Abstract

Objective Inflammation-driven markers play a crucial role in tumorigenesis and tumor progression. The neutrophil-to-lymphocyte ratio (NLR) and platelet-to-lymphocyte ratio (PLR) in blood are systemic inflammatory response markers. Some reports have showed that NLR and PLR are related to a poor prognosis in patients with lung cancer. However, little studies have reported whether NLR and PLR can be diagnostic markers for lung cancer. The aim of the current study is to investigate the roles of NLR and PLR in diagnosing lung cancer. Methods This study analyzed data from lung cancer patients and healthy individuals in Wuxi People's Hospital Affiliated with Nanjing Medical University. The Mann–Whitney U test was performed to compare differences between the lung cancer group and the control group. Based on white blood cell (WBC) counts, both lung cancer patients and healthy individuals were divided into the low-level group, moderate-level group, and high-level group. The Kruskal-Wallis test was applied to compare differences of NLR and PLR among those groups with different WBC counts. Spearman correlation analysis was used to assess correlations. Receiver operating characteristic (ROC) curves were performed to determine diagnostic accuracy. Results 210 patients diagnosed with lung cancer and 261 healthy subjects were enrolled in this study. Levels of NLR and PLR increased in the lung cancer group compared with the control group (P < 0.001). For the lung cancer group, NLR levels could rise with the increasing of WBC levels (P < 0.001) while PLR levels had no significant variation with the increasing of WBC levels (P = 0.206). For the control group, NLR levels could rise with the increasing of WBC levels (P < 0.001) while PLR levels would decline with the increasing of WBC levels (P < 0.001). In the lung cancer group, both NLR and PLR had no significant correlations with aspartate transaminase, urea, and glucose. The area under the curve (AUC) with 95% confidence interval (95% CI) of NLR and PLR to distinguish lung cancer patients from healthy subjects was, respectively, 0.684 (0.634-0.735) and 0.623 (0.571-0.674). When NLR and PLR were combined, AUC (95% CI) increased to 0.691 (0.642-0.740). Conclusions NLR and PLR alone have moderate ability to distinguish lung cancer patients from healthy subjects. Furthermore, combination forms of NLR and PLR can improve diagnostic ability.

Highlights

  • According to Global Cancer Statistics 2018, lung cancer is a leading cause of newly diagnosed cancer and deaths across 20 regions of the world [1]

  • HGB, red blood cell distribution width (RDW), and platelet distribution width (PDW) were significantly lower in the lung cancer group compared to the control group (P < 0:001), while white blood cell (WBC) was significantly higher in the lung cancer group (P = 0:001)

  • For the lung cancer group, neutrophil-to-lymphocyte ratio (NLR) levels could rise with the increasing of WBC levels (P < 0:001) while platelet-to-lymphocyte ratio (PLR) levels had no significant variation with the increasing of WBC levels (P = 0:206)

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Summary

Introduction

According to Global Cancer Statistics 2018, lung cancer is a leading cause of newly diagnosed cancer and deaths across 20 regions of the world [1]. 23% of new deaths per year for men and women, respectively [2]. Lung cancer represents a major worldwide disease burden and will continue to be a major health problem through the first half of this century [3]. Inflammation is an important component of the tumor microenvironment, and selected chronic inflammatory conditions increase the risk of developing cancer [4]. Inflammation-driven markers play a crucial role in tumorigenesis and tumor progression [5]. The systemic inflammation score, a systemic inflammatory marker based on the lymphocyte-to-monocyte ratio and serum albumin level, might serve as an independent biomarker for predicting adverse events and prognosis in locally advanced rectal cancer [6]

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