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Updated: Jun 24, 2026
Detection and Monitoring of Tumor Associated Circulating DNA in Patient Biofluids
Published on: June 8, 2019
Perioperative ctDNA as a prognostic biomarker in endometrial cancer - the CODEC study
Rachel L Delahunty1, Madawa Jayawardana2, Rainier Arnolda3
1Epworth HealthCare, Melbourne, Victoria, Australia; Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia; The Royal Women's Hospital, Melbourne, Victoria, Australia; Sir Peter MacCallum Department of Oncology, The University of Melbourne, Victoria, Australia; Deakin University, Geelong, Victoria, Australia.
Purpose:
Biomarkers to predict relapse and guide adjuvant therapy selection are needed in endometrial cancer (EC), one of the few cancers increasing in incidence and mortality. Assessment of circulating tumour DNA (ctDNA) at multiple perioperative time points has not been explored in EC. This study aimed to evaluate the prognostic utility of ctDNA across four perioperative time points, explore ctDNA dynamics, and compare ctDNA-derived tumour burden with 18F-fluorodeoxyglucose (FDG)-PET/CT and MRI.
Patients And Methods:
Participants with Type 2 EC planned for surgery and consenting to the collection of biospecimens were enrolled prior to surgery and followed prospectively. Participants had preoperative imaging, and tumour sequencing was performed using hybrid capture, which guided the design of droplet digital PCR (ddPCR) assays for ctDNA analysis. The primary study endpoint was relapse free survival.
Results:
Fifty participants were enrolled in the CODEC study. Genomic findings were consistent with the established molecular landscape of EC. Detection of ctDNA postoperatively at 24 h (Time Point 2B) and at 2-6 weeks (Time Point 3) was associated with poorer relapse-free survival. No significant association with outcome was observed for preoperative (Time Point 1) or intraoperative (Time Point 2A) ctDNA. Preoperative ctDNA correlated with FDG-PET- and MRI-defined tumour volume.
Conclusion:
These findings are hypothesis-generating and support the prognostic relevance of postoperative ctDNA assessment in EC with the 2-6 week postoperative window the most clinically informative time point for detecting minimal residual disease. Further studies are required to validate these findings and determine whether ctDNA can guide adjuvant therapy selection.