Assessing platelet-lymphocyte ratio in EGFR-mutated non-small cell lung cancer patients treated with tyrosine kinase inhibitors: An analysis across TKI generations
- Ryan Cooper 1, Dhruv Ramaswami 2, Jacob Thomas 3, Jorge Nieva 3, Robert Hsu 3
- Ryan Cooper 1, Dhruv Ramaswami 2, Jacob Thomas 3
- 1University of Southern California Keck School of Medicine.
- 2University of Southern California.
- 3USC Norris Comprehensive Cancer Center.
- 0University of Southern California Keck School of Medicine.
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View abstract on PubMed
Summary
This summary is machine-generated.The platelet-lymphocyte ratio (PLR) is a useful prognostic marker for non-small cell lung cancer (NSCLC) patients treated with first or second-generation EGFR tyrosine kinase inhibitors (TKIs). Its prognostic value is less clear with osimertinib treatment.
Area Of Science
- Oncology
- Medical Laboratory Science
Background
- The prognostic utility of laboratory markers, such as the platelet-lymphocyte ratio (PLR), in non-small cell lung cancer (NSCLC) patients with EGFR mutations treated with tyrosine kinase inhibitors (TKIs) requires further investigation.
- The specific role of PLR in patients treated with osimertinib, a third-generation EGFR TKI, remains undetermined.
Purpose Of The Study
- To evaluate the prognostic significance of the platelet-lymphocyte ratio (PLR) in patients with EGFR-mutated NSCLC treated with different generations of TKIs.
- To compare the changes in laboratory markers, including PLR, between patients treated with first/second-generation TKIs and those treated with osimertinib.
Main Methods
- A retrospective analysis of 151 patients with EGFR-mutated NSCLC treated with EGFR TKIs.
- Progression-free survival (PFS) was analyzed using Kaplan-Meier curves stratified by PLR.
- Changes in laboratory markers were analyzed using Mann-Whitney tests and Cox Hazard Regression for multivariate analysis.
Main Results
- Patients treated with first or second-generation TKIs with a PLR ≥ 180 had significantly shorter median PFS (10.5 months) compared to those with PLR < 180 (16.6 months, p = 0.0163).
- Median PFS was comparable between patients treated with osimertinib, irrespective of their PLR.
- Osimertinib treatment led to significant decreases in absolute lymphocyte count and platelets compared to first/second-generation TKIs.
Conclusions
- The prognostic value of PLR is more pronounced in patients treated with first or second-generation EGFR TKIs than with osimertinib.
- Third-generation EGFR TKIs like osimertinib may offer improved efficacy, potentially overcoming the negative prognostic implications of elevated PLR.
- Observed changes in peripheral cell counts suggest TKI generation-dependent alterations in the tumor microenvironment.
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