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Metachronous Brain Metastasis in patients with EGFR-mutant NSCLC indicates a worse prognosis
Purpose: NSCLC patients with EGFR mutation were associated with high incidence of brain metastasis (BM). BM could be grouped by the time of occurrence, including synchronous BM at initial diagnosis and metachronous BM during disease course. The primary aim of the study was to investigate the surviva...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Ivyspring International Publisher
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7646168/ https://www.ncbi.nlm.nih.gov/pubmed/33193892 http://dx.doi.org/10.7150/jca.46462 |
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author | Ouyang, Wen Yu, Jing zhou, Yan Xu, Yu Li, Jie Gong, Jun Zhang, Junhong Xie, Conghua |
author_facet | Ouyang, Wen Yu, Jing zhou, Yan Xu, Yu Li, Jie Gong, Jun Zhang, Junhong Xie, Conghua |
author_sort | Ouyang, Wen |
collection | PubMed |
description | Purpose: NSCLC patients with EGFR mutation were associated with high incidence of brain metastasis (BM). BM could be grouped by the time of occurrence, including synchronous BM at initial diagnosis and metachronous BM during disease course. The primary aim of the study was to investigate the survival of patients with metachronous BM. Methods: A total of 99 EGFR-mutant advanced NSCLC patients in our institute between 2012 and 2018 were grouped into synchronous BM and metachronous BM. Comparisons of OS were performed based on BM status. The independent prognostic factors of OS were investigated, and extracranial and intracranial PFS were further analyzed. Results: Patients with metachronous BM (mOS: 22.1 months) had poorer outcomes than synchronous BM (mOS: 30.3 months) (P=0.016). Moreover, multivariate analysis indicated that BM status (P=0.015), local therapy for BM (P=0.013) and subsequent treatment of Osimertinib (P=0.008) impact significantly on OS. Significantly, the proportion of local therapy for BM had no difference between patients with synchronous and metachronous BM. And patients with metachronous BM harbored a more favorable prognostic factor (higher proportion of subsequent Osimertinib treatment), but also harbored a poorer prognostic factor (metachronous BM), which confirmed BM status was the most significant prognostic factor of OS. At last, results of extracranial and intracranial PFS indicated that patients with metachronous BM tended to have a higher risk of intracranial disease progression. Conclusions: Patients developing metachronous BM during EGFR-TKIs treatment have worse outcomes than synchronous BM. Our findings suggested that the patients with metachronous BM should receive more aggressive treatments. |
format | Online Article Text |
id | pubmed-7646168 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Ivyspring International Publisher |
record_format | MEDLINE/PubMed |
spelling | pubmed-76461682020-11-12 Metachronous Brain Metastasis in patients with EGFR-mutant NSCLC indicates a worse prognosis Ouyang, Wen Yu, Jing zhou, Yan Xu, Yu Li, Jie Gong, Jun Zhang, Junhong Xie, Conghua J Cancer Research Paper Purpose: NSCLC patients with EGFR mutation were associated with high incidence of brain metastasis (BM). BM could be grouped by the time of occurrence, including synchronous BM at initial diagnosis and metachronous BM during disease course. The primary aim of the study was to investigate the survival of patients with metachronous BM. Methods: A total of 99 EGFR-mutant advanced NSCLC patients in our institute between 2012 and 2018 were grouped into synchronous BM and metachronous BM. Comparisons of OS were performed based on BM status. The independent prognostic factors of OS were investigated, and extracranial and intracranial PFS were further analyzed. Results: Patients with metachronous BM (mOS: 22.1 months) had poorer outcomes than synchronous BM (mOS: 30.3 months) (P=0.016). Moreover, multivariate analysis indicated that BM status (P=0.015), local therapy for BM (P=0.013) and subsequent treatment of Osimertinib (P=0.008) impact significantly on OS. Significantly, the proportion of local therapy for BM had no difference between patients with synchronous and metachronous BM. And patients with metachronous BM harbored a more favorable prognostic factor (higher proportion of subsequent Osimertinib treatment), but also harbored a poorer prognostic factor (metachronous BM), which confirmed BM status was the most significant prognostic factor of OS. At last, results of extracranial and intracranial PFS indicated that patients with metachronous BM tended to have a higher risk of intracranial disease progression. Conclusions: Patients developing metachronous BM during EGFR-TKIs treatment have worse outcomes than synchronous BM. Our findings suggested that the patients with metachronous BM should receive more aggressive treatments. Ivyspring International Publisher 2020-10-21 /pmc/articles/PMC7646168/ /pubmed/33193892 http://dx.doi.org/10.7150/jca.46462 Text en © The author(s) This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/). See http://ivyspring.com/terms for full terms and conditions. |
spellingShingle | Research Paper Ouyang, Wen Yu, Jing zhou, Yan Xu, Yu Li, Jie Gong, Jun Zhang, Junhong Xie, Conghua Metachronous Brain Metastasis in patients with EGFR-mutant NSCLC indicates a worse prognosis |
title | Metachronous Brain Metastasis in patients with EGFR-mutant NSCLC indicates a worse prognosis |
title_full | Metachronous Brain Metastasis in patients with EGFR-mutant NSCLC indicates a worse prognosis |
title_fullStr | Metachronous Brain Metastasis in patients with EGFR-mutant NSCLC indicates a worse prognosis |
title_full_unstemmed | Metachronous Brain Metastasis in patients with EGFR-mutant NSCLC indicates a worse prognosis |
title_short | Metachronous Brain Metastasis in patients with EGFR-mutant NSCLC indicates a worse prognosis |
title_sort | metachronous brain metastasis in patients with egfr-mutant nsclc indicates a worse prognosis |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7646168/ https://www.ncbi.nlm.nih.gov/pubmed/33193892 http://dx.doi.org/10.7150/jca.46462 |
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