Cargando…

Immunological inflammatory biomarkers as prognostic predictors for advanced hepatocellular carcinoma

BACKGROUND: The immunological inflammatory biomarkers for advanced hepatocellular carcinoma are unclear. We aimed to investigate the association of immunity and inflammatory status with treatment outcomes in patients with advanced hepatocellular carcinoma who received molecular-targeted agents as pr...

Descripción completa

Detalles Bibliográficos
Autores principales: Nakano, M., Kuromatsu, R., Niizeki, T., Okamura, S., Iwamoto, H., Shimose, S., Shirono, T., Noda, Y., Kamachi, N., Koga, H., Torimura, T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7807940/
https://www.ncbi.nlm.nih.gov/pubmed/33399083
http://dx.doi.org/10.1016/j.esmoop.2020.100020
_version_ 1783636839363510272
author Nakano, M.
Kuromatsu, R.
Niizeki, T.
Okamura, S.
Iwamoto, H.
Shimose, S.
Shirono, T.
Noda, Y.
Kamachi, N.
Koga, H.
Torimura, T.
author_facet Nakano, M.
Kuromatsu, R.
Niizeki, T.
Okamura, S.
Iwamoto, H.
Shimose, S.
Shirono, T.
Noda, Y.
Kamachi, N.
Koga, H.
Torimura, T.
author_sort Nakano, M.
collection PubMed
description BACKGROUND: The immunological inflammatory biomarkers for advanced hepatocellular carcinoma are unclear. We aimed to investigate the association of immunity and inflammatory status with treatment outcomes in patients with advanced hepatocellular carcinoma who received molecular-targeted agents as primary treatment. PATIENTS AND METHODS: We enrolled 728 consecutive patients with advanced hepatocellular carcinoma who received sorafenib (n = 554) or lenvatinib (n = 174) as primary treatment in Japan between May 2009 and June 2020. Changes in the neutrophil-to-lymphocyte ratio before and 1 month after treatment and their impact on survival were evaluated. The cut-off values of neutrophil-to-lymphocyte ratio and platelet-to-lymphocyte ratio for predicting overall and progression-free survival were calculated using receiver operating characteristic curves. RESULTS: The neutrophil-to-lymphocyte ratio, but not the platelet-to-lymphocyte ratio, was an independent prognostic factor. Patients with decreased neutrophil-to-lymphocyte ratio survived significantly longer than patients with increased neutrophil-to-lymphocyte ratio (median overall survival: 14.7 versus 10.4 months, P = 0.0110). Among patients with a low pre-treatment neutrophil-to-lymphocyte ratio, the overall survival did not differ significantly between those with decreased and those with increased neutrophil-to-lymphocyte ratio after 1 month (median: 19.0 versus 14.8 months, P = 0.1498). However, among patients with high pre-treatment neutrophil-to-lymphocyte ratio, those whose neutrophil-to-lymphocyte ratio decreased after 1 month showed significantly longer survival than those whose neutrophil-to-lymphocyte ratio increased (median: 12.7 versus 5.5 months, P < 0.0001). The therapeutic effect was not correlated with pre-treatment neutrophil-to-lymphocyte ratio or platelet-to-lymphocyte ratio. CONCLUSIONS: The neutrophil-to-lymphocyte ratio is a prognostic factor, along with liver function and tumor markers, in patients with advanced hepatocellular carcinoma who received molecular-targeted agents as primary treatment. Thus, the neutrophil-to-lymphocyte ratio could be a prognostic biomarker for advanced hepatocellular carcinoma primarily treated with immunotherapy.
format Online
Article
Text
id pubmed-7807940
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Elsevier
record_format MEDLINE/PubMed
spelling pubmed-78079402021-01-22 Immunological inflammatory biomarkers as prognostic predictors for advanced hepatocellular carcinoma Nakano, M. Kuromatsu, R. Niizeki, T. Okamura, S. Iwamoto, H. Shimose, S. Shirono, T. Noda, Y. Kamachi, N. Koga, H. Torimura, T. ESMO Open Original Research BACKGROUND: The immunological inflammatory biomarkers for advanced hepatocellular carcinoma are unclear. We aimed to investigate the association of immunity and inflammatory status with treatment outcomes in patients with advanced hepatocellular carcinoma who received molecular-targeted agents as primary treatment. PATIENTS AND METHODS: We enrolled 728 consecutive patients with advanced hepatocellular carcinoma who