Ultrasensitive ctDNA monitoring for organ preservation in patients with locally advanced rectal cancer

Optimal selection of patients with locally advanced rectal cancer for watch and wait (WW) and optimal management during follow-up remain challenging. We employed a primary-tumor-informed whole genome sequencing (WGS) assay to detect circulating tumor DNA (ctDNA) and estimate tumor fraction (TF) before, during and after neoadjuvant therapy. ctDNA was detected in 95% of baseline samples, and TF was a significant baseline predictor of sustained clinical complete response (scCR). High TF during or after neoadjuvant therapy was associated with lower likelihood of scCR and higher risk of relapse. Very low TF during surveillance was detected in a large proportion of patients who did not experience a recurrence, suggesting the existence of persisting low amounts of ctDNA. WGS-based ctDNA assessment thus provides high sensitivity, which is crucial for treatment de-escalation, but additional research is needed to also ensure good specificity (the trial is registered in ClinicalTrials.gov with the identifier NCT02008656).

Authors

Institutions

Publication Details

Journal
npj Precision Oncology
Published
2025-12-11
DOI
https://doi.org/10.1038/s41698-025-01208-w
Citations
1
Primary Topic
Cancer Genomics and Diagnostics
Type
article
Field-Weighted Citation Impact
0.94
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Ultrasensitive ctDNA monitoring for organ preservation in patients with locally advanced rectal cancer

Julio García‐Aguilar, Christina Y. Lee, Chin‐Tung Chen, Iman Tavassoly et al.
1 citations
npj Precision Oncology
Cancer Genomics and Diagnostics
0.94
article

Ultrasensitive ctDNA monitoring for organ preservation in patients with locally advanced rectal cancer

Julio García‐Aguilar, Christina Y. Lee, Chin‐Tung Chen, Iman Tavassoly, Walid K. Chatila, Francisco Sánchez-Vega, Madison Darmofal, Adam J. Widman, Michael F. Berger, Rona Yaeger, Brian Houck‐Loomis, Paolo Manca, Samuel Terkper Ahuno, Dana M. Omer, Santiago González, Asaf Zviran, Dylan Domenico, Elli Papaemmanuil, Ino de Bruijn, Farheen Shah
article en
1 citations

Abstract

Optimal selection of patients with locally advanced rectal cancer for watch and wait (WW) and optimal management during follow-up remain challenging. We employed a primary-tumor-informed whole genome sequencing (WGS) assay to detect circulating tumor DNA (ctDNA) and estimate tumor fraction (TF) before, during and after neoadjuvant therapy. ctDNA was detected in 95% of baseline samples, and TF was a significant baseline predictor of sustained clinical complete response (scCR). High TF during or after neoadjuvant therapy was associated with lower likelihood of scCR and higher risk of relapse. Very low TF during surveillance was detected in a large proportion of patients who did not experience a recurrence, suggesting the existence of persisting low amounts of ctDNA. WGS-based ctDNA assessment thus provides high sensitivity, which is crucial for treatment de-escalation, but additional research is needed to also ensure good specificity (the trial is registered in ClinicalTrials.gov with the identifier NCT02008656).

npj Precision OncologyVol. 10(1)
Memorial Sloan Kettering Cancer Center (US), ID Genomics (United States) (US), Fondazione IRCCS Istituto Nazionale dei Tumori (IT)
Openalex Percentile: Top 18%
Cancer Genomics and Diagnostics
0.94
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.