Cargando…

Prognostic analysis of patients with non-small cell lung cancer harboring exon 19 or 21 mutation in the epidermal growth factor gene and brain metastases

BACKGROUND: In 1997, the Radiation Therapy Oncology Group (RTOG) put forward the recursive partitioning analysis classification for the prognosis of brain metastases (BMs), but this system does not take into account the epidermal growth factor receptor (EGFR) mutations. The aim of the study is to as...

Descripción completa

Detalles Bibliográficos
Autores principales: Wang, Jing, Liu, Zhiyan, Pang, Qingsong, Zhang, Tian, Chen, Xi, Er, Puchun, Wang, Yuwen, Wang, Ping, Wang, Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7469092/
https://www.ncbi.nlm.nih.gov/pubmed/32883221
http://dx.doi.org/10.1186/s12885-020-07249-7
_version_ 1783578355847659520
author Wang, Jing
Liu, Zhiyan
Pang, Qingsong
Zhang, Tian
Chen, Xi
Er, Puchun
Wang, Yuwen
Wang, Ping
Wang, Jun
author_facet Wang, Jing
Liu, Zhiyan
Pang, Qingsong
Zhang, Tian
Chen, Xi
Er, Puchun
Wang, Yuwen
Wang, Ping
Wang, Jun
author_sort Wang, Jing
collection PubMed
description BACKGROUND: In 1997, the Radiation Therapy Oncology Group (RTOG) put forward the recursive partitioning analysis classification for the prognosis of brain metastases (BMs), but this system does not take into account the epidermal growth factor receptor (EGFR) mutations. The aim of the study is to assess the prognosis of patients with EGFR-mutated non-small cell lung cancer (NSCLC) and BMs in the era of tyrosine kinase inhibitor (TKI) availability. METHODS: This was a retrospective study of consecutive patients with EGFR-mutated (exon 19 or 21) NSCLC diagnosed between 01/2011 and 12/2014 at the Tianjin Medical University Cancer Institute & Hospital and who were ultimately diagnosed with BMs. The patients were stage I-III at initial presentation and developed BMs as the first progression. Overall survival (OS), OS after BM diagnosis (mOS), intracranial progression-free survival (iPFS), response to treatment, and adverse reactions were analyzed. RESULTS: Median survival was 35 months, and the 1- and 2- year survival rates were 95.6% (108/113) and 74.3% (84/113). The 3-month CR + PR rates of radiotherapy(R), chemotherapy(C), targeted treatment(T), and targeted treatment + radiotherapy(T+R) after BMs were 63.0% (17/27), 26.7% (4/15), 50.0% (7/14), and 89.7% (35/39), respectively. The median survival of the four treatments was 20, 9, 12, and 25 months after BMs, respectively (P = 0.001). Multivariable analysis showed that < 3 BMs (odds ratio (OR) = 3.34, 95% confidence interval (CI): 1.89–5.91, P < 0.001) and treatment after BMs (OR = 0.68, 95%CI: 0.54–0.85, P = 0.001) were independently associated with better prognosis. CONCLUSIONS: The prognosis of patients with NSCLC and EGFR mutation in exon 19 or 21 after BM is associated with the number of brain metastasis and the treatment method. Targeted treatment combined with radiotherapy may have some advantages over other treatments, but further study is warranted to validate the results.
format Online
Article
Text
id pubmed-7469092
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-74690922020-09-03 Prognostic analysis of patients with non-small cell lung cancer harboring exon 19 or 21 mutation in the epidermal growth factor gene and brain metastases Wang, Jing Liu, Zhiyan Pang, Qingsong Zhang, Tian Chen, Xi Er, Puchun Wang, Yuwen Wang, Ping Wang, Jun BMC Cancer Research Article BACKGROUND: In 1997, the Radiation Therapy Oncology Group (RTOG) put forward the recursive partitioning analysis classification for the prognosis of brain metastases (BMs), but this system does not take into account the epidermal growth factor receptor (EGFR) mutations. The aim of the study is to assess the prognosis of patients with EGFR-mutated non-small cell lung cancer (NSCLC) and BMs in the era of tyrosine kinase inhibitor (TKI) availability. METHODS: This was a retrospective study of consecutive patients with EGFR-mutated (exon 19 or 21) NSCLC diagnosed between 01/2011 and 12/2014 at the Tianjin Medical University Cancer Institute & Hospital and who were ultimately