Design and evaluation of a custom circulating tumour DNA assay to detect endometrial cancer recurrence

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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Publication Details

Journal
npj Precision Oncology
Published
2026-03-23
DOI
https://doi.org/10.1038/s41698-025-01246-4
Primary Topic
Cancer Genomics and Diagnostics
Type
article
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article

Design and evaluation of a custom circulating tumour DNA assay to detect endometrial cancer recurrence

Gemma Donaldson, Moss El, Caroline Cowley, DS Guttery et al.
npj Precision Oncology
Cancer Genomics and Diagnostics
article

Design and evaluation of a custom circulating tumour DNA assay to detect endometrial cancer recurrence

Gemma Donaldson, Moss El, Caroline Cowley, DS Guttery, Catherine Moreman, Anna Collins, Lin Zhang, Roger Hew, Elizabeth Stannard, J. Shaw, M. Wadsley
article en

Abstract

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.

npj Precision OncologyVol. 10(1)
University of Leicester (GB), University Hospitals of Leicester NHS Trust (GB), NIHR Leicester Biomedical Research Centre (GB)
Openalex Percentile: Top 13%
Cancer Genomics and Diagnostics
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Design and evaluation of a custom circulating tumour DNA assay to detect endometrial cancer recurrence — Gemma Donaldson, Moss El, et al. · npj Precision Oncology (2026) | TGRS Research Map | TGRS