Abstract

A higher platelet-to-lymphocyte ratio (PLR) has a clinical correlation with shorter survival in non-small cell lung cancer (NSCLC). The present study evaluated the association between the PLR and survival in patients with advanced NSCLC with malignant pleural effusion (MPE). Between January 2012 and July 2016, 237 patients with stage IV NSCLC were selected for evaluation. Receiver operating characteristic analysis was used to determine a cutoff for the PLR. Clinicopathological characteristics were compared between the high and low PLR groups, and the role of PLR as a predictive/prognostic maker was investigated. Among the 237 patients, 122 were assigned to the low PLR group and the other 115 to the high PLR group. According to multivariate analysis, male sex, not receiving active anticancer treatment, low hemoglobin level, low albumin level, high C-reactive protein level, and high PLR were identified as significant risk factors for shorter overall survival (OS) (p = 0.010, <0.001, 0.011, 0.004, 0.003, and <0.001, respectively). In the subgroup multivariate analysis of driver mutation-negative NSCLC, high Eastern Cooperative Oncology Group score, not receiving active anticancer treatment, low hemoglobin level, high C-reactive protein level, and high PLR were identified as significant risk factors for shorter OS (p = 0.047, <0.001, = 0.036, = 0.003, and <0.001, respectively). A high pretreatment PLR is independently associated with poor survival in stage IV NSCLC with MPE and in a subgroup of epidermal growth factor receptor and anaplastic lymphoma kinase wild-type NSCLC.

Highlights

  • Lung cancer is one of the leading causes of cancer death worldwide[1]

  • There was no significant difference in progression-free survival (PFS) between the two groups

  • The present study showed that a higher platelet-to-lymphocyte ratio (PLR) was an independent predictor of shorter survival of stage IV non-small cell lung cancer (NSCLC) patients with malignant pleural effusion (MPE)

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Summary

Introduction

Lung cancer is one of the leading causes of cancer death worldwide[1]. Non-small cell lung cancer (NSCLC) comprises 85% of all lung cancers[2]. The predictive and prognostic values of PLR have been evaluated in both advanced www.nature.com/scientificreports/. NSCLC patients with MPE show poor prognosis with a median survival time of less than 12 months[20], and complain more respiratory symptoms which lead to decreased quality of life[21]. While they show distinct and more unfavorable clinical manifestations, evaluation of prognostic values of PLR in this subgroup of advanced NSCLC is meaningful. The prognostic and predictive values of PLR in patients with epidermal growth factor receptor (EGFR) and anaplastic lymphoma kinase (ALK) wild-type NSCLC have not been investigated. Crizotinib therapy improved the survival of patients with ALK-positive NSCLC compared with those not treated with crizotinib[23]

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