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首页> 外文期刊>Cancer science. >First-line epidermal growth factor receptor (EGFR)-tyrosine kinase inhibitor alone or with whole-brain radiotherapy for brain metastases in patients with EGFR-mutated lung adenocarcinoma
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First-line epidermal growth factor receptor (EGFR)-tyrosine kinase inhibitor alone or with whole-brain radiotherapy for brain metastases in patients with EGFR-mutated lung adenocarcinoma

机译:一线表皮生长因子受体(EGFR)-酪氨酸激酶抑制剂单独或与全脑放疗一起用于EGFR突变的肺腺癌患者的脑转移

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摘要

We proposed to compare the outcomes of first-line epidermal growth factor receptor-tyrosine kinase inhibitor (EGFR-TKI) alone with EGFR-TKI plus whole-brain radiotherapy (WBRT) for the treatment of brain metastases (BM) in patients with EGFR-mutated lung adenocarcinoma. A total of 1665 patients were screened from 2008 to 2014, and 132 were enrolled in our study. Among the 132 patients, 72 (54.5%) harbored a deletion in exon 19, 97 (73.5%) showed multiple intracranial lesions, and 67 (50.8%) had asymptomatic BM. Seventy-nine patients (59.8%) were treated with EGFR-TKI alone, 53 with concomitant WBRT. The intracranial objective response rate was significantly higher in the EGFR-TKI plus WBRT treatment group (67.9%) compared with the EGFR-TKI alone group (39.2%) (P = 0.001). After a median follow-up of 36.2 months, 62.1% of patients were still alive. The median intracranial TTP was 24.7 months (95% CI, 19.5-29.9) in patients who received WBRT, which was significantly longer than in those who received EGFR-TKI alone, with the median intracranial TTP of 18.2 months (95% CI, 12.5-23.9) (P = 0.004). There was no significant difference in overall survival between WBRT and EGFR-TKI alone groups, (median, 48.0 vs 41.1 months; P = 0.740). The overall survival is significantly prolonged in patients who had an intracranial TTP exceeding 22 months compared to those who developed intracranial progression <22 months after treatment, (median, 58.0 vs 28.0 months; P = 0.001). For EGFR-mutated lung adenocarcinoma patients with BM, treatment with concomitant WBRT achieved a higher response rate of BM and significant improvement in intracranial progression-free survival compared with EGFR-TKI alone.
机译:我们提议比较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)治疗EGFR-T细胞脑转移(BM)的结果突变的肺腺癌。从2008年到2014年,共筛查了1665例患者,其中132例纳入了我们的研究。在132例患者中,有72例(54.5%)的第19外显子缺失,其中97例(73.5%)显示出颅内多处病变,而67例(50.8%)则无症状。仅使用EGFR-TKI治疗了79例患者(59.8%),同时进行了WBRT治疗53例。与单独使用EGFR-TKI的组(39.2%)相比,EGFR-TKI加WBRT治疗组的颅内客观反应率(67.9%)显着更高(P = 0.001)。在中位随访36.2个月之后,仍有62.1%的患者还活着。接受WBRT的患者的颅内TTP的中位数为24.7个月(95%CI,19.5-29.9),这比仅接受EGFR-TKI的患者长得多,颅内TTP的中位数为18.2个月(95%CI,12.5) -23.9)(P = 0.004)。单独使用WBRT组和EGFR-TKI组的总生存期无显着差异(中位值分别为48.0和41.1个月; P = 0.740)。颅内TTP超过22个月的患者与治疗后<22个月颅内进展的患者相比,总生存期显着延长(中位数为58.0 vs 28.0个月; P = 0.001)。对于EGFR突变的BM肺腺癌患者,与单独的EGFR-TKI相比,同时进行WBRT治疗可实现更高的BM反应率,并显着改善颅内无进展生存期。

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