首页> 外文期刊>当代医学科学(英文) >Therapeutic Effect of First-line Epidermal Growth Factor Receptor Tyrosine Kinase Inhibitor (EGFR-TKI)Combined with Whole Brain Radiotherapy on Patients with EGFR Mutation-positive Lung Adenocarcinoma and Brain Metastases
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Therapeutic Effect of First-line Epidermal Growth Factor Receptor Tyrosine Kinase Inhibitor (EGFR-TKI)Combined with Whole Brain Radiotherapy on Patients with EGFR Mutation-positive Lung Adenocarcinoma and Brain Metastases

机译:一线表皮生长因子受体酪氨酸激酶抑制剂(EGFR-TKI)联合全脑放疗对EGFR突变阳性肺腺癌和脑转移瘤的治疗作用

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This study compared the therapeutic effect of first-line epidermal growth factor receptor tyrosine kinase inhibitor(EGFR-TKI)with that of EGFR-TKI plus whole brain radiotherapy(WBRT)on patients with EGFR mutation-positive lung adenocarcinoma and brain metastases.A total of 139 patients with lung adenocarcinoma and brain metastases treated with first-line EGFR-TK1therapy from September 2008 to December 2017 were enrolled in this study.The study endpoints were intracranial time to progression(TTP)and overall survival(OS).The effects of clinical pathological parameters and EGFR gene status on the study endpoints were compared.The results showed that the intracranial TTP was significantly longer in EGFR-TKI plus WBRT group than in EGFR-TKI group (median 30.0 vs.18.2 months,χ2=10.824,P=0.001),but no significant difference in the OS was noted between the two groups (median 48.0 vs.41.1 months,χ2=0.012, P=0.912).Also,there was no statistically significant difference in the OS between patients treated with early and late radiotherapy (P=0.849)and between those with asymptomatic and those with symptomatic intracranial metastases (P=0.189).The OS and intracranial TTP of patients with intracranial oligometastases (≤3metastatic sites)were not significantly different from those of patients with multiple intracranial metastases (P=0.104 and P=0.357,respectively),and exon 19 and exon 21 mutations didn''''t show significant effects on the OS and intracranial TTP of patients (P=0.418 and P=0.386,respectively).In conclusion,there was no statistically significant difference in the OS between the EGFR-TKI alone group and EGFR-TK1 plus WBRT group.However, simultaneous use of WBRT was found to significantly prolong intracranial TTP and improve cerebral symptoms,and thus EGFR-TKI and WBRT combined may be clinically beneficial for patients with EGFR mutation-positive lung adenocarcinoma and brain metastases.
机译:本研究比较了一线表皮生长因子受体酪氨酸激酶抑制剂(EGFR-TKI)与EGFR-TKI联合全脑放疗(WBRT)对EGFR突变阳性肺腺癌和脑转移患者的治疗效果。自2008年9月至2017年12月,采用EGFR-TK1一线治疗的139例肺腺癌和脑转移患者入选本研究,研究终点为颅内进展时间(TTP)和总生存期(OS)。比较研究终点的临床病理参数和EGFR基因状态。结果显示,EGFR-TKI + WBRT组的颅内TTP明显长于EGFR-TKI组(中位值30.0 vs.18.2个月,χ2= 10.824,P = 0.001),但两组之间的OS差异无统计学意义(中位数48.0 vs.41.1个月,χ2= 0.012,P = 0.912)。此外,患者之间的OS差异也无统计学意义早期和晚期放疗(P = 0.849),无症状者和有症状颅内转移者之间的治疗(P = 0.189)。颅内低转移(≤3个转移部位)患者的OS和颅内TTP与术中无明显差异。多发颅内转移的患者(分别为P = 0.104和P = 0.357),外显子19和外显子21突变对患者的OS和颅内TTP均无明显影响(P = 0.418和P = 0.386,结论:单独使用EGFR-TKI组和EGFR-TK1加WBRT组之间的OS差异无统计学意义。然而,发现同时使用WBRT可以显着延长颅内TTP并改善脑部症状,因此EGFR-TKI和WBRT联合使用对EGFR突变阳性的肺腺癌和脑转移患者可能具有临床益处。

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