received sorafenib (n = 554) or lenvatinib (n = 174) as primary treatment in Japan between May 2009 and June 2020. Changes in the neutrophil-to-lymphocyte ratio before and 1 month after treatment and their impact on survival were evaluated. The cut-off values of neutrophil-to-lymphocyte ratio and platelet-to-lymphocyte ratio for predicting overall and progression-free survival were calculated using receiver operating characteristic curves. RESULTS: The neutrophil-to-lymphocyte ratio, but not the platelet-to-lymphocyte ratio, was an independent prognostic factor. Patients with decreased neutrophil-to-lymphocyte ratio survived significantly longer than patients with increased neutrophil-to-lymphocyte ratio (median overall survival: 14.7 versus 10.4 months, P = 0.0110). Among patients with a low pre-treatment neutrophil-to-lymphocyte ratio, the overall survival did not differ significantly between those with decreased and those with increased neutrophil-to-lymphocyte ratio after 1 month (median: 19.0 versus 14.8 months, P = 0.1498). However, among patients with high pre-treatment neutrophil-to-lymphocyte ratio, those whose neutrophil-to-lymphocyte ratio decreased after 1 month showed significantly longer survival than those whose neutrophil-to-lymphocyte ratio increased (median: 12.7 versus 5.5 months, P < 0.0001). The therapeutic effect was not correlated with pre-treatment neutrophil-to-lymphocyte ratio or platelet-to-lymphocyte ratio. CONCLUSIONS: The neutrophil-to-lymphocyte ratio is a prognostic factor, along with liver function and tumor markers, in patients with advanced hepatocellular carcinoma who received molecular-targeted agents as primary treatment. Thus, the neutrophil-to-lymphocyte ratio could be a prognostic biomarker for advanced hepatocellular carcinoma primarily treated with immunotherapy. Elsevier 2021-01-04 /pmc/articles/PMC7807940/ /pubmed/33399083 http://dx.doi.org/10.1016/j.esmoop.2020.100020 Text en © 2020 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Research
Nakano, M.
Kuromatsu, R.
Niizeki, T.
Okamura, S.
Iwamoto, H.
Shimose, S.
Shirono, T.
Noda, Y.
Kamachi, N.
Koga, H.
Torimura, T.
Immunological inflammatory biomarkers as prognostic predictors for advanced hepatocellular carcinoma
title Immunological inflammatory biomarkers as prognostic predictors for advanced hepatocellular carcinoma
title_full Immunological inflammatory biomarkers as prognostic predictors for advanced hepatocellular carcinoma
title_fullStr Immunological inflammatory biomarkers as prognostic predictors for advanced hepatocellular carcinoma
title_full_unstemmed Immunological inflammatory biomarkers as prognostic predictors for advanced hepatocellular carcinoma
title_short Immunological inflammatory biomarkers as prognostic predictors for advanced hepatocellular carcinoma
title_sort immunological inflammatory biomarkers as prognostic predictors for advanced hepatocellular carcinoma
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7807940/
https://www.ncbi.nlm.nih.gov/pubmed/33399083
http://dx.doi.org/10.1016/j.esmoop.2020.100020
work_keys_str_mv AT nakanom immunologicalinflammatorybiomarkersasprognosticpredictorsforadvancedhepatocellularcarcinoma
AT kuromatsur immunologicalinflammatorybiomarkersasprognosticpredictorsforadvancedhepatocellularcarcinoma
AT niizekit immunologicalinflammatorybiomarkersasprognosticpredictorsforadvancedhepatocellularcarcinoma
AT okamuras immunologicalinflammatorybiomarkersasprognosticpredictorsforadvancedhepatocellularcarcinoma
AT iwamotoh immunologicalinflammatorybiomarkersasprognosticpredictorsforadvancedhepatocellularcarcinoma
AT shimoses immunologicalinflammatorybiomarkersasprognosticpredictorsforadvancedhepatocellularcarcinoma
AT shironot immunologicalinflammatorybiomarkersasprognosticpredictorsforadvancedhepatocellularcarcinoma
AT noday immunologicalinflammatorybiomarkersasprognosticpredictorsforadvancedhepatocellularcarcinoma
AT kamachin immunologicalinflammatorybiomarkersasprognosticpredictorsforadvancedhepatocellularcarcinoma
AT kogah immunologicalinflammatorybiomarkersasprognosticpredictorsforadvancedhepatocellularcarcinoma
AT torimurat immunologicalinflammatorybiomarkersasprognosticpredictorsforadvancedhepatocellularcarcinoma