Department für Innere Medizin, Universitätsklinikum Halle/Saale, 06120 Halle (Saale), Germany
Stefan Eisenmann
Department für Innere Medizin, Universitätsklinikum Halle/Saale, 06120 Halle (Saale), Germany
Gerit Theil
Department für Innere Medizin, Universitätsklinikum Halle/Saale, 06120 Halle (Saale), Germany
Jens Kollmeier
Lungenklinik Heckeshorn, Helios Klinikum Emil von Behring, 14165 Berlin, Germany
Christoph Schäper
Klinik und Poliklinik für Innere Medizin B, Universitätsmedizin Greifswald, 17475 Greifswald, Germany
Christian Grah
Gemeinschaftskrankenhaus Havelhöhe, Pneumologie und Lungenkrebszentrum, 14089 Berlin, Germany
Frank Klawonn
Department of Computer Science, Ostfalia University, 38302 Wolfenbüttel, Germany
Stefan Holdenrieder
Munich Biomarker Research Center, Institute of Laboratory Medicine, German Heart Centre, Technical University Munich, Lazarettstraße 36, 80636 Munich, Germany
Bernd Schmidt
Klinik für Innere Medizin—Schwerpunkt Pneumologie und Schlafmedizin, DRK Kliniken Berlin/Mitte, 13359 Berlin, Germany
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.