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Associations with other cancer-related biomarkers might contribute to poor outcomes in RAS-altered, younger patients with colorectal cancer.
- Source :
-
The oncologist [Oncologist] 2024 Sep 06; Vol. 29 (9), pp. e1228-e1230. - Publication Year :
- 2024
-
Abstract
- Colorectal cancer (CRC) is a common cancer in younger adults. In patients undergoing liver resection with RAS-altered CRCs, there is evidence suggesting younger patients have worse outcomes than older patients. To explain this pattern, differences in associations between RAS status and other cancer-related biomarkers in tumors from younger versus older patients with CRC were evaluated in a cohort of 925 patients with CRC, 277 (30.0%) of whom were ≤50 years old, and 454 (49.1%) who had RAS-altered tumors. For 3 biomarkers, RNF43, APC, and microsatellite instability (MSI), the association with RAS status was significantly modified by age after adjustment for multiple testing. Specifically, younger patients with RAS-altered tumors were more likely to be MSI-high, RNF43 mutated, and APC wild type. These differences might contribute to the observed pattern of diminished survival in younger versus older patients with CRC with RAS-mutated tumors undergoing liver metastasis resection.<br /> (© The Author(s) 2024. Published by Oxford University Press.)
- Subjects :
- Humans
Male
Middle Aged
Female
Adult
Aged
Mutation
Age Factors
Liver Neoplasms genetics
Liver Neoplasms pathology
Ubiquitin-Protein Ligases genetics
Ubiquitin-Protein Ligases metabolism
ras Proteins genetics
ras Proteins metabolism
Prognosis
Adenomatous Polyposis Coli Protein genetics
Colorectal Neoplasms genetics
Colorectal Neoplasms pathology
Colorectal Neoplasms surgery
Colorectal Neoplasms mortality
Biomarkers, Tumor genetics
Biomarkers, Tumor metabolism
Microsatellite Instability
Subjects
Details
- Language :
- English
- ISSN :
- 1549-490X
- Volume :
- 29
- Issue :
- 9
- Database :
- MEDLINE
- Journal :
- The oncologist
- Publication Type :
- Academic Journal
- Accession number :
- 38886182
- Full Text :
- https://doi.org/10.1093/oncolo/oyae153