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Systemic immune-inflammation index in germ-cell tumours

BACKGROUND: We evaluated systemic immune-inflammation index (SII) and its association with patient outcome in germ-cell tumours (GCTs). METHODS: Two independent cohorts of patients were analysed; the discovery set (n=171) from a single institution and the validation set (n=181) previously included i...

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Autores principales: Chovanec, Michal, Cierna, Zuzana, Miskovska, Viera, Machalekova, Katarina, Kalavska, Katarina, Rejlekova, Katarina, Svetlovska, Daniela, Macak, Dusan, Spanik, Stanislav, Kajo, Karol, Babal, Pavel, De Giorgi, Ugo, Mego, Michal, Mardiak, Jozef
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5877428/
https://www.ncbi.nlm.nih.gov/pubmed/29485980
http://dx.doi.org/10.1038/bjc.2017.460
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author Chovanec, Michal
Cierna, Zuzana
Miskovska, Viera
Machalekova, Katarina
Kalavska, Katarina
Rejlekova, Katarina
Svetlovska, Daniela
Macak, Dusan
Spanik, Stanislav
Kajo, Karol
Babal, Pavel
De Giorgi, Ugo
Mego, Michal
Mardiak, Jozef
author_facet Chovanec, Michal
Cierna, Zuzana
Miskovska, Viera
Machalekova, Katarina
Kalavska, Katarina
Rejlekova, Katarina
Svetlovska, Daniela
Macak, Dusan
Spanik, Stanislav
Kajo, Karol
Babal, Pavel
De Giorgi, Ugo
Mego, Michal
Mardiak, Jozef
author_sort Chovanec, Michal
collection PubMed
description BACKGROUND: We evaluated systemic immune-inflammation index (SII) and its association with patient outcome in germ-cell tumours (GCTs). METHODS: Two independent cohorts of patients were analysed; the discovery set (n=171) from a single institution and the validation set (n=181) previously included in a study evaluating PD-L1 in GCTs. The SII was calculated using platelet (P), neutrophil (N) and lymphocyte (L) counts before chemotherapy and correlated with survival using regression analyses and Kaplan–Meier method. RESULTS: In the discovery cohort, the SII was associated with poor risk clinical features. Patients with low SII had significantly longer progression-free survival (HR=0.22, 95% CI 0.12–0.41, P<0.001) and overall survival (OS) (HR=0.16, 95% CI 0.08–0.32, P<0.001) compared to high SII. This index was independent of International Germ Cell Cancer Collaborative Group criteria in multivariable Cox regression analysis for OS and was validated in an independent cohort. When combining PD-L1 expression on tumour infiltrating lymphocytes (TILs) and SII, we identified three distinctive prognostic groups. CONCLUSIONS: High SII was associated with poor outcome in GCTs. Combination of PD-L1 positive TILs and SII could further refine prognosis in GCTs.
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spelling pubmed-58774282019-03-20 Systemic immune-inflammation index in germ-cell tumours Chovanec, Michal Cierna, Zuzana Miskovska, Viera Machalekova, Katarina Kalavska, Katarina Rejlekova, Katarina Svetlovska, Daniela Macak, Dusan Spanik, Stanislav Kajo, Karol Babal, Pavel De Giorgi, Ugo Mego, Michal Mardiak, Jozef Br J Cancer Molecular Diagnostics BACKGROUND: We evaluated systemic immune-inflammation index (SII) and its association with patient outcome in germ-cell tumours (GCTs). METHODS: Two independent cohorts of patients were analysed; the discovery set (n=171) from a single institution and the validation set (n=181) previously included in a study evaluating PD-L1 in GCTs. The SII was calculated using platelet (P), neutrophil (N) and lymphocyte (L) counts before chemotherapy and correlated with survival using regression analyses and Kaplan–Meier method. RESULTS: In the discovery cohort, the SII was associated with poor risk clinical features. Patients with low SII had significantly longer progression-free survival (HR=0.22, 95% CI 0.12–0.41, P<0.001) and overall survival (OS) (HR=0.16, 95% CI 0.08–0.32, P<0.001) compared to high SII. This index was independent of International Germ Cell Cancer Collaborative Group criteria in multivariable Cox regression analysis for OS and was validated in an independent cohort. When combining PD-L1 expression on tumour infiltrating lymphocytes (TILs) and SII, we identified three distinctive prognostic groups. CONCLUSIONS: High SII was associated with poor outcome in GCTs. Combination of PD-L1 positive TILs and SII could further refine prognosis in GCTs. Nature Publishing Group 2018-03-20 2018-02-27 /pmc/articles/PMC5877428/ /pubmed/29485980 http://dx.doi.org/10.1038/bjc.2017.460 Text en Copyright © 2018 Cancer Research UK http://creativecommons.org/licenses/by-nc-sa/4.0/ From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 4.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/
spellingShingle Molecular Diagnostics
Chovanec, Michal
Cierna, Zuzana
Miskovska, Viera
Machalekova, Katarina
Kalavska, Katarina
Rejlekova, Katarina
Svetlovska, Daniela
Macak, Dusan
Spanik, Stanislav
Kajo, Karol
Babal, Pavel
De Giorgi, Ugo
Mego, Michal
Mardiak, Jozef
Systemic immune-inflammation index in germ-cell tumours
title Systemic immune-inflammation index in germ-cell tumours
title_full Systemic immune-inflammation index in germ-cell tumours
title_fullStr Systemic immune-inflammation index in germ-cell tumours
title_full_unstemmed Systemic immune-inflammation index in germ-cell tumours
title_short Systemic immune-inflammation index in germ-cell tumours
title_sort systemic immune-inflammation index in germ-cell tumours
topic Molecular Diagnostics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5877428/
https://www.ncbi.nlm.nih.gov/pubmed/29485980
http://dx.doi.org/10.1038/bjc.2017.460
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