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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Abbreviations
- AJCC:
-
American Joint Committee on Cancer
- CCL17:
-
Chemokine (C–C motif) ligand 17
- CCR4:
-
C–C chemokine receptor type 4
- CMMR:
-
Central Malignant Melanoma Registry
- IQR:
-
Inter-quartile range
- Tregs:
-
Regulatory T cells
- LDH:
-
Lactate dehydrogenase
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Acknowledgments
This work was supported by the collaborative research center (CRC/SFB) 685 of the German Research Foundation (DFG) to Dominik Hartl.
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All authors declare that no conflict of interest exists.
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Weide, B., Allgaier, N., Hector, A. et al. Increased CCL17 serum levels are associated with improved survival in advanced melanoma. Cancer Immunol Immunother 64, 1075–1082 (2015). https://doi.org/10.1007/s00262-015-1714-4
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DOI: https://doi.org/10.1007/s00262-015-1714-4