Published March 1, 2021 | Version v.1
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Hematological parameters in EGFR-mutated advanced NSCLC patients treated with TKIs: predicting survival and toxicity

  • 1. Clinic for Medical Oncology, Institute for Oncology and Radiology of Serbia, Belgrade, Serbia
  • 2. Department of Pharmacology, Clinical Pharmacology and Toxicology, Faculty of Medicine, University of Belgrade, Belgrade, Serbia
  • 3. Department of Experimental Oncology, Institute for Oncology and Radiology of Serbia, Belgrade, Serbia
  • 4. Clinic for Radiation Oncology and Diagnostics, Department of Radiation Oncology, Institute for Oncology and Radiology of Serbia, Belgrade, Serbia

Description

Background: The aim of this study was to analyze the prognostic value of pre-treatment hematological parameters in EGFR-mutated non-small cell lung cancer patients treated with tyrosine-kinase inhibitors (TKIs). Patients and methods: Patients with EGFR mutations were treated with EGFR-TKIs in the first line until progression/unacceptable toxicity. Hematological parameters were derived from the absolute baseline differential counts of a complete blood count. The associations between the patients’ and tumor characteristics were analyzed using Pearson Chi-Square, Fisher’s exact, t-test, and Mann–Whitney tests. Cutoff values were determined using ROC curves, and correlation with survival was examined by Kaplan–Meier method and Cox regression. Results: Patients with NMR<12.62 had a longer PFS compared to patients with higher NMR values (12.0 vs. 10.0 months, p = 0.054) and a significantly longer OS (20.0 vs. 11.0 months, p = 0.010). The same parameter was confirmed as a predictors of favorable response in the patient subgroup with activating EGFR mutations. Patients with NLR>2.9 and LMR<2.5 more often presented with paronichia and diarrhea, and patients with PLR>190 more often had paronichia, diarrhea and hyperbilirubinemia.Conclusion: Low baseline value of the hematological parameter NMR has shown potential as a routine, low-cost, and minimally invasive predictor of survival in EGFR-TKI-treated NSCLC patients.

Notes

This study was supported by the Ministry of Education and Science of the Republic of Serbia [Agreement No.451-03-9/2021-14/200043]. JS and MC are supported by the Science Fund of the Republic of Serbia [PROMIS TRACEPIGEN project No. 6060876]

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33606592 (PMID)
Is part of
1473-7140 (ISSN)