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July 26, 2026ESMO Gastrointestinal Oncology0 citationsOpen Access

Real-world analysis of ctDNA and other biomarkers in patients with curatively resected stage I-III biliary tract cancer

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MMM. MallaAEAbdullah EsmailATA. Tin

Key Points

  • This study aims to evaluate ctDNA as a prognostic biomarker for detecting molecular residual disease and recurrence in resected biliary tract cancer patients.
  • Retrospective analysis of data from 167 patients with stage I-III resectable biliary tract cancer.
  • Patients underwent ctDNA analysis using a personalized 16-plex multiplex PCR assay.
  • Data collected included plasma samples taken preoperatively and during post-definitive treatment surveillance.
  • ctDNA detection rates were 23% during the molecular residual disease window and 38% during post-definitive treatment surveillance.
  • ctDNA positivity was significantly associated with inferior relapse-free survival (HR 15.86, 95% CI 4.69-53.6, P < 0.001) and overall survival (HR 14.93, 95% CI 5.33-41.9, P < 0.001).
  • Traditional biomarkers carbohydrate antigen 19-9 and carcinoembryonic antigen were not significantly prognostic.

Abstract

Background Growing evidence supports the prognostic and predictive value of circulating tumor DNA (ctDNA) in gastrointestinal cancers. This study evaluated ctDNA as a prognostic biomarker for detecting molecular residual disease (MRD) and recurrence in patients with resected biliary tract cancer (BTC). Materials and methods We retrospectively analyzed real-world data from patients ( N = 167) with stage I-III resectable BTC who underwent ctDNA analysis using a personalized, tumor-informed 16-plex multiplex PCR-coupled next-generation sequencing assay (Signatera TM ; Natera, Inc., Austin, TX) between July 2020 and February 2024. Plasma samples ( n = 751) were collected preoperatively, postsurgically (2-12 weeks; MRD window), and longitudinally (postdefinitive treatment surveillance). ctDNA results were compared with traditional biomarkers carbohydrate antigen 19-9 and carcinoembryonic antigen. Results The median follow-up was 21 months (range 2-97). ctDNA detection rates during MRD and postdefinitive treatment surveillance windows were 23% (19 of 82) and 38% (31 of 82), respectively. ctDNA positivity during MRD and postdefinitive treatment surveillance was significantly associated with inferior relapse-free survival (RFS) and overall survival (OS). ctDNA positivity was the most significant prognostic factor associated with RFS during the MRD window hazard ratio (HR) 15.86, 95% CI 4.69-53.6, P < 0.001 and during postdefinitive treatment surveillance (HR 14.93, 95% CI 5.33-41.9, P < 0.001) by multivariate analysis. In contrast, carbohydrate antigen 19-9 and carcinoembryonic antigen were not significantly prognostic in either setting. Conclusions Patients with ctDNA positivity during the MRD and postdefinitive treatment surveillance windows demonstrated significantly inferior RFS and OS, and ctDNA was more accurate than current clinical biomarkers. These findings highlight the value of ctDNA monitoring in improving prognostication in BTC, with the potential to enhance post-operative risk stratification and inform surveillance strategies through earlier detection of recurrence.

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Cite This Study

Malla et al. (2026) studied this question.

synapsesocial.com/papers/6a65a49fd3aea3239cd77259https://doi.org/10.1016/j.esmogo.2026.100344
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