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Circulating Tumor DNA as a Prognostic Biomarker in Localized Non-small Cell Lung Cancer

BACKGROUND: Routine clinical surveillance involves serial radiographic imaging following radical surgery in localized non-small cell lung cancer (NSCLC). However, such surveillance can detect only macroscopic disease recurrence and is frequently inconclusive. We investigated if detection of ctDNA be...

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Autores principales: Peng, Muyun, Huang, Qi, Yin, Wei, Tan, Sichuang, Chen, Chen, Liu, Wenliang, Tang, Jingqun, Wang, Xiang, Zhang, Bingyu, Zou, Min, Li, Jina, Su, Wenhui, Wang, Lientu, Chin, Lihan, Yu, Fenglei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7523087/
https://www.ncbi.nlm.nih.gov/pubmed/33042842
http://dx.doi.org/10.3389/fonc.2020.561598
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author Peng, Muyun
Huang, Qi
Yin, Wei
Tan, Sichuang
Chen, Chen
Liu, Wenliang
Tang, Jingqun
Wang, Xiang
Zhang, Bingyu
Zou, Min
Li, Jina
Su, Wenhui
Wang, Lientu
Chin, Lihan
Yu, Fenglei
author_facet Peng, Muyun
Huang, Qi
Yin, Wei
Tan, Sichuang
Chen, Chen
Liu, Wenliang
Tang, Jingqun
Wang, Xiang
Zhang, Bingyu
Zou, Min
Li, Jina
Su, Wenhui
Wang, Lientu
Chin, Lihan
Yu, Fenglei
author_sort Peng, Muyun
collection PubMed
description BACKGROUND: Routine clinical surveillance involves serial radiographic imaging following radical surgery in localized non-small cell lung cancer (NSCLC). However, such surveillance can detect only macroscopic disease recurrence and is frequently inconclusive. We investigated if detection of ctDNA before and after resection of NSCLC identifies the patients with risk of relapse, and furthermore, informs about response to management. METHODS: We recruited a total of 77 NSCLC patients. A high-throughput 127 target-gene capture technology and a high-sensitivity circulating single-molecule amplification and resequencing technology (cSMART) assay were used to detect the somatic mutations in the tumor tissues as well as the plasma of NSCLC patients before and after surgery to monitor for minimal residual disease (MRD). Kaplan-Meier and Cox regression analysis were performed to evaluate the relapse-free survival (RFS) and overall survival (OS) of patients with predictor variables. RESULTS: Patients with a higher stage (III/IV) and preoperative ctDNA-positive status demonstrated a significant 2.8-3.4-fold risk and 3.8-4.0-fold risk for recurrence and death, respectively. Preoperative ctDNA-positive patients associated with a lower RFS (HR = 3.812, p = 0.0005) and OS (HR = 5.004, p = 0.0009). Postoperative ctDNA-positive patients also associated with a lower RFS (HR = 3.076, p = 0.0015) and OS (HR = 3.195, p = 0.0053). Disease recurrence occurred among 63.3% (19/30) of postoperative ctDNA-positive patients. Most of these patients 89.5% (17/19) had detectable ctDNA within 2 weeks after surgery and was identified in advance of radiographic findings by a median of 12.6 months. CONCLUSION: Advanced stage and preoperative ctDNA-positive are strong predictors of RFS and OS in localized NSCLC patients undergoing complete resection. Postoperative detection of ctDNA increases chance to detect early relapse, thus can fulfill an important role in stratifying patients for immediate further treatment with adjuvant and neoadjuvant therapy.
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spelling pubmed-75230872020-10-09 Circulating Tumor DNA as a Prognostic Biomarker in Localized Non-small Cell Lung Cancer Peng, Muyun Huang, Qi Yin, Wei Tan, Sichuang Chen, Chen Liu, Wenliang Tang, Jingqun Wang, Xiang Zhang, Bingyu Zou, Min Li, Jina Su, Wenhui Wang, Lientu Chin, Lihan Yu, Fenglei Front Oncol Oncology BACKGROUND: Routine clinical surveillance involves serial radiographic imaging following radical surgery in localized non-small cell lung cancer (NSCLC). However, such surveillance can detect only macroscopic disease recurrence and is frequently inconclusive. We investigated if detection of ctDNA before and after resection of NSCLC identifies the patients with risk of relapse, and furthermore, informs about response to management. METHODS: We recruited a total of 77 NSCLC patients. A high-throughput 127 target-gene capture technology and a high-sensitivity circulating single-molecule amplification and resequencing technology (cSMART) assay were used to detect the somatic mutations in the tumor tissues as well as the plasma of NSCLC patients before and after surgery to monitor for minimal residual disease (MRD). Kaplan-Meier and Cox regression analysis were performed to evaluate the relapse-free survival (RFS) and overall survival (OS) of patients with predictor variables. RESULTS: Patients with a higher stage (III/IV) and preoperative ctDNA-positive status demonstrated a significant 2.8-3.4-fold risk and 3.8-4.0-fold risk for recurrence and death, respectively. Preoperative ctDNA-positive patients associated with a lower RFS (HR = 3.812, p = 0.0005) and OS (HR = 5.004, p = 0.0009). Postoperative ctDNA-positive patients also associated with a lower RFS (HR = 3.076, p = 0.0015) and OS (HR = 3.195, p = 0.0053). Disease recurrence occurred among 63.3% (19/30) of postoperative ctDNA-positive patients. Most of these patients 89.5% (17/19) had detectable ctDNA within 2 weeks after surgery and was identified in advance of radiographic findings by a median of 12.6 months. CONCLUSION: Advanced stage and preoperative ctDNA-positive are strong predictors of RFS and OS in localized NSCLC patients undergoing complete resection. Postoperative detection of ctDNA increases chance to detect early relapse, thus can fulfill an important role in stratifying patients for immediate further treatment with adjuvant and neoadjuvant therapy. Frontiers Media S.A. 2020-09-15 /pmc/articles/PMC7523087/ /pubmed/33042842 http://dx.doi.org/10.3389/fonc.2020.561598 Text en Copyright © 2020 Peng, Huang, Yin, Tan, Chen, Liu, Tang, Wang, Zhang, Zou, Li, Su, Wang, Chin and Yu. http://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
Peng, Muyun
Huang, Qi
Yin, Wei
Tan, Sichuang
Chen, Chen
Liu, Wenliang
Tang, Jingqun
Wang, Xiang
Zhang, Bingyu
Zou, Min
Li, Jina
Su, Wenhui
Wang, Lientu
Chin, Lihan
Yu, Fenglei
Circulating Tumor DNA as a Prognostic Biomarker in Localized Non-small Cell Lung Cancer
title Circulating Tumor DNA as a Prognostic Biomarker in Localized Non-small Cell Lung Cancer
title_full Circulating Tumor DNA as a Prognostic Biomarker in Localized Non-small Cell Lung Cancer
title_fullStr Circulating Tumor DNA as a Prognostic Biomarker in Localized Non-small Cell Lung Cancer
title_full_unstemmed Circulating Tumor DNA as a Prognostic Biomarker in Localized Non-small Cell Lung Cancer
title_short Circulating Tumor DNA as a Prognostic Biomarker in Localized Non-small Cell Lung Cancer
title_sort circulating tumor dna as a prognostic biomarker in localized non-small cell lung cancer
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7523087/
https://www.ncbi.nlm.nih.gov/pubmed/33042842
http://dx.doi.org/10.3389/fonc.2020.561598
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