山西医科大学学报2024,Vol.55Issue(1) :24-28.DOI:10.13753/j.issn.1007-6611.2024.01.001

晚期非小细胞肺癌患者EGFR-TKI治疗效果及预后分析

Efficacy and prognosis of EGFR-TKI in treatment of patients with advanced non-small cell lung cancer

周淑杰 肖恒 王海东 陈丁莉
山西医科大学学报2024,Vol.55Issue(1) :24-28.DOI:10.13753/j.issn.1007-6611.2024.01.001

晚期非小细胞肺癌患者EGFR-TKI治疗效果及预后分析

Efficacy and prognosis of EGFR-TKI in treatment of patients with advanced non-small cell lung cancer

周淑杰 1肖恒 1王海东 2陈丁莉1
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作者信息

  • 1. 邯郸市中心医院检验科,邯郸 056201
  • 2. 邯郸市中心医院精准医学中心
  • 折叠

摘要

目的 总结冀南地区晚期非小细胞肺癌(non-small cell lung cancer,NSCLC)患者驱动基因突变情况,探讨表皮生长因子受体(epidermal growth factor receptor,EGFR)突变患者采用一代酪氨酸激酶抑制剂(tyrosine kinase inhibitor,TKI)吉非替尼一线治疗的疗效,寻找影响预后的预测因子.方法 收集2021年1月至2021年6月邯郸市中心医院收治的201例晚期NSCLC患者的临床资料,采用二代测序技术(next generation sequencing,NGS)总结驱动基因突变情况;对入组的91例接受吉非替尼靶向治疗的EGFR突变患者进行随访研究,定期收集患者的生存资料,使用Kaplan-Meier方法绘制吉非替尼治疗后不同影响因素下患者的中位无进展生存期(median progression-free survival,mPFS)曲线;Log-rank检验评估生存差异;采用Cox回归建立风险评估模型,分析不同危险因素对吉非替尼靶向治疗疗效及预后的影响.结果201例晚期NSCLC患者中138例(68.66%)至少发生1种基因突变;EGFR突变频率最高[91例(52.6%)],其中EGFR 21号外显子L858R点突变(42.7%)和EGFR 19号外显子缺失(33.6%)占比排名前两位;40例(43.96%)患者为复杂突变.Kaplan-Meier生存分析及Log-rank检验显示EGFR突变中EX19 del、EX21 L858R、少见突变与复杂突变患者mPFS依次为17.0月、13.0月和8.0月,其中EX19 del组mPFS最优,三组差异有统计学意义(P<0.05);无胸腔积液患者mPFS优于恶性胸腔积液患者(17.0月vs 10.0月,P=0.005);Cox回归分析提示EGFR突变类型是影响NSCLC患者mPFS的独立因素(P<0.05).结论EGFR为冀南地区晚期NSCLC患者突变频率较高的基因,驱动基因突变类型可作为独立预测因子判断吉非替尼靶向治疗后患者的生存情况,少见突变和复杂突变患者疗效和预后均较差.

Abstract

Objective To summarize the driver gene mutations in patients with advanced non-small cell lung cancer(NSCLC)in Ji'nan region,investigate the effectiveness of first-line treatment with gefitinib in patients with epidermal growth factor receptor(EGFR)mutation,and identify predictive factors affecting prognosis.Methods Next-generation sequencing(NGS)was used to detect the driver gene mutations in 201 patients with advanced NSCLC admitted to Handan Central Hospital from January to June 2021.A total of 91 patients with EGFR mutations receiving gefitinib-targeted therapy were followed up to collect the survival data.Kaplan-Meier method was used to analyze the median progression-free survival(mPFS)of patients with various factors after treatment with gefitinib.Log-rank test was utilized to evaluate the survival difference.A risk assessment model was developed using Cox regression to analyze the effects of different risk factors on the effectiveness and the prognosis of gefitinib patients.Results Of the 201 patients with advanced NSCLC,138(68.66%)had at least one gene mutation.EGFR was the most common mutation(91 cases,52.6%),mainly EGFR exon 19 deletion(33.6%)and EGFR exon 21 L858R point mutation(42.7%).Forty patients(43.96%)had complex mutations.Kaplan-Meier survival analysis and Log-rank test showed that the mPFS of patients with EX19 del,EX21 L858R mutation,and rare and complex mutation was 17.0,13.0 and 8.0 months,respectively,and the difference between the three groups was statistically significant(P<0.05).The mPFS was higher in patients without pleural effusion than that of patients with pleural effusion(17.0 months vs 10.0 months,P=0.005).Cox regression analysis revealed that the type of EGFR mutation was an independent factor affecting the mPFS of NSCLC patients(P<0.05).Conclusion In patients with advanced NSCLC in Ji'nan region,EGFR is a gene with a high mutation frequency.The type of driver mutation can be used as an independent predictor to evaluate the survival of patients after targeted gefitinib therapy.Patients with rare or complex mutations have a poor prognosis.

关键词

表皮生长因子受体/吉非替尼/基因突变/二代测序/非小细胞肺癌

Key words

epidermal growth factor receptor/gefitinib/gene mutation/next-generation sequencing/non-small cell lung cancer

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基金项目

河北省医学科学研究课题计划项目(20220530)

出版年

2024
山西医科大学学报
山西医科大学

山西医科大学学报

CSTPCD
影响因子:0.931
ISSN:1007-6611
参考文献量12
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