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中性粒细胞与淋巴细胞比值和血小板与淋巴细胞比值联合液体活检生物标志物可改善转移性胰腺癌的预后预测。

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

作者信息

Toledano-Fonseca Marta, Cano M Teresa, Inga Elizabeth, Gómez-España Auxiliadora, Guil-Luna Silvia, García-Ortiz María Victoria, Mena-Osuna Rafael, De la Haba-Rodriguez Juan R, Rodríguez-Ariza Antonio, Aranda Enrique

机构信息

Maimonides Biomedical Research Institute of Cordoba (IMIBIC), 14004 Córdoba, Spain.

Cancer Network Biomedical Research Centre (CIBERONC), 28029 Madrid, Spain.

出版信息

Cancers (Basel). 2021 Mar 10;13(6):1210. doi: 10.3390/cancers13061210.

DOI:10.3390/cancers13061210
PMID:33802006
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7998484/
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.

摘要

胰腺导管腺癌(PDAC)是一种侵袭性癌症,具有高度炎症性的微环境,而液体活检已成为对该肿瘤进行无创分析的一种有前景的工具。在本研究中,从58例转移性PDAC患者中获取血浆,测定中性粒细胞与淋巴细胞比率(NLR)、血小板与淋巴细胞比率(PLR)、循环游离DNA(cfDNA)浓度以及循环RAS突变。我们发现NLR与总生存期(OS)和无进展生存期均显著相关。值得注意的是,NLR是OS不良的独立危险因素。此外,NLR与PLR呈正相关,两种炎症标志物的联合显著改善了转移性PDAC患者的预后分层。NLR还与cfDNA水平和RAS突变等位基因分数(MAF)呈正相关。此外,我们发现中性粒细胞活化促成了转移性PDAC患者血浆中的cfDNA含量。最后,通过结合NLR、PLR、cfDNA水平、RAS突变、RAS MAF和CA19-9设计了一个多参数预后模型,该模型是预测转移性PDAC患者预后的一种有前景的工具。总之,我们的研究支持这样一种观点,即使用全身炎症标志物以及循环肿瘤特异性标志物可能构成用于转移性PDAC患者临床管理的有价值工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e074/7998484/238cfceeec58/cancers-13-01210-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e074/7998484/d6ff82a9f7fb/cancers-13-01210-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e074/7998484/fe3b2f14290c/cancers-13-01210-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e074/7998484/ba55300c6059/cancers-13-01210-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e074/7998484/6c039dc617f5/cancers-13-01210-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e074/7998484/d64449e29507/cancers-13-01210-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e074/7998484/4ab2c1556606/cancers-13-01210-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e074/7998484/1d04d4d32761/cancers-13-01210-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e074/7998484/238cfceeec58/cancers-13-01210-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e074/7998484/d6ff82a9f7fb/cancers-13-01210-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e074/7998484/fe3b2f14290c/cancers-13-01210-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e074/7998484/ba55300c6059/cancers-13-01210-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e074/7998484/6c039dc617f5/cancers-13-01210-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e074/7998484/d64449e29507/cancers-13-01210-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e074/7998484/4ab2c1556606/cancers-13-01210-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e074/7998484/1d04d4d32761/cancers-13-01210-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e074/7998484/238cfceeec58/cancers-13-01210-g008.jpg

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