Evaluation of a novel ctDNA panel shows high sensitivity for detecting endometrial cancer recurrence, indicating its potential clinical utility.
Circulating tumour DNA (ctDNA) has high sensitivity to detect endometrial cancer (EC) recurrence. An EC-specific ctDNA panel (ECctDNA-panel) was designed using TCGA/CPTAC mutation profile datasets and whole exome sequencing data from primary ECs. The ECctDNA-panel was tested using commercial standards to determine the detection limit for known driver variants, before investigating the plasma cell free DNA (cfDNA) from patients with/without recurrence. The ECctDNA-panel was able to detect EC hotspot mutations at >1% AF in 100% (42/42) of primary tumours tested. The ctDNA standards confirmed detection as low as 0.74% VAF in 5 ng template DNA. The ECctDNA-panel detected hotspot variants in 10/14 patients with recurrence and in 1/25 without recurrence: sensitivity/specificity 71.4%/96% and accuracy 87.2%. Potentially actionable mutations were identified in 8/10 ctDNA positive recurrences. We report the development of an ECctDNA-panel that has a high diagnostic accuracy to detect EC recurrence and could be utilised to guide patient’s further management.
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Wadsley et al. (2026) studied this question.
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