Suppr超能文献

安罗替尼联合全脑放疗治疗多发脑转移的晚期非小细胞肺癌的疗效:一项回顾性研究

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

作者信息

Liu Lipin, Xu Yonggang, Gao Hong, Zhao Ting, Chen Dazhi, Jin Jingyi, Gao Cui, Li Gaofeng, Zhong Qiuzi

机构信息

Department of Radiation Oncology, Beijing Hospital, National Center of Gerontology, Institute of Geriatric Medicine, Chinese Academy of Medical Sciences, Beijing, P. R. China.

出版信息

Thorac Cancer. 2025 Jan;16(1):e15498. doi: 10.1111/1759-7714.15498. Epub 2024 Dec 5.

Abstract

PURPOSE

This 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).

METHODS

The 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.

RESULTS

A 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.

CONCLUSION

Compared with WBRT alone, anlotinib plus WBRT might confer superior intracranial PFS for NSCLC patients with multiple BMs without increasing treatment-related toxicity.

摘要

目的

本研究旨在比较安罗替尼联合全脑放疗(WBRT)与单纯WBRT对非小细胞肺癌(NSCLC)多发脑转移(BMs)患者的疗效。

方法

收集2019年至2022年间接受WBRT的NSCLC伴多发BMs患者的临床资料。根据治疗方式将患者分为安罗替尼联合WBRT组和WBRT组。

结果

共有64例患者符合分析条件;21例接受安罗替尼联合WBRT治疗,43例接受WBRT治疗。安罗替尼联合WBRT组中年轻患者、体能状态较好患者及腺癌组织学类型患者的比例高于WBRT组。中位随访时间为18.0个月。安罗替尼联合WBRT组的中位颅内无进展生存期(iPFS)显著长于WBRT组(12.9个月对7.4个月,p = 0.004)。安罗替尼联合WBRT组的中位总生存期(OS)为14.6个月,WBRT组为9.4个月(p = 0.039)。将死亡视为颅内进展的竞争风险,安罗替尼联合WBRT组的1年颅内进展累积发生率(26.7%)显著低于WBRT组(64.3%)(p = 0.021)。安罗替尼联合WBRT组与WBRT组在治疗相关毒性方面无显著差异。

结论

与单纯WBRT相比,安罗替尼联合WBRT可能为NSCLC多发BMs患者带来更好的颅内无进展生存期,且不增加治疗相关毒性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d4e4/11729404/c25a1af44b0e/TCA-16-e15498-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验