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Platelet-to-lymphocyte ratio acts as a prognostic factor for patients with advanced hepatocellular carcinoma

Authors :
Tian-Tian Wang
Yun Deng
Xing Li
Ze-Xiao Lin
Li Wei
Xiao-Kun Ma
Yan-Fang Xing
Xiang-Yuan Wu
Zhan-Hong Chen
Dong-Hao Wu
Jin-Yun Wen
Jie Chen
Min Dong
Dan-Yun Ruan
Qu Lin
Source :
Tumor Biology. 36:2263-2269
Publication Year :
2014
Publisher :
Springer Science and Business Media LLC, 2014.

Abstract

The platelet count, as an inflammation marker, is involved in the progress of tumor invasion. However, the prognostic value of platelet counts and the platelet-to-lymphocyte ratio (PLR) has not been investigated in patients with advanced hepatocellular carcinoma (HCC). This study aimed to determine the prognostic value of platelet counts and PLR in HCC patients. A total of 243 ethnic Chinese advanced HCC patients from two major hospitals, not receiving systemic sorafenib, were analyzed retrospectively. The prognostic value of differential blood cell counts and PLR for overall survival (OS) was determined by integrating the Cancer of the Liver Italian Program (CLIP) score system and model for end-stage liver disease by using a stepwise model of multivariate Cox regression. The Kaplan-Meier method and receiver operating characteristic (ROC) curves were utilized accordingly. PLR was confirmed to be an independent predictor for OS (p 0.01), while the remaining parameters had no predictive value. Then, advanced HCC patients were dichotomized into two groups based on the PLR value (≤111.23 or111.23), according to ROC analysis. Patients with a high PLR had a lower 3-month survival rate (37.6 vs. 57.6%) compared with patients with a low PLR. PLR was associated with aggressive malignant behavior, characterized by distant metastasis and portal vein thrombosis. Additionally, PLR was not associated with the CLIP score and Child-Pugh grade. PLR was identified as an independent prognostic factor for advanced HCC patients not receiving systemic sorafenib; the predictive ability of PLR partially relies on its association with the aggressive nature of HCC.

Details

ISSN :
14230380 and 10104283
Volume :
36
Database :
OpenAIRE
Journal :
Tumor Biology
Accession number :
edsair.doi.dedup.....25a463cf9a98f98cd93bc988a9461d22
Full Text :
https://doi.org/10.1007/s13277-014-2833-9