评估接受酪氨酸激酶抑制剂治疗的表皮生长因子受体突变的非小细胞肺癌患者的血小板-淋巴细胞比率:跨代酪氨酸激酶抑制剂分析

Assessing platelet-lymphocyte ratio in EGFR-mutated non-small cell lung cancer patients treated with tyrosine kinase inhibitors: An analysis across TKI generations.

作者信息

Cooper Ryan, Ramaswami Dhruv, Thomas Jacob, Nieva Jorge, Hsu Robert

机构信息

University of Southern California Keck School of Medicine.

University of Southern California.

出版信息

Res Sq. 2024 Oct 16:rs.3.rs-4930668. doi: 10.21203/rs.3.rs-4930668/v1.

Abstract

INTRODUCTION

The prognostic utility of laboratory markers in patients with non-small cell lung cancer (NSCLC) harboring mutations treated with tyrosine kinase inhibitors (TKIs) is an ongoing area of research. The utility of the platelet-lymphocyte ratio (PLR) in patients treated with osimertinib is undetermined.

METHODS

151 patients treated with TKIs in Los Angeles were grouped into one of two groups according to generation of TKI. Differences in progression free survival (PFS) by stratification by PLR was determined using Kaplan-Meier analysis. Differences in median change in laboratory markers by generation of TKI was analyzed using Mann-Whitney tests. Cox Hazard Regression was used to perform multivariate analysis.

RESULTS

Median PFS of those managed with 1st or 2nd generation TKIs was significantly lower in patients with a PLR ≥ 180 (10.5 months) compared to those with PLR < 180 (16.6 months, p = 0.0163). Median PFS was comparable in those treated with osimertinib regardless of PLR. Patients managed with osimertinib had a significant decrease in absolute lymphocyte count (ALC) at 6 weeks and in platelets at 6 weeks and 3 months compared to those managed with 1st or 2nd generation TKIs.

DISCUSSION

The prognostic value of PLR was more apparent in patients treated with 1st or 2nd generation TKIs compared to those treated with osimertinib. Third generation TKIs may be more efficacious in treating patients with laboratory findings previously shown to predict poor survival. The significant changes in peripheral cell counts suggest variability tumor microenvironment changes dependent on the generation of TKI received.

摘要

引言

对于携带特定突变且接受酪氨酸激酶抑制剂(TKIs)治疗的非小细胞肺癌(NSCLC)患者,实验室标志物的预后效用是一个正在进行研究的领域。血小板淋巴细胞比率(PLR)在接受奥希替尼治疗的患者中的效用尚未确定。

方法

在洛杉矶接受TKIs治疗的151名患者根据TKIs的代别分为两组。使用Kaplan-Meier分析确定按PLR分层的无进展生存期(PFS)差异。使用Mann-Whitney检验分析按TKIs代别划分的实验室标志物中位数变化差异。使用Cox风险回归进行多变量分析。

结果

与PLR < 180的患者(16.6个月,p = 0.0163)相比,PLR≥180的患者接受第一代或第二代TKIs治疗的中位PFS显著更低(10.5个月)。无论PLR如何,接受奥希替尼治疗的患者中位PFS相当。与接受第一代或第二代TKIs治疗的患者相比,接受奥希替尼治疗的患者在6周时绝对淋巴细胞计数(ALC)以及在6周和3个月时血小板均有显著下降。

讨论

与接受奥希替尼治疗的患者相比,PLR的预后价值在接受第一代或第二代TKIs治疗的患者中更为明显。第三代TKIs在治疗实验室检查结果先前显示预测生存不良的患者时可能更有效。外周血细胞计数的显著变化表明肿瘤微环境变化的可变性取决于所接受的TKIs代别。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/418c/11527260/62d35e32d65a/nihpp-rs4930668v1-f0001.jpg

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