Cell-Free Methylated PTGER4 and SHOX2 Plasma DNA as a Biomarker for Therapy Monitoring and Prognosis in Advanced Stage NSCLC Patients.
Michael FleischhackerErkan ArslanDana ReinickeStefan EisenmannGerit TheilJens KollmeierChristoph SchäperChristian GrahFrank KlawonnStefan HoldenriederBernd SchmidtPublished in: Diagnostics (Basel, Switzerland) (2023)
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.
Keyphrases
- cell free
- circulating tumor
- small cell lung cancer
- end stage renal disease
- genome wide
- single molecule
- magnetic resonance
- newly diagnosed
- chronic kidney disease
- lymph node
- stem cells
- dna methylation
- computed tomography
- gene expression
- magnetic resonance imaging
- ionic liquid
- smoking cessation
- replacement therapy
- sensitive detection