Efficacy analysis of brain radiotherapy in EGFR mutation non-small cell lung cancer with brain metastasis: a retrospective study.

IF 2.8 4区 医学 Q3 ENDOCRINOLOGY & METABOLISM
Kaicheng Pan, Bing Wang, Xiao Xu, Yi Tang, Jiafeng Liang, Shenglin Ma, Bing Xia, Lucheng Zhu
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Abstract

Objectives: Patients with epidermal growth factor receptor (EGFR)-mutant non-small cell lung cancer (NSCLC) are at a heightened risk of developing brain metastases (BM). EGFR-tyrosine kinase inhibitors (TKI) are standard treatment for EGFR-mutated NSCLC. However, the necessity and optimal approach of brain radiotherapy for NSCLC patients with EGFR mutation remain inconclusive. We aimed to answer these questions by retrospectively analyzing the efficacy of radiotherapy in patients with BM from NSCLC with EGFR mutations.

Methods: Patients with EGFR- mutant NSCLC and BMs who were diagnosed between January 1, 2018 and December 31, 2022 were included. According to treatment methods those patients were divided into whole brain radiotherapy (WBRT) plus EGFR-TKI (WBRT group), stereotactic radiotherapy (SRT) plus EGFR-TKI (SRT group) and EGFR-TKI alone (TKI-only group). Propensity-score-matching (PSM) was performed to minimize the effect of possible confounding factors and to balance treatment groups.

Results: A total of 142 patients were included in this study. The median follow-up time was 22 months (range, 3.0-43.0 months). In the PSM cohort, the median intracranial progression free survival (iPFS) was 14, 30, 12 months and the median overall survival (OS) was 27 months, not reach and 33 months in WBRT group, SRT group and TKI-only group, respectively. Compared with the other two groups, SRT group significantly improved iPFS and OS (p < 0.05). And the local progression rate of intracranial lesions in SRT group was significantly reduced (p < 0.05).

Conclusion: This study showed that SRT combined with TKI may improve iPFS and prolong survival in patients with EGFR mutations in BMs from NSCLC.

脑放疗治疗EGFR突变非小细胞肺癌合并脑转移的疗效分析:回顾性研究。
研究目的表皮生长因子受体(EGFR)突变型非小细胞肺癌(NSCLC)患者发生脑转移(BM)的风险较高。表皮生长因子受体酪氨酸激酶抑制剂(TKI)是治疗表皮生长因子受体突变非小细胞肺癌的标准疗法。然而,对于表皮生长因子受体(EGFR)突变的NSCLC患者,脑放疗的必要性和最佳方法仍无定论。我们旨在通过回顾性分析表皮生长因子受体(EGFR)突变的NSCLC患者脑部放疗的疗效来回答这些问题:纳入2018年1月1日至2022年12月31日期间确诊的EGFR突变NSCLC和BM患者。根据治疗方法,这些患者被分为全脑放疗(WBRT)加EGFR-TKI(WBRT组)、立体定向放疗(SRT)加EGFR-TKI(SRT组)和单纯EGFR-TKI(单纯TKI组)。为了最大限度地减少可能的混杂因素的影响并平衡治疗组,进行了倾向分数匹配(PSM):本研究共纳入了 142 例患者。中位随访时间为 22 个月(3.0-43.0 个月)。在 PSM 队列中,WBRT 组、SRT 组和纯 TKI 组的中位颅内无进展生存期(iPFS)分别为 14 个月、30 个月、12 个月,中位总生存期(OS)分别为 27 个月、未达到和 33 个月。与其他两组相比,SRT 组的 iPFS 和 OS 均有明显改善(p 结论:SRT 组的 iPFS 和 OS 均有明显改善(p):本研究表明,SRT 联合 TKI 可改善 NSCLC 表皮生长因子受体(EGFR)突变患者的 iPFS 并延长生存期。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Discover. Oncology
Discover. Oncology Medicine-Endocrinology, Diabetes and Metabolism
CiteScore
2.40
自引率
9.10%
发文量
122
审稿时长
5 weeks
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