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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...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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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. |
format | Online Article Text |
id | pubmed-8763652 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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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