Scientific Reports (Jan 2024)

Towards effectiveness of cell free DNA based liquid biopsy in head and neck squamous cell carcinoma

  • Ewelina Kowal-Wisniewska,
  • Katarzyna Jaskiewicz,
  • Anna Bartochowska,
  • Katarzyna Kiwerska,
  • Adam Ustaszewski,
  • Tomasz Gorecki,
  • Maciej Giefing,
  • Jaroslaw Paluszczak,
  • Malgorzata Wierzbicka,
  • Malgorzata Jarmuz-Szymczak

DOI
https://doi.org/10.1038/s41598-024-52031-5
Journal volume & issue
Vol. 14, no. 1
pp. 1 – 11

Abstract

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Abstract Liquid biopsy is a minimally invasive procedure, that uses body fluids sampling to detect and characterize cancer fingerprints. It is of great potential in oncology, however there are challenges associated with the proper handling of liquid biopsy samples that need to be addressed to implement such analysis in patients’ care. Therefore, in this study we performed optimization of pre-analytical conditions and detailed characterization of cfDNA fraction (concentration, length, integrity score) in surgically treated HNSCC patients (n = 152) and healthy volunteers (n = 56). We observed significantly higher cfDNA concentration in patients compared to healthy controls (p < 0.0001) and a time dependent decrease of cfDNA concentration after tumor resection. Our results also revealed a significant increase of cfDNA concentration with age in both, healthy volunteers (p = 0.04) and HNSCC patients (p = 0.000002). Moreover, considering the multitude of HNSCC locations, we showed the lack of difference in cfDNA concentration depending on the anatomical location. Furthermore, we demonstrated a trend toward higher cfDNA length (range 35–10380 and 500–10380 bp) in the group of patients with recurrence during follow-up. In conclusion, our study provide a broad characterization of cfDNA fractions in HNSCC patients and healthy controls. These findings point to several aspects necessary to consider when implementing liquid biopsy in clinical practice including: (I) time required for epithelial regeneration to avoid falsely elevated levels of cfDNA not resulting from active cancer, (II) age-related accumulation of nucleic acids accompanied by less efficient elimination of cfDNA and (III) higher cfDNA length in patients with recurrence during follow-up, reflecting predominance of tumor necrosis.