Baseline and changes in inflammatory parameters for patients with EGFR-mutated NSCLC treated with afatinib

Zi Ting Chang, Ping Chih Hsu, How Wen Ko, John Wen Cheng Chang, Chen Te Wu, Chen Yang Huang, Ching Fu Chang, Chih Hsi Scott Kuo, Cheng Ta Yang, Chiao En Wu*

*Corresponding author for this work

Research output: Contribution to journalJournal Article peer-review

Abstract

BACKGROUND: This study investigated the relationship between inflammatory biomarkers (lymphocyte ratio [NLR], monocyte-to-lymphocyte ratio [MLR], and platelet-to-lymphocyte ratio [PLR]) and the treatment outcomes of patients with non-small cell lung cancer (NSCLC) treated with afatinib.

METHODS: The patients with NSCLC treated with afatinib between June 2014 and February 2018 were retrospectively reviewed. Their inflammatory biomarkers and clinical outcomes (progression-free survival [PFS] and tumor response) were explored using univariate and multivariate analyses.

RESULTS: Among 325 patients, those with an NLR >2.18, MLR >0.19, and PLR >177.73 had significantly worse PFS than those with lower values. After adjusting for performance status, stage, and liver metastasis, the PFS was still unfavorable for a baseline NLR >2.18, MLR >0.19, or PLR > 177.73. Among 188 patients with paired inflammatory values, those whose NLR decreased by >29.5%, MLR decreased by >57.9%, and PLR increased by <18.8% had significantly better PFS. After adjusting for performance status, stage, and liver metastasis, the PFS was significantly unfavorable for an NLR decrease of <29.5% and MLR decrease of <57.9%. Among the patients with tumor response, NLR, MLR, and PLR significantly decreased after treatment (all p < 0.05).

CONCLUSIONS: Our study presented the NLR, MLR, and PLR as prognostic factors for patients with NSCLC treated with afatinib. Further investigation into these markers representing the tumor microenvironment and their association with cancer status is crucial for evaluating prognosis and clinical outcomes in patients with NSCLC.

Original languageEnglish
Article numbere15338
Pages (from-to)e15338
JournalThoracic Cancer
Volume16
Issue number13
Early online date17 04 2025
DOIs
StatePublished - 07 2025

Bibliographical note

Publisher Copyright:
© 2025 The Author(s). Thoracic Cancer published by John Wiley & Sons Australia, Ltd.

Keywords

  • Adult
  • Afatinib/therapeutic use
  • Aged
  • Aged, 80 and over
  • Carcinoma, Non-Small-Cell Lung/drug therapy
  • ErbB Receptors/genetics
  • Female
  • Humans
  • Inflammation/pathology
  • Lung Neoplasms/drug therapy
  • Male
  • Middle Aged
  • Mutation
  • Prognosis
  • Retrospective Studies

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