Cell-Free Methylated PTGER4 and SHOX2 Plasma DNA as a Biomarker for Therapy Monitoring and Prognosis in Advanced Stage NSCLC Patients

Author:

Fleischhacker Michael1,Arslan Erkan2,Reinicke Dana3,Eisenmann Stefan3,Theil Gerit3,Kollmeier Jens4ORCID,Schäper Christoph5,Grah Christian6,Klawonn Frank78,Holdenrieder Stefan9,Schmidt Bernd1

Affiliation:

1. Klinik für Innere Medizin—Schwerpunkt Pneumologie und Schlafmedizin, DRK Kliniken Berlin/Mitte, 13359 Berlin, Germany

2. Lungenarztpraxis Berlin-Reinickendorf, 13403 Berlin, Germany

3. Department für Innere Medizin, Universitätsklinikum Halle/Saale, 06120 Halle (Saale), Germany

4. Lungenklinik Heckeshorn, Helios Klinikum Emil von Behring, 14165 Berlin, Germany

5. Klinik und Poliklinik für Innere Medizin B, Universitätsmedizin Greifswald, 17475 Greifswald, Germany

6. Gemeinschaftskrankenhaus Havelhöhe, Pneumologie und Lungenkrebszentrum, 14089 Berlin, Germany

7. Department of Computer Science, Ostfalia University, 38302 Wolfenbüttel, Germany

8. Biostatistics, Helmholtz Centre for Infection Research, 38124 Braunschweig, Germany

9. Munich Biomarker Research Center, Institute of Laboratory Medicine, German Heart Centre, Technical University Munich, Lazarettstraße 36, 80636 Munich, Germany

Abstract

Notwithstanding some improvement in the earlier detection of patients with lung cancer, most of them still present with a late-stage disease at the time of diagnosis. Next to the most frequently utilized factors affecting the prognosis of lung cancer patients (stage, performance, and age), the recent application of biomarkers obtained by liquid profiling has gained more acceptance. In our study, we aimed to answer these questions: (i) Is the quantification of free-circulating methylated PTGER4 and SHOX2 plasma DNA a useful method for therapy monitoring, and is this also possible for patients treated with different therapy regimens? (ii) Is this approach possible when blood-drawing tubes, which allow for a delayed processing of blood samples, are utilized? Baseline values for mPTGER4 and mSHOX2 do not allow for clear discrimination between different response groups. In contrast, the combination of the methylation values for both genes shows a clear difference between responders vs. non-responders at the time of re-staging. Furthermore, blood drawing into tubes stabilizing the sample allows researchers more flexibility.

Publisher

MDPI AG

Subject

Clinical Biochemistry

Reference28 articles.

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