| Autor: |
Csoma SL; Department of Pathology, Faculty of Medicine, University of Debrecen, H-4032 Debrecen, Hungary., Madarász K; Department of Pathology, Faculty of Medicine, University of Debrecen, H-4032 Debrecen, Hungary., Chang Chien YC; Department of Pathology, Faculty of Medicine, University of Debrecen, H-4032 Debrecen, Hungary., Emri G; Department of Dermatology, Faculty of Medicine, University of Debrecen, H-4032 Debrecen, Hungary., Bedekovics J; Department of Pathology, Faculty of Medicine, University of Debrecen, H-4032 Debrecen, Hungary., Méhes G; Department of Pathology, Faculty of Medicine, University of Debrecen, H-4032 Debrecen, Hungary., Mokánszki A; Department of Pathology, Faculty of Medicine, University of Debrecen, H-4032 Debrecen, Hungary. |
| Abstrakt: |
Here, we investigate the correlation and statistical analyses between histological staging and molecular alterations in tumor-derived (tdDNA) and cell-free DNA (cfDNA) obtained from early-stage primary cutaneous melanoma (PCM) patients using digital PCR (dPCR) for the detection of the BRAF p.V600E somatic pathogenic variant. In the prospective study, a total of 68 plasma and paired tdDNA samples, and in the retrospective cohort, a total of 100 tdDNA samples were analyzed using dPCR and reverse hybridization StripAssay. The Breslow depth (BD) and Clark level were applied to categorize the study population. Our results demonstrate that dPCR is a highly sensitive and specific method for the detection of BRAF p.V600E somatic variants in cfDNA samples from PCM patients. A strong correlation was detected between BD and cfDNA concentration in all mutant and negative cases, between the tdDNA concentration and the tumor-derived variant allele frequency (VAF) of BRAF p.V600E, between the tdVAF and the cfVAF in all cases, and between the cfDNA and cfVAF in mutant cases. The tdVAF and cfVAF of BRAF p.V600E and cfDNA concentration were the highest in Clark's V category. The cfDNA concentration was statistically significantly higher in Clark's III, IV, and V groups compared to cases with a better prognosis. It can also be explained by the fact that cases with a more advanced stage classification release more cfDNA into the peripheral circulation. |
