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Molecular risk factors for locoregional recurrence in resected non‐small cell lung cancer

BACKGROUND: Locoregional recurrence is of high risk and is associated with a poor prognosis in terms of OS for non‐small cell lung cancer (NSCLC). Local control is essential for radical cure of NSCLC. Previous studies have investigated the clinicopathological risk factors for locoregional recurrence...

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Autores principales: Guo, Wei, Zhang, Tao, Li, Runze, Chen, Xiaoxi, Pang, Jiaohui, Bao, Hua, Wu, Xue, Shao, Yang, Qiu, Bin, Gao, Shugeng, He, Jie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10417202/
https://www.ncbi.nlm.nih.gov/pubmed/37248810
http://dx.doi.org/10.1002/cam4.6165
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author Guo, Wei
Zhang, Tao
Li, Runze
Chen, Xiaoxi
Pang, Jiaohui
Bao, Hua
Wu, Xue
Shao, Yang
Qiu, Bin
Gao, Shugeng
He, Jie
author_facet Guo, Wei
Zhang, Tao
Li, Runze
Chen, Xiaoxi
Pang, Jiaohui
Bao, Hua
Wu, Xue
Shao, Yang
Qiu, Bin
Gao, Shugeng
He, Jie
author_sort Guo, Wei
collection PubMed
description BACKGROUND: Locoregional recurrence is of high risk and is associated with a poor prognosis in terms of OS for non‐small cell lung cancer (NSCLC). Local control is essential for radical cure of NSCLC. Previous studies have investigated the clinicopathological risk factors for locoregional recurrence, but the genomic biomarkers associated with locoregional recurrence have been inadequately studied. METHODS: A total of 118 patients who underwent tumor resection with mutation‐detected tumor specimens were included. Tumor samples at surgery and pretreatment/postoperative blood samples were collected for mutational profiling. RESULTS: Among 48 patients with disease recurrence, 46% developed locoregional recurrence (LR) and 75% developed distant metastasis (DM). The 3‐year actuarial risk of LR and DM was 25% and 43%, respectively. The first sites of failure were locoregional only (29%), locoregional and distant (10%), and distant only (61%). Patients with LR showed significantly higher ctDNA level than those with only DM at the time of initial recurrence. On multivariate analysis of baseline risk factors, the presence of allele frequency heterogeneity and baseline ctDNA shedding were found to be independently associated with a higher risk of LR. Patients with disruptive TP53 mutations had significantly lower LR‐free survival as compared to patients with wild‐type TP53 or nondisruptive mutations. EGFR mutations showed a favorable prognostic value for LR and is not induced by EGFR tyrosine kinase inhibitor therapy. Both disruptive TP53 mutation and EGFR mutation remained the significant prognostic factor after adjustment for histological type, pathologic nodal stage and adjuvant therapy. CONCLUSIONS: Nearly half of disease recurrences after surgery for NSCC involved locoregional sites. We identified genomic biomarkers from baseline tumor and ctDNA samples which showed promising prognostic value for LR only. This can help identify patients who had a higher risk of locoregional recurrence regardless of the risk of distant metastasis.
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spelling pubmed-104172022023-08-12 Molecular risk factors for locoregional recurrence in resected non‐small cell lung cancer Guo, Wei Zhang, Tao Li, Runze Chen, Xiaoxi Pang, Jiaohui Bao, Hua Wu, Xue Shao, Yang Qiu, Bin Gao, Shugeng He, Jie Cancer Med RESEARCH ARTICLES BACKGROUND: Locoregional recurrence is of high risk and is associated with a poor prognosis in terms of OS for non‐small cell lung cancer (NSCLC). Local control is essential for radical cure of NSCLC. Previous studies have investigated the clinicopathological risk factors for locoregional recurrence, but the genomic biomarkers associated with locoregional recurrence have been inadequately studied. METHODS: A total of 118 patients who underwent tumor resection with mutation‐detected tumor specimens were included. Tumor samples at surgery and pretreatment/postoperative blood samples were collected for mutational profiling. RESULTS: Among 48 patients with disease recurrence, 46% developed locoregional recurrence (LR) and 75% developed distant metastasis (DM). The 3‐year actuarial risk of LR and DM was 25% and 43%, respectively. The first sites of failure were locoregional only (29%), locoregional and distant (10%), and distant only (61%). Patients with LR showed significantly higher ctDNA level than those with only DM at the time of initial recurrence. On multivariate analysis of baseline risk factors, the presence of allele frequency heterogeneity and baseline ctDNA shedding were found to be independently associated with a higher risk of LR. Patients with disruptive TP53 mutations had significantly lower LR‐free survival as compared to patients with wild‐type TP53 or nondisruptive mutations. EGFR mutations showed a favorable prognostic value for LR and is not induced by EGFR tyrosine kinase inhibitor therapy. Both disruptive TP53 mutation and EGFR mutation remained the significant prognostic factor after adjustment for histological type, pathologic nodal stage and adjuvant therapy. CONCLUSIONS: Nearly half of disease recurrences after surgery for NSCC involved locoregional sites. We identified genomic biomarkers from baseline tumor and ctDNA samples which showed promising prognostic value for LR only. This can help identify patients who had a higher risk of locoregional recurrence regardless of the risk of distant metastasis. John Wiley and Sons Inc. 2023-05-29 /pmc/articles/PMC10417202/ /pubmed/37248810 http://dx.doi.org/10.1002/cam4.6165 Text en © 2023 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle RESEARCH ARTICLES
Guo, Wei
Zhang, Tao
Li, Runze
Chen, Xiaoxi
Pang, Jiaohui
Bao, Hua
Wu, Xue
Shao, Yang
Qiu, Bin
Gao, Shugeng
He, Jie
Molecular risk factors for locoregional recurrence in resected non‐small cell lung cancer
title Molecular risk factors for locoregional recurrence in resected non‐small cell lung cancer
title_full Molecular risk factors for locoregional recurrence in resected non‐small cell lung cancer
title_fullStr Molecular risk factors for locoregional recurrence in resected non‐small cell lung cancer
title_full_unstemmed Molecular risk factors for locoregional recurrence in resected non‐small cell lung cancer
title_short Molecular risk factors for locoregional recurrence in resected non‐small cell lung cancer
title_sort molecular risk factors for locoregional recurrence in resected non‐small cell lung cancer
topic RESEARCH ARTICLES
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10417202/
https://www.ncbi.nlm.nih.gov/pubmed/37248810
http://dx.doi.org/10.1002/cam4.6165
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