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DOI: 10.1055/s-0045-1809077
Minimal Invasive Detection of Circulating Biomarkers in Pediatric Cancer Patients Undergoing Chimeric Antigen Receptor
Pediatric tumors pose therapeutic challenges due to genetic heterogeneity and limited precision oncology targets. Chimeric Antigen Receptor T-Cell (CART) therapy has recently emerged as an option when other treatments fail. Traditional tumor monitoring relies on invasive biopsies, limiting therapy response assessment frequency, while liquid biopsies (LB) offer a minimally invasive alternative for dynamic tumor evaluation. This study tracks CART therapy response in pediatric cancer through serial LBs to analyze tumor cell turnover and molecular changes. Cell-free DNA (cfDNA) was isolated from cerebrospinal fluid (CSF) before, during, and after therapy application and analyzed using low-coverage whole-genome sequencing, methylation sequencing, and proteome profiling. Tumor as well as cfDNA-specific alterations, CNV patterns, and dynamic methylation changes enabled time-resolved tumor evolution analysis. Proteome data detected CAR target expression. Long-term minimal residual disease detection after successful therapy demonstrated that LBs complement standard-of-care MRI diagnostics. Their integration into future CART trials is crucial to assess full prognostic value.
Publication History
Article published online:
09 May 2025
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