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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...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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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. |
format | Online Article Text |
id | pubmed-10417202 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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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