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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.
Afiliación
  • Kirchweger P; Gastrointestinal Cancer Center, Ordensklinikum Linz, Linz, Austria.
  • Kupferthaler A; Department of Surgery, Ordensklinikum Linz, Linz, Austria.
  • Burghofer J; Medical Faculty, Johannes Kepler University Linz, Linz, Austria.
  • Webersinke G; Department of Diagnostic and Interventional Radiology, Ordensklinikum Linz, Linz, Austria.
  • Jukic E; Laboratory for Molecular Genetic Diagnostics, Ordensklinikum Linz, Linz, Austria.
  • Schwendinger S; Laboratory for Molecular Genetic Diagnostics, Ordensklinikum Linz, Linz, Austria.
  • Wundsam H; Institute of Human Genetics, Medical University of Innsbruck, Innsbruck, Austria.
  • Biebl M; Institute of Human Genetics, Medical University of Innsbruck, Innsbruck, Austria.
  • Petzer A; Department of Surgery, Ordensklinikum Linz, Linz, Austria.
  • Rumpold H; Department of Surgery, Ordensklinikum Linz, Linz, Austria.
Front Oncol ; 12: 902177, 2022.
Article en En | MEDLINE | ID: mdl-36110940
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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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies / Risk_factors_studies Idioma: En Revista: Front Oncol Año: 2022 Tipo del documento: Article País de afiliación: Austria

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies / Risk_factors_studies Idioma: En Revista: Front Oncol Año: 2022 Tipo del documento: Article País de afiliación: Austria
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