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Erschienen in: Cancer Immunology, Immunotherapy 9/2015

01.09.2015 | Original Article

Increased CCL17 serum levels are associated with improved survival in advanced melanoma

verfasst von: Benjamin Weide, Nicolas Allgaier, Andreas Hector, Andrea Forschner, Ulrike Leiter, Thomas K. Eigentler, Claus Garbe, Dominik Hartl

Erschienen in: Cancer Immunology, Immunotherapy | Ausgabe 9/2015

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Abstract

Background

Prognostic factors of melanoma patients with distant metastases remain poorly established. This study aimed to compare the prognostic impact of putative serum biomarkers, namely S100B, YKL-40 or CCL17, in stage IV melanoma patients.

Patients and methods

Serum concentrations were analyzed by ELISA. Disease-specific survival of 80 patients according to S100B, YKL-40 or CCL17 and clinical factors were calculated by univariate Kaplan–Meier survival and multivariate analysis.

Results

Low serum levels of S100B, high concentrations of CCL17 and female gender correlated with improved survival. A trend for favorable prognosis was observed for the M categories M1a/b versus M1c according to the AJCC classification. No correlation with survival was evident for YKL-40 serum levels and age. In multivariate analysis, S100B (HR 2.1; p = 0.005) and CCL17 (HR 1.8; p = 0.029) had independent prognostic impact. Patients with a combination of normal S100B and high CCL17 had a high chance for long-term survival, which was 43 % after 3 years.

Conclusion

Serum levels of CCL17 and S100B represent independent prognostic markers for melanoma patients with distant metastases. These biomarkers were more powerful than the M category according to the AJCC classification to indicate overall survival. CCL17 represents a promising biomarker upon immune checkpoint blockade in melanoma.
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Metadaten
Titel
Increased CCL17 serum levels are associated with improved survival in advanced melanoma
verfasst von
Benjamin Weide
Nicolas Allgaier
Andreas Hector
Andrea Forschner
Ulrike Leiter
Thomas K. Eigentler
Claus Garbe
Dominik Hartl
Publikationsdatum
01.09.2015
Verlag
Springer Berlin Heidelberg
Erschienen in
Cancer Immunology, Immunotherapy / Ausgabe 9/2015
Print ISSN: 0340-7004
Elektronische ISSN: 1432-0851
DOI
https://doi.org/10.1007/s00262-015-1714-4

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