The Efficacy of Anlotinib Plus Whole Brain Radiotherapy in Advanced Non-Small Cell Lung Cancer With Multiple Brain Metastases: A Retrospective Study

被引:0
作者
Liu, Lipin [1 ]
Xu, Yonggang [1 ]
Gao, Hong [1 ]
Zhao, Ting [1 ]
Chen, Dazhi [1 ]
Jin, Jingyi [1 ]
Gao, Cui [1 ]
Li, Gaofeng [1 ]
Zhong, Qiuzi [1 ]
机构
[1] Chinese Acad Med Sci, Beijing Hosp, Natl Ctr Gerontol, Dept Radiat Oncol,Inst Geriatr Med, Beijing, Peoples R China
关键词
anlotinib; brain metastases; non-small cell lung cancer; whole-brain radiotherapy; RADIATION; SURVIVAL; THERAPY; NSCLC; WBRT;
D O I
10.1111/1759-7714.15498
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
PurposeThis study aimed to compare the efficacy of anlotinib plus whole-brain radiotherapy (WBRT) with that of WBRT alone in non-small cell lung cancer (NSCLC) patients with multiple brain metastases (BMs).MethodsThe clinical data of patients with NSCLC and multiple BMs who received WBRT between 2019 and 2022 were collected. The patients were assigned to anlotinib plus WBRT group and WBRT group according to the treatment used.ResultsA total of 64 patients were eligible for analysis; 21 were treated with anlotinib plus WBRT, and 43 were treated with WBRT. The anlotinib plus WBRT group had a greater proportion of patients who were young and had a better performance status and adenocarcinoma histology than did the WBRT group. The median follow-up time was 18.0 months. The median intracranial progression-free survival (iPFS) was significantly longer in the anlotinib plus WBRT group than in the WBRT group (12.9 months vs. 7.4 months, p = 0.004). The median overall survival (OS) was 14.6 months in the anlotinib plus WBRT group and 9.4 months in the WBRT group (p = 0.039). Considering death as a competing risk to intracranial progression, the 1-year cumulative incidence of intracranial progression in the anlotinib plus WBRT group (26.7%) was significantly lower than that in the WBRT group (64.3%) (p = 0.021). There was no significant difference in treatment-related toxicity between the anlotinib plus WBRT group and the WBRT group.ConclusionCompared with WBRT alone, anlotinib plus WBRT might confer superior intracranial PFS for NSCLC patients with multiple BMs without increasing treatment-related toxicity.
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页数:9
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