The Clinical Respiratory Journal (Aug 2024)

Predictive Value of Lymphocyte‐to‐Neutrophil Ratio and Platelet‐to‐Neutrophil Ratio on PD‐L1 Expression in Lung Cancer

  • Shun‐Shun Cui,
  • Ya Shen,
  • Rui‐Qing Yang

DOI
https://doi.org/10.1111/crj.13821
Journal volume & issue
Vol. 18, no. 8
pp. n/a – n/a

Abstract

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ABSTRACT Objective This study aimed to examine the predictive effect of the lymphocyte‐to‐neutrophil ratio (LNR) and the platelet‐to‐neutrophil ratio (PNR) on the expression of programmed death receptor ligand 1 (PD‐L1) in patients diagnosed with lung cancer. Methods The clinical records of 86 patients diagnosed with lung cancer between January 2020 and February 2022 at Fu Yang People's Hospital were retrospectively analyzed. The records included information on age, gender, smoking history, hematological indices at the time of admission, staging of the lung malignancy, histopathological subtype, comorbidities, and the expression levels of PD‐L1. Patients were stratified into two distinct cohorts based on their PD‐L1 expression levels: Those with an expression level greater than or equal to 1% were classified into the PD‐L1 positive expression group, while the remainder were categorized as the PD‐L1 negative expression group. Univariate analysis and multivariate logistic regression analysis were used to identify the influencing factors of PD‐L1, and the diagnostic efficacy was calculated using the receiver operating characteristic (ROC) curve. Results Upon analysis, the PD‐L1 positive expression group manifested notably lower values as compared to their counterparts in the PD‐L1 negative expression group (LNR: 0.262 ± 0.105 vs. 0.390 ± 0.201; PNR: 41.03 [29.64, 50.11] vs. 49.50 [37.38, 73.83]), and these differences were statistically significant. There was a notable disparity in PD‐L1 expression based on gender, with males exhibiting a statistically significant higher positivity rate compared to females. Furthermore, patients in Stages I–III of the disease demonstrated a markedly elevated PD‐L1 positivity rate compared to those in Stage IV (p < 0.05). Incorporating univariates with statistical differences into multivariate logistic regression analysis suggests that stage and LNR are independent risk factors for PD‐L1 negative expression. ROC curve analyses revealed that the area under the ROC curve (AUC) for LNR as an indicator for PD‐L1 positive expression stood at 0.706, while the AUC for PNR was calculated at 0.687. Conclusion PD‐L1 expression is correlated with gender and lung cancer staging, and LNR and PNR have a predictive value for PD‐L1 expression.

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