A serum protein signature at the time of Uveal Melanoma diagnosis predicts long-term patient survival

Abstract Purpose To develop a prognostic test based on a single blood sample obtained at the time of uveal melanoma diagnosis. Methods 83 patients diagnosed with posterior uveal melanoma between 1996 and 2000 were included. Peripheral serum samples were obtained at diagnosis and kept at -80 °C until...

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Main Authors: Christina Herrspiegel, Flavia Plastino, Emma Lardner, Stefan Seregard, Pete A. Williams, Helder André, Gustav Stålhammar
Format: Article
Language:English
Published: BMC 2023-03-01
Series:BMC Cancer
Subjects:
Online Access:https://doi.org/10.1186/s12885-023-10757-x
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author Christina Herrspiegel
Flavia Plastino
Emma Lardner
Stefan Seregard
Pete A. Williams
Helder André
Gustav Stålhammar
author_facet Christina Herrspiegel
Flavia Plastino
Emma Lardner
Stefan Seregard
Pete A. Williams
Helder André
Gustav Stålhammar
author_sort Christina Herrspiegel
collection DOAJ
description Abstract Purpose To develop a prognostic test based on a single blood sample obtained at the time of uveal melanoma diagnosis. Methods 83 patients diagnosed with posterior uveal melanoma between 1996 and 2000 were included. Peripheral serum samples were obtained at diagnosis and kept at -80 °C until this analysis. Protein profiling of 84 cancer-related proteins was used to screen for potential biomarkers and a prognostic test that stratifies patients into metastatic risk categories was developed (serUM-Px) in a training cohort and then tested in a validation cohort. Results Low serum leptin levels and high osteopontin levels were found to identify patients with poor prognosis and were therefore selected for inclusion in the final test. In the validation cohort, patient sex and American Joint Committee on Cancer stages were similarly distributed between the low, intermediate, and high metastatic risk categories. With increasing metastatic risk category, patients had shorter metastasis-free- and overall survival, as well as greater cumulative incidence of uveal melanoma-related mortality in competing risk analysis (P = 0.007, 0.018 and 0.029, respectively). In multivariate Cox regression, serUM-Px was an independent predictor of metastasis with tumor size and patient sex as covariates (hazard ratio 3.2, 95% CI 1.5–6.9). Conclusions A prognostic test based on a single peripheral venous blood sample at the time of uveal melanoma diagnosis stratifies patients into low, intermediate, and high metastatic risk categories. Prospective validation will facilitate its clinical utility.
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spelling doaj.art-dfb5ef89f6d14bec8ec1dc4e25f047dc2023-04-03T05:30:41ZengBMCBMC Cancer1471-24072023-03-0123111510.1186/s12885-023-10757-xA serum protein signature at the time of Uveal Melanoma diagnosis predicts long-term patient survivalChristina Herrspiegel0Flavia Plastino1Emma Lardner2Stefan Seregard3Pete A. Williams4Helder André5Gustav Stålhammar6St. Erik Eye HospitalDepartment of Clinical Neuroscience, Division of Eye and Vision, Karolinska InstitutetSt. Erik Eye HospitalSt. Erik Eye HospitalSt. Erik Eye HospitalDepartment of Clinical Neuroscience, Division of Eye and Vision, Karolinska InstitutetSt. Erik Eye HospitalAbstract Purpose To develop a prognostic test based on a single blood sample obtained at the time of uveal melanoma diagnosis. Methods 83 patients diagnosed with posterior uveal melanoma between 1996 and 2000 were included. Peripheral serum samples were obtained at diagnosis and kept at -80 °C until this analysis. Protein profiling of 84 cancer-related proteins was used to screen for potential biomarkers and a prognostic test that stratifies patients into metastatic risk categories was developed (serUM-Px) in a training cohort and then tested in a validation cohort. Results Low serum leptin levels and high osteopontin levels were found to identify patients with poor prognosis and were therefore selected for inclusion in the final test. In the validation cohort, patient sex and American Joint Committee on Cancer stages were similarly distributed between the low, intermediate, and high metastatic risk categories. With increasing metastatic risk category, patients had shorter metastasis-free- and overall survival, as well as greater cumulative incidence of uveal melanoma-related mortality in competing risk analysis (P = 0.007, 0.018 and 0.029, respectively). In multivariate Cox regression, serUM-Px was an independent predictor of metastasis with tumor size and patient sex as covariates (hazard ratio 3.2, 95% CI 1.5–6.9). Conclusions A prognostic test based on a single peripheral venous blood sample at the time of uveal melanoma diagnosis stratifies patients into low, intermediate, and high metastatic risk categories. Prospective validation will facilitate its clinical utility.https://doi.org/10.1186/s12885-023-10757-xUveal melanomaChoroidal melanomaLiquid biopsySerum sampleProteomePrognosis
spellingShingle Christina Herrspiegel
Flavia Plastino
Emma Lardner
Stefan Seregard
Pete A. Williams
Helder André
Gustav Stålhammar
A serum protein signature at the time of Uveal Melanoma diagnosis predicts long-term patient survival
BMC Cancer
Uveal melanoma
Choroidal melanoma
Liquid biopsy
Serum sample
Proteome
Prognosis
title A serum protein signature at the time of Uveal Melanoma diagnosis predicts long-term patient survival
title_full A serum protein signature at the time of Uveal Melanoma diagnosis predicts long-term patient survival
title_fullStr A serum protein signature at the time of Uveal Melanoma diagnosis predicts long-term patient survival
title_full_unstemmed A serum protein signature at the time of Uveal Melanoma diagnosis predicts long-term patient survival
title_short A serum protein signature at the time of Uveal Melanoma diagnosis predicts long-term patient survival
title_sort serum protein signature at the time of uveal melanoma diagnosis predicts long term patient survival
topic Uveal melanoma
Choroidal melanoma
Liquid biopsy
Serum sample
Proteome
Prognosis
url https://doi.org/10.1186/s12885-023-10757-x
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