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Prediction of response to systemic treatment by kinetics of circulating tumor DNA in metastatic pancreatic cancer

INTRODUCTION: Pretherapeutic detectable circulating tumor DNA (ctDNA) represents a promising prognostic biomarker for predicting relapse and overall survival in patients with metastatic pancreatic cancer. However, the prognostic value of ctDNA dynamics during treatment has not been studied thus far....

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Autores principales: Kirchweger, Patrick, Kupferthaler, Alexander, Burghofer, Jonathan, Webersinke, Gerald, Jukic, Emina, Schwendinger, Simon, Wundsam, Helwig, Biebl, Matthias, Petzer, Andreas, Rumpold, Holger
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9468369/
https://www.ncbi.nlm.nih.gov/pubmed/36110940
http://dx.doi.org/10.3389/fonc.2022.902177
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author Kirchweger, Patrick
Kupferthaler, Alexander
Burghofer, Jonathan
Webersinke, Gerald
Jukic, Emina
Schwendinger, Simon
Wundsam, Helwig
Biebl, Matthias
Petzer, Andreas
Rumpold, Holger
author_facet Kirchweger, Patrick
Kupferthaler, Alexander
Burghofer, Jonathan
Webersinke, Gerald
Jukic, Emina
Schwendinger, Simon
Wundsam, Helwig
Biebl, Matthias
Petzer, Andreas
Rumpold, Holger
author_sort Kirchweger, Patrick
collection PubMed
description INTRODUCTION: Pretherapeutic detectable circulating tumor DNA (ctDNA) represents a promising prognostic biomarker for predicting relapse and overall survival in patients with metastatic pancreatic cancer. However, the prognostic value of ctDNA dynamics during treatment has not been studied thus far. We aimed to investigate the correlation between the change of ctDNA levels and response to treatment in patients treated by systemic therapy. MATERIAL AND METHODS: CtDNA detection using liquid biopsy (droplet digital PCR (ddPCR) utilizing KRAS G12/13 and, if negative, Q61 commercial test kits) was prospectively performed on patients with stage IV pancreatic cancer i) prior to initiation of systemic chemotherapy and ii) serially every 2 weeks until restaging. Detection rates, levels of ctDNA, and the course of the relative ctDNA change (ctDNA kinetics) were correlated to treatment response and clinical outcome. RESULTS: The detection rate at baseline was 64.3% (45/70), and complete serial measurement records were available for 32 ctDNA-positive patients. Reduction of ctDNA levels below 57.9% of its baseline value at week 2 after treatment initiation was significantly predictive of response to treatment (area under the curve (AUC) = 0.918, sensitivity 91.67%, and specificity 100%) and was associated with prolonged overall survival (OS) (5.7 vs. 11.4 months, p = 0.006) and progression-free survival (PFS) (2.5 vs. 7.7 months, p < 0.000) regardless of treatment line. Pretherapeutic ctDNA detection was independently associated with worse OS in patients receiving a first-line regimen (7 vs. 11.3 months, p = 0.046) and regardless of treatment line (11.4 vs. 15.9 months, p = 0.045) as well as worse PFS (3.4 vs. 10.8 months, p = 0.018). CONCLUSION: The change in magnitude of ctDNA during systemic treatment allows the prediction of treatment response and is associated with both OS and PFS. This finding adds significant clinical potential to the already established prognostic value of ctDNA positivity in metastatic pancreatic cancer.
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spelling pubmed-94683692022-09-14 Prediction of response to systemic treatment by kinetics of circulating tumor DNA in metastatic pancreatic cancer Kirchweger, Patrick Kupferthaler, Alexander Burghofer, Jonathan Webersinke, Gerald Jukic, Emina Schwendinger, Simon Wundsam, Helwig Biebl, Matthias Petzer, Andreas Rumpold, Holger Front Oncol Oncology INTRODUCTION: Pretherapeutic detectable circulating tumor DNA (ctDNA) represents a promising prognostic biomarker for predicting relapse and overall survival in patients with metastatic pancreatic cancer. However, the prognostic value of ctDNA dynamics during treatment has not been studied thus far. We aimed to investigate the correlation between the change of ctDNA levels and response to treatment in patients treated by systemic therapy. MATERIAL AND METHODS: CtDNA detection using liquid biopsy (droplet digital PCR (ddPCR) utilizing KRAS G12/13 and, if negative, Q61 commercial test kits) was prospectively performed on patients with stage IV pancreatic cancer i) prior to initiation of systemic chemotherapy and ii) serially every 2 weeks until restaging. Detection rates, levels of ctDNA, and the course of the relative ctDNA change (ctDNA kinetics) were correlated to treatment response and clinical outcome. RESULTS: The detection rate at baseline was 64.3% (45/70), and complete serial measurement records were available for 32 ctDNA-positive patients. Reduction of ctDNA levels below 57.9% of its baseline value at week 2 after treatment initiation was significantly predictive of response to treatment (area under the curve (AUC) = 0.918, sensitivity 91.67%, and specificity 100%) and was associated with prolonged overall survival (OS) (5.7 vs. 11.4 months, p = 0.006) and progression-free survival (PFS) (2.5 vs. 7.7 months, p < 0.000) regardless of treatment line. Pretherapeutic ctDNA detection was independently associated with worse OS in patients receiving a first-line regimen (7 vs. 11.3 months, p = 0.046) and regardless of treatment line (11.4 vs. 15.9 months, p = 0.045) as well as worse PFS (3.4 vs. 10.8 months, p = 0.018). CONCLUSION: The change in magnitude of ctDNA during systemic treatment allows the prediction of treatment response and is associated with both OS and PFS. This finding adds significant clinical potential to the already established prognostic value of ctDNA positivity in metastatic pancreatic cancer. Frontiers Media S.A. 2022-08-30 /pmc/articles/PMC9468369/ /pubmed/36110940 http://dx.doi.org/10.3389/fonc.2022.902177 Text en Copyright © 2022 Kirchweger, Kupferthaler, Burghofer, Webersinke, Jukic, Schwendinger, Wundsam, Biebl, Petzer and Rumpold https://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
Kirchweger, Patrick
Kupferthaler, Alexander
Burghofer, Jonathan
Webersinke, Gerald
Jukic, Emina
Schwendinger, Simon
Wundsam, Helwig
Biebl, Matthias
Petzer, Andreas
Rumpold, Holger
Prediction of response to systemic treatment by kinetics of circulating tumor DNA in metastatic pancreatic cancer
title Prediction of response to systemic treatment by kinetics of circulating tumor DNA in metastatic pancreatic cancer
title_full Prediction of response to systemic treatment by kinetics of circulating tumor DNA in metastatic pancreatic cancer
title_fullStr Prediction of response to systemic treatment by kinetics of circulating tumor DNA in metastatic pancreatic cancer
title_full_unstemmed Prediction of response to systemic treatment by kinetics of circulating tumor DNA in metastatic pancreatic cancer
title_short Prediction of response to systemic treatment by kinetics of circulating tumor DNA in metastatic pancreatic cancer
title_sort prediction of response to systemic treatment by kinetics of circulating tumor dna in metastatic pancreatic cancer
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9468369/
https://www.ncbi.nlm.nih.gov/pubmed/36110940
http://dx.doi.org/10.3389/fonc.2022.902177
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