⚠️ Early Evidence Signal
Pancreatic cancer has high recurrence rates even after surgery and chemotherapy, largely due to undetected minimal residual disease (MRD). Standard next-generation sequencing (NGS)–based liquid biopsy approaches often lack sensitivity in low-shedding tumors.
Clinical Considerations
- ddPCR detected tumor DNA in 65% of patients vs 17% with NGS at diagnosis
- Detection persisted post-treatment (~60% after chemotherapy, ~56% after surgery)
- Identified a previously unrecognized high-risk cohort:
- NGS-negative but ddPCR-positive
- Median survival 27 months vs 41 months in double-negative patients
- Enables mutation-aligned monitoring, particularly relevant for emerging KRAS-targeted therapies
- Findings are based on single-center data (n=106) and require validation
Practice Applications
- Expect under-detection with standard NGS assays in pancreatic cancer
- Mutation-specific ctDNA assays may improve MRD detection
- Potential future integration:
- Serial ctDNA monitoring
- Earlier intervention at molecular recurrence
- Clinical adoption remains premature pending validation
PATIENT EDUCATION
OBESITY/WEIGHT MANAGEMENT
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