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表皮生长因子受体突变的非小细胞肺癌一线表皮生长因子受体-酪氨酸激酶抑制剂治疗后恶化部位的聚类分析

Cluster analysis of deterioration sites after first-line epidermal growth factor receptor-tyrosine kinase inhibitor in epidermal growth factor receptor mutated non-small cell lung cancer.

作者信息

Okauchi Shinichiro, Miyazaki Kunihiko, Satoh Hiroaki

机构信息

Mito Medical Center, University of Tsukuba, Tsukuba, Japan.

Ryugasaki Saiseikai Hospital, Ryugasaki, Japan.

出版信息

Contemp Oncol (Pozn). 2022;26(2):123-127. doi: 10.5114/wo.2022.118195. Epub 2022 Jun 30.

Abstract

INTRODUCTION

For epidermal growth factor receptor (EGFR) mutated non-small cell lung cancer (NSCLC), no studies have treated the site of recurrence after first-line tyrosine kinase inhibitor (TKI) treatment as a "metastasis pattern". This study aims to assess whether these patients have a specific "metastasis pattern" at the site of recurrence after the treatment.

MATERIAL AND METHODS

Data were collected from all consecutive EGFR mutated NSCLC patients between 2009 and 2021. Metastatic patterns were analyzed using cluster analysis in patients with EGFR mutated NSCLC.

RESULTS

During the study period, 83 EGFR mutated NSCLC patients were treated with EGFR-TKI. Patients who had no metastases at the time of diagnosis were divided into two groups according to the presence or absence of recurrence of metastases after TKI administration. Patients with metastases at diagnosis were divided into 4 groups by cluster analysis. A statistically significant difference in metastasis frequency was confirmed among these 6 groups (χ test, = 0.0001). Furthermore, when the frequency of metastasis recurrence after TKI administration in these 6 groups was examined, a statistically significant difference was confirmed (χ test, = 0.0001).

CONCLUSIONS

Even in EGFR mutation-positive patients, the knowledge of the recurrent patterns might be useful for clinical practice in the foreseeable future, as it enables more efficient detection of metastatic disease through imaging, and more effective treatment at predicted metastatic sites.

摘要

引言

对于表皮生长因子受体(EGFR)突变的非小细胞肺癌(NSCLC),尚无研究将一线酪氨酸激酶抑制剂(TKI)治疗后的复发部位视为一种“转移模式”。本研究旨在评估这些患者在治疗后的复发部位是否具有特定的“转移模式”。

材料与方法

收集了2009年至2021年间所有连续的EGFR突变NSCLC患者的数据。对EGFR突变NSCLC患者的转移模式进行聚类分析。

结果

在研究期间,83例EGFR突变NSCLC患者接受了EGFR-TKI治疗。诊断时无转移的患者根据TKI给药后转移复发的有无分为两组。诊断时有转移的患者通过聚类分析分为4组。在这6组中证实转移频率存在统计学显著差异(χ检验,P = 0.0001)。此外,当检查这6组中TKI给药后转移复发的频率时,也证实了统计学显著差异(χ检验,P = 0.0001)。

结论

即使在EGFR突变阳性患者中,复发模式的知识在可预见的未来可能对临床实践有用,因为它能够通过影像学更有效地检测转移性疾病,并在预测的转移部位进行更有效的治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf08/9319187/10f968da8559/WO-26-47512-g001.jpg

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