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Early assessment of circulating tumor DNA after curative‐intent resection predicts tumor recurrence in early‐stage and locally advanced non‐small‐cell lung cancer

Circulating tumor DNA (ctDNA) has demonstrated great potential as a noninvasive biomarker to assess minimal residual disease (MRD) and profile tumor genotypes in patients with non‐small‐cell lung cancer (NSCLC). However, little is known about its dynamics during and after tumor resection, or its pot...

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Autores principales: Waldeck, Silvia, Mitschke, Jan, Wiesemann, Sebastian, Rassner, Michael, Andrieux, Geoffroy, Deuter, Max, Mutter, Jurik, Lüchtenborg, Anne‐Marie, Kottmann, Daniel, Titze, Laurin, Zeisel, Christoph, Jolic, Martina, Philipp, Ulrike, Lassmann, Silke, Bronsert, Peter, Greil, Christine, Rawluk, Justyna, Becker, Heiko, Isbell, Lisa, Müller, Alexandra, Doostkam, Soroush, Passlick, Bernward, Börries, Melanie, Duyster, Justus, Wehrle, Julius, Scherer, Florian, von Bubnoff, Nikolas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8763652/
https://www.ncbi.nlm.nih.gov/pubmed/34653314
http://dx.doi.org/10.1002/1878-0261.13116
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author Waldeck, Silvia
Mitschke, Jan
Wiesemann, Sebastian
Rassner, Michael
Andrieux, Geoffroy
Deuter, Max
Mutter, Jurik
Lüchtenborg, Anne‐Marie
Kottmann, Daniel
Titze, Laurin
Zeisel, Christoph
Jolic, Martina
Philipp, Ulrike
Lassmann, Silke
Bronsert, Peter
Greil, Christine
Rawluk, Justyna
Becker, Heiko
Isbell, Lisa
Müller, Alexandra
Doostkam, Soroush
Passlick, Bernward
Börries, Melanie
Duyster, Justus
Wehrle, Julius
Scherer, Florian
von Bubnoff, Nikolas
author_facet Waldeck, Silvia
Mitschke, Jan
Wiesemann, Sebastian
Rassner, Michael
Andrieux, Geoffroy
Deuter, Max
Mutter, Jurik
Lüchtenborg, Anne‐Marie
Kottmann, Daniel
Titze, Laurin
Zeisel, Christoph
Jolic, Martina
Philipp, Ulrike
Lassmann, Silke
Bronsert, Peter
Greil, Christine
Rawluk, Justyna
Becker, Heiko
Isbell, Lisa
Müller, Alexandra
Doostkam, Soroush
Passlick, Bernward
Börries, Melanie
Duyster, Justus
Wehrle, Julius
Scherer, Florian
von Bubnoff, Nikolas
author_sort Waldeck, Silvia
collection PubMed
description Circulating tumor DNA (ctDNA) has demonstrated great potential as a noninvasive biomarker to assess minimal residual disease (MRD) and profile tumor genotypes in patients with non‐small‐cell lung cancer (NSCLC). However, little is known about its dynamics during and after tumor resection, or its potential for predicting clinical outcomes. Here, we applied a targeted‐capture high‐throughput sequencing approach to profile ctDNA at various disease milestones and assessed its predictive value in patients with early‐stage and locally advanced NSCLC. We prospectively enrolled 33 consecutive patients with stage IA to IIIB NSCLC undergoing curative‐intent tumor resection (median follow‐up: 26.2 months). From 21 patients, we serially collected 96 plasma samples before surgery, during surgery, 1–2 weeks postsurgery, and during follow‐up. Deep next‐generation sequencing using unique molecular identifiers was performed to identify and quantify tumor‐specific mutations in ctDNA. Twelve patients (57%) had detectable mutations in ctDNA before tumor resection. Both ctDNA detection rates and ctDNA concentrations were significantly higher in plasma obtained during surgery compared with presurgical specimens (57% versus 19% ctDNA detection rate, and 12.47 versus 6.64 ng·mL(−1), respectively). Four patients (19%) remained ctDNA‐positive at 1–2 weeks after surgery, with all of them (100%) experiencing disease progression at later time points. In contrast, only 4 out of 12 ctDNA‐negative patients (33%) after surgery experienced relapse during follow‐up. Positive ctDNA in early postoperative plasma samples was associated with shorter progression‐free survival (P = 0.013) and overall survival (P = 0.004). Our findings suggest that, in early‐stage and locally advanced NSCLC, intraoperative plasma sampling results in high ctDNA detection rates and that ctDNA positivity early after resection identifies patients at risk for relapse.
