Evidence map›Paper›PMID 41483629›Full record

ArticleESMO open2026

Added value of tumor-stroma ratio to postsurgery circulating tumor DNA and pTN stage in risk stratification of patients with stage III colon cancer treated with adjuvant chemotherapy.

I A Franken, F Heilijgers, M-C E Bakker, C Rubio-Alarcón, F H van der Baan, M Lemmens, P Delis-van Diemen, M Sausen, G A Meijer, M Koopman and 4 more

Abstract read
In one paragraph

Article in ESMO open, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors.

I A FrankenUniversity Medical Center Utrecht, Department of Medical Oncology, Utrecht University, Utrecht, The Netherlands.
F HeilijgersLeiden University Medical Center, Department of Surgery, Leiden, The Netherlands.
M-C E BakkerUniversity Medical Center Utrecht, Department of Medical Oncology, Utrecht University, Utrecht, The Netherlands.
C Rubio-AlarcónThe Netherlands Cancer Institute, Department of Pathology, Amsterdam, The Netherlands.
F H van der BaanUniversity Medical Center Utrecht, Department of Medical Oncology, Utrecht University, Utrecht, The Netherlands.
M LemmensThe Netherlands Cancer Institute, Department of Pathology, Amsterdam, The Netherlands.
P Delis-van DiemenThe Netherlands Cancer Institute, Department of Pathology, Amsterdam, The Netherlands.
M SausenLabcorp, Baltimore, USA.
G A MeijerThe Netherlands Cancer Institute, Department of Pathology, Amsterdam, The Netherlands.
M KoopmanUniversity Medical Center Utrecht, Department of Medical Oncology, Utrecht University, Utrecht, The Netherlands.
G R VinkUniversity Medical Center Utrecht, Department of Medical Oncology, Utrecht University, Utrecht, The Netherlands; Department of Research and Development, Netherlands Comprehensive Cancer Organisation, Utrecht, The Netherlands.
R J A FijnemanThe Netherlands Cancer Institute, Department of Pathology, Amsterdam, The Netherlands.
W E MeskerLeiden University Medical Center, Department of Surgery, Leiden, The Netherlands.
J M L RoodhartUniversity Medical Center Utrecht, Department of Medical Oncology, Utrecht University, Utrecht, The Netherlands. Electronic address: j.roodhart@umcutrecht.nl.

Funding

ECOG-ACRIN Thoracic Malignancies Integrated Translational Science CenterUG1CA233259 · NCI · EMORY UNIVERSITY · PI CARBONE, DAVID P., LEAL, TICIANA · 2019 to 2025
$5.1M
Large-Scale Genetic Analyses of Human CancerR01CA121113 · NCI · JOHNS HOPKINS UNIVERSITY · PI ANAGNOSTOU, VALSAMO, VELCULESCU, VICTOR E. · 2006 to 2022
$4.3M
NCI NIH HHS R01 CA121113NCI NIH HHS UG1 CA233259
6 · The paper itself

Abstract

backgroundPatients with stage III colon cancer (CC) are routinely treated with resection followed by adjuvant chemotherapy (ACT). Half of patients are cured by surgery alone and overtreated with ACT, yet another ∼30% experience disease recurrence. Upfront risk stratification requires biomarkers beyond the conventional pathological stage (pTN). Detection of postsurgery circulating tumor DNA (ctDNA) is indicative of minimal residual disease and prognostic of recurrence. However, its negative predictive value is insufficient to guide treatment de-escalation. This study aimed to investigate whether adding tumor-stroma ratio (TSR) can improve patient risk stratification. PATIENTS AND

methodsThis study included 206 patients from PLCRC-PROVENC3 based on radical resection of stage III CC followed by ACT. Postsurgery ctDNA status was determined using Labcorp® Plasma Detect™. On a hematoxylin-eosin resection section, the TSR was scored by trained observers and dichotomized as stroma-low (≤50% stroma) versus stroma-high (>50%). The primary outcome was time to recurrence in univariable and multivariable Cox analyses to inform risk-group stratification, reporting hazard ratios (HR) and recurrence risks (RR).

resultsPostsurgery ctDNA was the strongest predictor [n = 26, 3-year RR 65.4% (95% CI 41.3% to 79.6%) versus 16.8% (95% CI 11.0% to 22.3%); HR 6.1 (95% CI 3.4-10.8)], followed by pT4/pN2 [n = 80, HR 3.0 (95% CI 1.7-5.2)] and a stroma-high tumor [n = 88, HR 3.0 (95% CI 1.7-5.2)]. Within the ctDNA-negative subgroup (n = 180), we identified a low-risk group [pT1-3N1 and stroma-low; n = 72, 3-year RR 2.9% (95% CI 0% to 6.7%)], intermediate-risk group [either pT4/N2 or stroma-high; n = 68, 3-year RR 17.2% (95% CI 7.4% to 26.0%), HR 8.2 (95% CI 1.9-36.2)], and high-risk group [pT4/N2 and stroma-high; n = 40, 3-year RR 40.3% (95% CI 22.9% to 53.9%), HR 21.5 (95% CI 5.0-92.3)].

conclusionsAdding TSR to ctDNA and pTN stage improved risk stratification of stage III CC patients receiving ACT. One-third of the patients had none of the biomarkers and could be considered for de-escalation based on their very low RR. In addition to ctDNA-positive patients, ctDNA-negative patients with a pT4/N2 stroma-high tumor may require treatment escalation to reduce their high RR.

Indexed as

Circulating Tumor DNAColonic NeoplasmsAdultAgedBiomarkers, TumorChemotherapy, AdjuvantFemaleHumansMaleMiddle AgedNeoplasm Recurrence, LocalNeoplasm StagingPrognosisRisk AssessmentBiomarkers, TumorCirculating Tumor DNAadjuvant chemotherapybiomarkercirculating tumor DNAcolon cancertumor–stroma ratio

Identifiers

PMID41483629
PMCPMC12805340

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.