diagnosed with BMs. The patients were stage I-III at initial presentation and developed BMs as the first progression. Overall survival (OS), OS after BM diagnosis (mOS), intracranial progression-free survival (iPFS), response to treatment, and adverse reactions were analyzed. RESULTS: Median survival was 35 months, and the 1- and 2- year survival rates were 95.6% (108/113) and 74.3% (84/113). The 3-month CR + PR rates of radiotherapy(R), chemotherapy(C), targeted treatment(T), and targeted treatment + radiotherapy(T+R) after BMs were 63.0% (17/27), 26.7% (4/15), 50.0% (7/14), and 89.7% (35/39), respectively. The median survival of the four treatments was 20, 9, 12, and 25 months after BMs, respectively (P = 0.001). Multivariable analysis showed that < 3 BMs (odds ratio (OR) = 3.34, 95% confidence interval (CI): 1.89–5.91, P < 0.001) and treatment after BMs (OR = 0.68, 95%CI: 0.54–0.85, P = 0.001) were independently associated with better prognosis. CONCLUSIONS: The prognosis of patients with NSCLC and EGFR mutation in exon 19 or 21 after BM is associated with the number of brain metastasis and the treatment method. Targeted treatment combined with radiotherapy may have some advantages over other treatments, but further study is warranted to validate the results. BioMed Central 2020-09-03 /pmc/articles/PMC7469092/ /pubmed/32883221 http://dx.doi.org/10.1186/s12885-020-07249-7 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Wang, Jing
Liu, Zhiyan
Pang, Qingsong
Zhang, Tian
Chen, Xi
Er, Puchun
Wang, Yuwen
Wang, Ping
Wang, Jun
Prognostic analysis of patients with non-small cell lung cancer harboring exon 19 or 21 mutation in the epidermal growth factor gene and brain metastases
title Prognostic analysis of patients with non-small cell lung cancer harboring exon 19 or 21 mutation in the epidermal growth factor gene and brain metastases
title_full Prognostic analysis of patients with non-small cell lung cancer harboring exon 19 or 21 mutation in the epidermal growth factor gene and brain metastases
title_fullStr Prognostic analysis of patients with non-small cell lung cancer harboring exon 19 or 21 mutation in the epidermal growth factor gene and brain metastases
title_full_unstemmed Prognostic analysis of patients with non-small cell lung cancer harboring exon 19 or 21 mutation in the epidermal growth factor gene and brain metastases
title_short Prognostic analysis of patients with non-small cell lung cancer harboring exon 19 or 21 mutation in the epidermal growth factor gene and brain metastases
title_sort prognostic analysis of patients with non-small cell lung cancer harboring exon 19 or 21 mutation in the epidermal growth factor gene and brain metastases
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7469092/
https://www.ncbi.nlm.nih.gov/pubmed/32883221
http://dx.doi.org/10.1186/s12885-020-07249-7
work_keys_str_mv AT wangjing prognosticanalysisofpatientswithnonsmallcelllungcancerharboringexon19or21mutationintheepidermalgrowthfactorgeneandbrainmetastases
AT liuzhiyan prognosticanalysisofpatientswithnonsmallcelllungcancerharboringexon19or21mutationintheepidermalgrowthfactorgeneandbrainmetastases
AT pangqingsong prognosticanalysisofpatientswithnonsmallcelllungcancerharboringexon19or21mutationintheepidermalgrowthfactorgeneandbrainmetastases
AT zhangtian prognosticanalysisofpatientswithnonsmallcelllungcancerharboringexon19or21mutationintheepidermalgrowthfactorgeneandbrainmetastases
AT chenxi prognosticanalysisofpatientswithnonsmallcelllungcancerharboringexon19or21mutationintheepidermalgrowthfactorgeneandbrainmetastases
AT erpuchun prognosticanalysisofpatientswithnonsmallcelllungcancerharboringexon19or21mutationintheepidermalgrowthfactorgeneandbrainmetastases
AT wangyuwen prognosticanalysisofpatientswithnonsmallcelllungcancerharboringexon19or21mutationintheepidermalgrowthfactorgeneandbrainmetastases
AT wangping prognosticanalysisofpatientswithnonsmallcelllungcancerharboringexon19or21mutationintheepidermalgrowthfactorgeneandbrainmetastases
AT wangjun prognosticanalysisofpatientswithnonsmallcelllungcancerharboringexon19or21mutationintheepidermalgrowthfactorgeneandbrainmetastases