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Circulating KRAS G12D but not G12V is associated with survival in metastatic pancreatic ductal adenocarcinoma.
- Source :
-
Nature communications [Nat Commun] 2024 Jul 09; Vol. 15 (1), pp. 5763. Date of Electronic Publication: 2024 Jul 09. - Publication Year :
- 2024
-
Abstract
- While high circulating tumor DNA (ctDNA) levels are associated with poor survival for multiple cancers, variant-specific differences in the association of ctDNA levels and survival have not been examined. Here we investigate KRAS ctDNA (ctKRAS) variant-specific associations with overall and progression-free survival (OS/PFS) in first-line metastatic pancreatic ductal adenocarcinoma (mPDAC) for patients receiving chemoimmunotherapy ("PRINCE", NCT03214250), and an independent cohort receiving standard of care (SOC) chemotherapy. For PRINCE, higher baseline plasma levels are associated with worse OS for ctKRAS G12D (log-rank p = 0.0010) but not G12V (p = 0.7101), even with adjustment for clinical covariates. Early, on-therapy clearance of G12D (p = 0.0002), but not G12V (p = 0.4058), strongly associates with OS for PRINCE. Similar results are obtained for the SOC cohort, and for PFS in both cohorts. These results suggest ctKRAS G12D but not G12V as a promising prognostic biomarker for mPDAC and that G12D clearance could also serve as an early biomarker of response.<br /> (© 2024. The Author(s).)
- Subjects :
- Humans
Female
Male
Middle Aged
Aged
Prognosis
Antineoplastic Combined Chemotherapy Protocols therapeutic use
Mutation
Progression-Free Survival
Neoplasm Metastasis
Carcinoma, Pancreatic Ductal genetics
Carcinoma, Pancreatic Ductal mortality
Carcinoma, Pancreatic Ductal blood
Carcinoma, Pancreatic Ductal pathology
Carcinoma, Pancreatic Ductal drug therapy
Proto-Oncogene Proteins p21(ras) genetics
Pancreatic Neoplasms genetics
Pancreatic Neoplasms blood
Pancreatic Neoplasms mortality
Pancreatic Neoplasms pathology
Pancreatic Neoplasms drug therapy
Circulating Tumor DNA blood
Circulating Tumor DNA genetics
Biomarkers, Tumor blood
Biomarkers, Tumor genetics
Subjects
Details
- Language :
- English
- ISSN :
- 2041-1723
- Volume :
- 15
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Nature communications
- Publication Type :
- Academic Journal
- Accession number :
- 38982051
- Full Text :
- https://doi.org/10.1038/s41467-024-49915-5