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表皮生长因子受体突变对接受伽玛刀放射外科治疗的非小细胞肺癌脑转移患者颅内无进展生存期的影响。

The Effect of Epidermal Growth Factor Receptor Mutation on Intracranial Progression-Free Survival of Non-Small Cell Lung Cancer Patients with Brain Metastasis Underwent Gamma Knife Radiosurgery.

作者信息

Yang Seung Hyeon, Kim Hae Yu, Lee Sun Il, Jin Seong Jin

机构信息

Department of Neurosurgery, Haeundae Paik Hospital, Inje University College of Medicine, Busan, Korea.

Department of Neurosurgery, Gamma Knife Center, Haeundae Paik Hospital, Inje University College of Medicine, Busan, Korea.

出版信息

Brain Tumor Res Treat. 2020 Oct;8(2):103-108. doi: 10.14791/btrt.2020.8.e15.

DOI:10.14791/btrt.2020.8.e15
PMID:33118342
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7595855/
Abstract

BACKGROUND

The aim of this study was to survey prognostic factors, particularly those focusing on epidermal growth factor receptor (EGFR) mutations, of patients with non-small cell lung cancer (NSCLC) after Gamma Knife Radiosurgery (GKRS) for metastatic brain tumors.

METHODS

We retrospectively reviewed the medical records of 98 patients with NSCLC who underwent GKRS for brain metastases from August 2010 to July 2017. The primary endpoint was progression-free survival (PFS) of the intracranial disease. We analyzed variables such as age, sex, Karnofsky Performance Status, recursive partitioning analysis (RPA) class, smoking status, primary cancer pathology, EGFR mutations, and time to brain metastases as prognostic factors.

RESULTS

The median overall survival (OS) of the patients was 16 months [95% confidence interval (CI), 13-21 months]. Median systemic PFS and intracranial PFS were 9 months (95% CI, 8-11 months) and 11 months (95% CI, 7-14 months), respectively. Kaplan-Meier survival analysis revealed that the patients with EGFR mutations had longer intracranial PFS than those without EGFR mutation (median intracranial PFS: 19 vs. 10 months with =0.01) while they had no benefits in OS and systemic PFS. Furthermore, the patients harboring adenocarcinoma had longer OS (<0.01) and intracranial PFS (<0.01) and the patients with lower RPA class had longer OS (=0.02) and intracranial PFS (=0.03).

CONCLUSION

EGFR mutations, primary cancer pathology, and RPA class may be proposed as prognostic factors for intracranial PFS in NSCLC patients after GKRS for brain metastasis in this study.

摘要

背景

本研究旨在调查非小细胞肺癌(NSCLC)患者在接受伽玛刀放射外科治疗(GKRS)以治疗转移性脑肿瘤后的预后因素,尤其是那些聚焦于表皮生长因子受体(EGFR)突变的因素。

方法

我们回顾性分析了2010年8月至2017年7月期间接受GKRS治疗脑转移瘤的98例NSCLC患者的病历。主要终点是颅内疾病的无进展生存期(PFS)。我们分析了年龄、性别、卡氏功能状态、递归分区分析(RPA)分级、吸烟状态、原发性癌症病理、EGFR突变以及脑转移时间等变量作为预后因素。

结果

患者的中位总生存期(OS)为16个月[95%置信区间(CI),13 - 21个月]。中位全身PFS和颅内PFS分别为9个月(95% CI,8 - 11个月)和11个月(95% CI,7 - 14个月)。Kaplan-Meier生存分析显示,EGFR突变患者的颅内PFS长于无EGFR突变患者(中位颅内PFS:19个月对10个月,P = 0.01),而在OS和全身PFS方面无获益。此外,腺癌患者的OS(P < 0.01)和颅内PFS(P < 0.01)更长,RPA分级较低的患者OS(P = 0.02)和颅内PFS(P = 0.03)更长。

结论

在本研究中,EGFR突变、原发性癌症病理和RPA分级可被提议作为NSCLC患者接受GKRS治疗脑转移后颅内PFS的预后因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5dae/7595855/ce081c45403e/btrt-8-103-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5dae/7595855/3d2021265d0b/btrt-8-103-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5dae/7595855/ec458d068cdc/btrt-8-103-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5dae/7595855/ce081c45403e/btrt-8-103-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5dae/7595855/3d2021265d0b/btrt-8-103-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5dae/7595855/ec458d068cdc/btrt-8-103-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5dae/7595855/ce081c45403e/btrt-8-103-g003.jpg

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Comparison of the efficacies of first-generation epidermal growth factor receptor tyrosine kinase inhibitors for brain metastasis in patients with advanced non-small-cell lung cancer harboring EGFR mutations.比较第一代表皮生长因子受体酪氨酸激酶抑制剂治疗携带 EGFR 突变的晚期非小细胞肺癌脑转移患者的疗效。
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