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The Combination of Neutrophil–Lymphocyte Ratio and Platelet–Lymphocyte Ratio with Liquid Biopsy Biomarkers Improves Prognosis Prediction in Metastatic Pancreatic Cancer

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Author
Toledano-Fonseca, Marta
Cano, M. Teresa
Inga, Elizabeth
Gómez-España, M. Auxiliadora
Guil-Luna, Silvia
García-Ortiz, M.V.
Mena-Osuna, Rafael
Haba-Rodríguez, Juan R. de la
Rodríguez-Ariza, Antonio
Aranda Aguilar, Enrique
Publisher
MDPI
Date
2021
Subject
NLR
PLR
Circulating tumor DNA
Pancreatic ductal adenocarcinoma
RAS mutation
Neutrophil elastase
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Abstract
Pancreatic ductal adenocarcinoma (PDAC) is an aggressive cancer with a highly inflammatory microenvironment and liquid biopsy has emerged as a promising tool for the noninvasive analysis of this tumor. In this study, plasma was obtained from 58 metastatic PDAC patients, and neutrophil–lymphocyte ratio (NLR), platelet–lymphocyte ratio (PLR), circulating cell-free DNA (cfDNA) concentration, and circulating RAS mutation were determined. We found that NLR was significantly associated with both overall survival (OS) and progression-free survival. Remarkably, NLR was an independent risk factor for poor OS. Moreover, NLR and PLR positively correlated, and combination of both inflammatory markers significantly improved the prognostic stratification of metastatic PDAC patients. NLR also showed a positive correlation with cfDNA levels and RAS mutant allelic fraction (MAF). Besides, we found that neutrophil activation contributed to cfDNA content in the plasma of metastatic PDAC patients. Finally, a multi-parameter prognosis model was designed by combining NLR, PLR, cfDNA levels, RAS mutation, RAS MAF, and CA19-9, which performs as a promising tool to predict the prognosis of metastatic PDAC patients. In conclusion, our study supports the idea that the use of systemic inflammatory markers along with circulating tumor-specific markers may constitute a valuable tool for the clinical management of metastatic PDAC patients.
URI
http://hdl.handle.net/10396/21157
Fuente
Cancers 13(6), 1210 (2021)
Versión del Editor
http://dx.doi.org/10.3390/cancers13061210
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