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spelling pubmed-87636522022-01-21 Early assessment of circulating tumor DNA after curative‐intent resection predicts tumor recurrence in early‐stage and locally advanced non‐small‐cell lung cancer Waldeck, Silvia Mitschke, Jan Wiesemann, Sebastian Rassner, Michael Andrieux, Geoffroy Deuter, Max Mutter, Jurik Lüchtenborg, Anne‐Marie Kottmann, Daniel Titze, Laurin Zeisel, Christoph Jolic, Martina Philipp, Ulrike Lassmann, Silke Bronsert, Peter Greil, Christine Rawluk, Justyna Becker, Heiko Isbell, Lisa Müller, Alexandra Doostkam, Soroush Passlick, Bernward Börries, Melanie Duyster, Justus Wehrle, Julius Scherer, Florian von Bubnoff, Nikolas Mol Oncol Research Articles Circulating tumor DNA (ctDNA) has demonstrated great potential as a noninvasive biomarker to assess minimal residual disease (MRD) and profile tumor genotypes in patients with non‐small‐cell lung cancer (NSCLC). However, little is known about its dynamics during and after tumor resection, or its potential for predicting clinical outcomes. Here, we applied a targeted‐capture high‐throughput sequencing approach to profile ctDNA at various disease milestones and assessed its predictive value in patients with early‐stage and locally advanced NSCLC. We prospectively enrolled 33 consecutive patients with stage IA to IIIB NSCLC undergoing curative‐intent tumor resection (median follow‐up: 26.2 months). From 21 patients, we serially collected 96 plasma samples before surgery, during surgery, 1–2 weeks postsurgery, and during follow‐up. Deep next‐generation sequencing using unique molecular identifiers was performed to identify and quantify tumor‐specific mutations in ctDNA. Twelve patients (57%) had detectable mutations in ctDNA before tumor resection. Both ctDNA detection rates and ctDNA concentrations were significantly higher in plasma obtained during surgery compared with presurgical specimens (57% versus 19% ctDNA detection rate, and 12.47 versus 6.64 ng·mL(−1), respectively). Four patients (19%) remained ctDNA‐positive at 1–2 weeks after surgery, with all of them (100%) experiencing disease progression at later time points. In contrast, only 4 out of 12 ctDNA‐negative patients (33%) after surgery experienced relapse during follow‐up. Positive ctDNA in early postoperative plasma samples was associated with shorter progression‐free survival (P = 0.013) and overall survival (P = 0.004). Our findings suggest that, in early‐stage and locally advanced NSCLC, intraoperative plasma sampling results in high ctDNA detection rates and that ctDNA positivity early after resection identifies patients at risk for relapse. John Wiley and Sons Inc. 2021-10-31 2022-01 /pmc/articles/PMC8763652/ /pubmed/34653314 http://dx.doi.org/10.1002/1878-0261.13116 Text en © 2021 The Authors. Molecular Oncology published by John Wiley & Sons Ltd on behalf of Federation of European Biochemical Societies 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
Waldeck, Silvia
Mitschke, Jan
Wiesemann, Sebastian
Rassner, Michael
Andrieux, Geoffroy
Deuter, Max
Mutter, Jurik
Lüchtenborg, Anne‐Marie
Kottmann, Daniel
Titze, Laurin
Zeisel, Christoph
Jolic, Martina
Philipp, Ulrike
Lassmann, Silke
Bronsert, Peter
Greil, Christine
Rawluk, Justyna
Becker, Heiko
Isbell, Lisa
Müller, Alexandra
Doostkam, Soroush
Passlick, Bernward
Börries, Melanie
Duyster, Justus
Wehrle, Julius
Scherer, Florian
von Bubnoff, Nikolas
Early assessment of circulating tumor DNA after curative‐intent resection predicts tumor recurrence in early‐stage and locally advanced non‐small‐cell lung cancer
title Early assessment of circulating tumor DNA after curative‐intent resection predicts tumor recurrence in early‐stage and locally advanced non‐small‐cell lung cancer
title_full Early assessment of circulating tumor DNA after curative‐intent resection predicts tumor recurrence in early‐stage and locally advanced non‐small‐cell lung cancer
title_fullStr Early assessment of circulating tumor DNA after curative‐intent resection predicts tumor recurrence in early‐stage and locally advanced non‐small‐cell lung cancer
title_full_unstemmed Early assessment of circulating tumor DNA after curative‐intent resection predicts tumor recurrence in early‐stage and locally advanced non‐small‐cell lung cancer
title_short Early assessment of circulating tumor DNA after curative‐intent resection predicts tumor recurrence in early‐stage and locally advanced non‐small‐cell lung cancer
title_sort early assessment of circulating tumor dna after curative‐intent resection predicts tumor recurrence in early‐stage and locally advanced non‐small‐cell lung cancer
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8763652/
https://www.ncbi.nlm.nih.gov/pubmed/34653314
http://dx.doi.org/10.1002/1878-0261.13116
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