Přehled o publikaci
2026
Detection of KRAS, NRAS and BRAF mutations in liquid biopsy from patients with colorectal cancer
ONDRÁŠKOVÁ, Kateřina; Matouš CWIK; Ondřej HORKÝ; Jitka BERKOVCOVÁ; Jitka HOLČÁKOVÁ et al.Basic information
Original name
Detection of KRAS, NRAS and BRAF mutations in liquid biopsy from patients with colorectal cancer
Authors
ONDRÁŠKOVÁ, Kateřina; Matouš CWIK; Ondřej HORKÝ; Jitka BERKOVCOVÁ; Jitka HOLČÁKOVÁ; Martin BARTOŠÍK; Tomáš KAZDA; Klára MRÁZOVÁ; Michal UHER; Igor KISS and Roman HRSTKA
Edition
ONCOLOGY RESEARCH, COGNIZANT COMMUNICATION CORP, 2026, 0965-0407
Other information
Language
English
Type of outcome
Article in a journal
Country of publisher
United States of America
Confidentiality degree
is not subject to a state or trade secret
References:
Marked to be transferred to RIV
No
Organization
Přírodovědecká fakulta – Repository – Repository
UT WoS
EID Scopus
Keywords (in Czech)
tekutá biopsie; kolorektální karcinom; kapénková digitální PCR (ddPCR); mutace protoonkogenu Kirstenova virového sarkomu potkana (KRAS)
Keywords in English
Liquid biopsy; colorectal cancer (CRC); droplet digital PCR (ddPCR); Kirsten Rat Sarcoma Viral Proto- Oncogene (KRAS) mutation
Links
BBMRI.cz IV, large research infrastructures.
Changed: 6/3/2026 00:51, RNDr. Daniel Jakubík
Abstract
In the original language
Objectives: Cancer treatment relies heavily on accurate diagnosis and effective monitoring of the disease. These processes often involve invasive procedures, such as colonoscopy, to detect malignant tissues, followed by molecular analyses to determine relevant biomarkers. This study aimed to evaluate the clinical performance of droplet digital PCR (ddPCR) for detecting Kirsten Rat Sarcoma Viral Proto-Oncogene (KRAS), Neuroblastoma RAS Viral Oncogene Homolog (NRAS), and B-Raf Murine Sarcoma Viral Oncogene Homolog B (BRAF) mutations in circulating tumor DNA (ctDNA) from colorectal cancer patients using liquid biopsy. Methods: ctDNA was isolated from colorectal cancer (CRC) patients (n = 110) and analyzed for KRAS, BRAF, and NRAS mutations. The ctDNA obtained through liquid biopsy was analyzed using ddPCR, and the findings were compared with sequencing data from tumor DNA archived in formalin-fixed paraffin-embedded (FFPE) blocks. Results: For KRAS mutations, ddPCR achieved a sensitivity of 72.0% and a specificity of 71.4%. However, when pooling all target mutations (KRAS, NRAS and BRAF), the overall sensitivity and specificity were lower, at 48.3% and 51.1%, respectively. Conclusion: The results of this study indicate that the ddPCR analysis of ctDNA may provide complementary information for the molecular diagnosis of CRC patients.