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Anlotinib combined with whole-brain radiotherapy in non-small cell lung cancer with multiple brain metastases that progressed or developed after at least one lines of prior treatment

BACKGROUND: Intracranial metastasis that failed standard systematic treatment is common in advanced non-small cell lung cancer (NSCLC), contributing significantly to morbidity and mortality. The aim of this study was to evaluate the efficacy and safety of anlotinib combined with whole-brain radiothe...

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Autores principales: Kong, Cheng, Yu, Shaorong, Qian, Pudong, Song, Xue, Wen, Jing, Jiang, Ming, Zhu, Jun, Xu, Jianhua, Zhao, Lijun, Guo, Zhen, Wu, Jianfeng, He, Xia, Zhu, Xiangzhi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10523148/
https://www.ncbi.nlm.nih.gov/pubmed/37771446
http://dx.doi.org/10.3389/fonc.2023.1169333
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author Kong, Cheng
Yu, Shaorong
Qian, Pudong
Song, Xue
Wen, Jing
Jiang, Ming
Zhu, Jun
Xu, Jianhua
Zhao, Lijun
Guo, Zhen
Wu, Jianfeng
He, Xia
Zhu, Xiangzhi
author_facet Kong, Cheng
Yu, Shaorong
Qian, Pudong
Song, Xue
Wen, Jing
Jiang, Ming
Zhu, Jun
Xu, Jianhua
Zhao, Lijun
Guo, Zhen
Wu, Jianfeng
He, Xia
Zhu, Xiangzhi
author_sort Kong, Cheng
collection PubMed
description BACKGROUND: Intracranial metastasis that failed standard systematic treatment is common in advanced non-small cell lung cancer (NSCLC), contributing significantly to morbidity and mortality. The aim of this study was to evaluate the efficacy and safety of anlotinib combined with whole-brain radiotherapy (WBRT) for NSCLC with brain metastases (BMs) that progressed or developed after at least one line of prior treatment and compare the outcomes with that of the contemporary institutional control. METHODS: NSCLC patients with multiple BMs that progressed or developed after at least one line of prior systematic treatment and treated with WBRT subsequently between 2019 and 2021 were selected retrospectively for analysis. Based on whether concurrent anlotinib had been used in combination with WBRT, the cases were divided into the anlotinib group and control group. The primary endpoints were intracranial progression-free survival (iPFS) and safety. RESULTS: A total of 76 patients met the inclusion criteria of the study. Of the 76 patients, 34 received concurrent WBRT and anlotinib followed by anlotinib maintenance and 42 were treated with WBRT alone or in combination with other systemic agents at the physicians’ discretion. The median follow-up for the entire cohort was 21 months. The median iPFS for the anlotinib and control group was 6.7 months (95% CI, 4.6–9.9) and 5.3 months (95% CI, 4.0–6.5), respectively (log-rank P = 0.04). There was no difference in overall survival between the two groups (log-rank P = 0.38). In the anlotinib group, treatment-related adverse events were reported in 15 patients (44.1%), with acute or late grade 3–5 adverse events identified in 14.7% of patients (n = 5). CONCLUSIONS: WBRT plus anlotinib, as a convenient chemo-free regimen, may represent an overall safe and effective procedure in advanced NSCLC with multiple BMs that progressed or developed after standard systematic treatment.
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spelling pubmed-105231482023-09-28 Anlotinib combined with whole-brain radiotherapy in non-small cell lung cancer with multiple brain metastases that progressed or developed after at least one lines of prior treatment Kong, Cheng Yu, Shaorong Qian, Pudong Song, Xue Wen, Jing Jiang, Ming Zhu, Jun Xu, Jianhua Zhao, Lijun Guo, Zhen Wu, Jianfeng He, Xia Zhu, Xiangzhi Front Oncol Oncology BACKGROUND: Intracranial metastasis that failed standard systematic treatment is common in advanced non-small cell lung cancer (NSCLC), contributing significantly to morbidity and mortality. The aim of this study was to evaluate the efficacy and safety of anlotinib combined with whole-brain radiotherapy (WBRT) for NSCLC with brain metastases (BMs) that progressed or developed after at least one line of prior treatment and compare the outcomes with that of the contemporary institutional control. METHODS: NSCLC patients with multiple BMs that progressed or developed after at least one line of prior systematic treatment and treated with WBRT subsequently between 2019 and 2021 were selected retrospectively for analysis. Based on whether concurrent anlotinib had been used in combination with WBRT, the cases were divided into the anlotinib group and control group. The primary endpoints were intracranial progression-free survival (iPFS) and safety. RESULTS: A total of 76 patients met the inclusion criteria of the study. Of the 76 patients, 34 received concurrent WBRT and anlotinib followed by anlotinib maintenance and 42 were treated with WBRT alone or in combination with other systemic agents at the physicians’ discretion. The median follow-up for the entire cohort was 21 months. The median iPFS for the anlotinib and control group was 6.7 months (95% CI, 4.6–9.9) and 5.3 months (95% CI, 4.0–6.5), respectively (log-rank P = 0.04). There was no difference in overall survival between the two groups (log-rank P = 0.38). In the anlotinib group, treatment-related adverse events were reported in 15 patients (44.1%), with acute or late grade 3–5 adverse events identified in 14.7% of patients (n = 5). CONCLUSIONS: WBRT plus anlotinib, as a convenient chemo-free regimen, may represent an overall safe and effective procedure in advanced NSCLC with multiple BMs that progressed or developed after standard systematic treatment. Frontiers Media S.A. 2023-09-12 /pmc/articles/PMC10523148/ /pubmed/37771446 http://dx.doi.org/10.3389/fonc.2023.1169333 Text en Copyright © 2023 Kong, Yu, Qian, Song, Wen, Jiang, Zhu, Xu, Zhao, Guo, Wu, He and Zhu https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Kong, Cheng
Yu, Shaorong
Qian, Pudong
Song, Xue
Wen, Jing
Jiang, Ming
Zhu, Jun
Xu, Jianhua
Zhao, Lijun
Guo, Zhen
Wu, Jianfeng
He, Xia
Zhu, Xiangzhi
Anlotinib combined with whole-brain radiotherapy in non-small cell lung cancer with multiple brain metastases that progressed or developed after at least one lines of prior treatment
title Anlotinib combined with whole-brain radiotherapy in non-small cell lung cancer with multiple brain metastases that progressed or developed after at least one lines of prior treatment
title_full Anlotinib combined with whole-brain radiotherapy in non-small cell lung cancer with multiple brain metastases that progressed or developed after at least one lines of prior treatment
title_fullStr Anlotinib combined with whole-brain radiotherapy in non-small cell lung cancer with multiple brain metastases that progressed or developed after at least one lines of prior treatment
title_full_unstemmed Anlotinib combined with whole-brain radiotherapy in non-small cell lung cancer with multiple brain metastases that progressed or developed after at least one lines of prior treatment
title_short Anlotinib combined with whole-brain radiotherapy in non-small cell lung cancer with multiple brain metastases that progressed or developed after at least one lines of prior treatment
title_sort anlotinib combined with whole-brain radiotherapy in non-small cell lung cancer with multiple brain metastases that progressed or developed after at least one lines of prior treatment
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10523148/
https://www.ncbi.nlm.nih.gov/pubmed/37771446
http://dx.doi.org/10.3389/fonc.2023.1169333
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