.7 %; 35 patients died; and the 3-year overall survival (OS) rate was 85 %. Concentrations of VEGF, MMP-2, MMP-9, TIMP-1, and YKL-40 were measured by ELISA kits. VEGF, MMP-9, TIMP-1, and YKL-40 were significantly higher in group of patients than in controls. Increased concentrations of TIMP-1 were related to patient survival, which in the group of lower and increased TIMP-1, disease-free survival amounted to 81 vs. 61 % (p = 0.014) and overall survival −88 vs. 82 % (p = 0.050), respectively. An increased concentration of YKL-40 was observed in 59 % of patients with ulceration and in 26 % of patients without ulceration (p = 0.012). We have found a clinically significant correlation between YKL-40 and MMP-9 (rho = 0.363; p = 0.004) as well as YKL-40 and VEGF (rho = 0.306; p = 0.018). In melanoma patients at stages I–III, the high concentrations of TIMP-1 in serum predicted adverse prognosis. YKL-40 was associated with ulceration of primary tumor, which is a very important prognostic factor.
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spelling pubmed-46720182015-12-16 Serum markers in early-stage and locally advanced melanoma Lugowska, Iwona Kowalska, Maria Fuksiewicz, Małgorzata Kotowicz, Beata Mierzejewska, Ewa Koseła-Paterczyk, Hanna Szamotulska, Katarzyna Rutkowski, Piotr Tumour Biol Research Article The identification of prognostic factors in cutaneous melanoma allows choosing the most effective treatment, especially in group of patients with locoregional disease. Markers related to carcinogenesis and angiogenesis in particular have effect on the course of the disease. The aim of this study was to evaluate clinical utility of vascular endothelial growth factor (VEGF), matrix metalloproteinase 2 (MMP-2), MMP-9, tissue inhibitors of metalloproteinase 1 (TIMP-1), and YKL-40 in serum of melanoma patients at pathological stages I–III. We included 148 adult patients with melanoma. The median follow-up was 40 months. Disease recurrence was observed in 43 patients; 3-year disease-free survival (DFS) rate was 71.7 %; 35 patients died; and the 3-year overall survival (OS) rate was 85 %. Concentrations of VEGF, MMP-2, MMP-9, TIMP-1, and YKL-40 were measured by ELISA kits. VEGF, MMP-9, TIMP-1, and YKL-40 were significantly higher in group of patients than in controls. Increased concentrations of TIMP-1 were related to patient survival, which in the group of lower and increased TIMP-1, disease-free survival amounted to 81 vs. 61 % (p = 0.014) and overall survival −88 vs. 82 % (p = 0.050), respectively. An increased concentration of YKL-40 was observed in 59 % of patients with ulceration and in 26 % of patients without ulceration (p = 0.012). We have found a clinically significant correlation between YKL-40 and MMP-9 (rho = 0.363; p = 0.004) as well as YKL-40 and VEGF (rho = 0.306; p = 0.018). In melanoma patients at stages I–III, the high concentrations of TIMP-1 in serum predicted adverse prognosis. YKL-40 was associated with ulceration of primary tumor, which is a very important prognostic factor. Springer Netherlands 2015-05-23 /pmc/articles/PMC4672018/ /pubmed/26002577 http://dx.doi.org/10.1007/s13277-015-3564-2 Text en © The Author(s) 2015 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Research Article
Lugowska, Iwona
Kowalska, Maria
Fuksiewicz, Małgorzata
Kotowicz, Beata
Mierzejewska, Ewa
Koseła-Paterczyk, Hanna
Szamotulska, Katarzyna
Rutkowski, Piotr
Serum markers in early-stage and locally advanced melanoma
title Serum markers in early-stage and locally advanced melanoma
title_full Serum markers in early-stage and locally advanced melanoma
title_fullStr Serum markers in early-stage and locally advanced melanoma
title_full_unstemmed Serum markers in early-stage and locally advanced melanoma
title_short Serum markers in early-stage and locally advanced melanoma
title_sort serum markers in early-stage and locally advanced melanoma
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4672018/
https://www.ncbi.nlm.nih.gov/pubmed/26002577
http://dx.doi.org/10.1007/s13277-015-3564-2
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