Related Experiment Video
Updated: Jun 21, 2025

06:46
Competing-Risk Nomogram for Predicting Cancer-Specific Survival in Multiple Primary Colorectal Cancer Patients after Surgery
Published on: September 27, 2024
248
Genetic Profiling and Survival Outcomes in Romanian Colorectal Cancer Patients.
Alexandra Vesa1, Octavian Maghiar2, Ovidiu Pop1
1Morphological Sciences, University of Oradea, Faculty of Medicine and Pharmacy, Oradea, ROU.
Cureus
|July 15, 2024
Summary
KRAS and BRAF mutations in colorectal cancer impact survival, with BRAF mutations indicating a worse prognosis. Understanding these mutations is key for personalized treatment strategies.
Area of Science:
- Oncology
- Genetics
- Molecular Biology
Background:
- Colorectal cancer (CRC) is a globally prevalent malignancy, ranking third in incidence and second in mortality.
- KRAS and BRAF mutations are critical biomarkers in CRC, influencing treatment decisions and patient outcomes.
- Personalized medicine approaches increasingly rely on understanding these genetic alterations in CRC.
Purpose of the Study:
- To analyze the impact of KRAS and BRAF mutations on survival and mortality in colorectal cancer patients.
- To compare outcomes between patients with mutant versus wild-type KRAS/BRAF genes.
- To evaluate the prognostic significance of specific mutations (KRAS vs. BRAF) in CRC.
Main Methods:
- Retrospective study of 118 colorectal cancer patients (2018-2022).
- Data collected from Oradea County Emergency Clinical Hospital and Pelican Oradea Hospital.
- Genetic testing for KRAS/BRAF mutations, with patients grouped by mutation status.
Main Results:
- One-year survival: 84.74% (mutant) vs. 67.96% (wild-type).
- Five-year survival showed no significant difference (33.54% mutant vs. 25.93% wild-type).
- BRAF mutation associated with significantly worse prognosis (8.3 months survival) compared to KRAS (38.6 months survival) and higher mortality (100% for BRAF vs. 44.89% for KRAS).
Conclusions:
- No significant difference in overall survival between mutant and wild-type groups, but higher survival observed in the mutant group.
- Wild-type tumors had a higher mortality rate in the first year post-diagnosis.
- BRAF mutations confer a significantly worse prognosis than KRAS mutations in colorectal cancer.

