Evidence map›Paper›PMID 39487920›Full record

Observational studyAbdominal radiology (New York)2025

Role of tumor-specific and whole-body imaging biomarkers for prediction of recurrence in patients with stage III colorectal cancer.

Amir A Borhani, Peng Zhang, Brenda Diergaarde, Sophie Darwiche, Kalina Chuperlovska, Stewart C Wang, Robert E Schoen, Grace L Su

Registry-linked trialAbstract readObservational Study
PubMed Publisher
In one paragraph

Observational study in Abdominal radiology (New York), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02842203 (Use of ctDNA for Monitoring of Stage III Colorectal Cancer), which is not on this map. Cited by 1 paper.

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

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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.

NCT02842203 active not recruitingnot on this map

Use of ctDNA for Monitoring of Stage III Colorectal Cancer

TypeobservationalSponsorUniversity of PittsburghRan2016 to 2026Enrolled137ConditionsStage III Colorectal Cancer
3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
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

8 authors.

Amir A BorhaniNorthwestern University, Evanston, USA. amir.borhani@northwestern.edu.
Peng ZhangUniversity of Michigan-Ann Arbor, Ann Arbor, USA.
Brenda DiergaardeUniversity of Pittsburgh, Pittsburgh, USA.
Sophie DarwicheUniversity of Pittsburgh, Pittsburgh, USA.
Kalina ChuperlovskaUniversity Hospital Saint Ivan Rilski, Sofia, Bulgaria.
Stewart C WangUniversity of Michigan-Ann Arbor, Ann Arbor, USA.
Robert E SchoenUniversity of Pittsburgh, Pittsburgh, USA.
Grace L SuUniversity of Michigan-Ann Arbor, Ann Arbor, USA.

Funding

Refinement and Discovery of Nuclear Matrix Protein Markers for Colorectal CancerU01CA152753 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI KINZLER, KENNETH W., SCHOEN, ROBERT E. · 2010 to 2021
$6.8M
NCI NIH HHS U01 CA152753
6 · The paper itself

Abstract

backgroundImaging biomarkers are emerging as non-invasive predictors of cancer prognosis and clinical outcome. We assessed tumor-specific ("radiomics") and body composition imaging features ("morphomics") extracted from baseline pre-treatment CT for prediction of recurrence in patients with stage III colorectal cancer (CRC).

methodsPatients with newly diagnosed stage III CRC were enrolled in this prospective observational study. Patients with available preoperative scans were included (N = 101). The tumor, if visible, was manually segmented and first-order radiomics features were extracted with a commercially available software. The morphomics features (reflecting muscle, fat, and bone characteristics) were extracted in a standardized fashion using a proprietary software and the values were adjusted and normalized based on a reference standard. Time to recurrence was the final outcome. Correlation between demographics, clinical features, radiomics, and morphomics features and outcome were assessed using univariate and multivariate tests as well as Kaplan-Meier and log-rank tests.

resultsMorphomic analysis was performed in all 101 patients. 60 patients had discrete tumors suitable for radiomics analysis. These patients had lower ECOG score (p < 0.05), more muscle mass (p > 0.05), and lower fat density (p > 0.05) compared to the patients in whom radiomics analysis could not be performed. Pathological stage (HR: 2.69; p = 0.03), CEA level after surgery (HR: 1.11 for 1 ng/mL; p < 0.005), bone mineral density (HR: 1.01 for 1 Hounsfield Unit; p < 0.01), and tumor skewness (HR: 0.33 for 1 unit; p < 0.05) had association with recurrence based on both univariate and multivariate analyses. A model using Cox's regression analyses was able to divide the patients into low-, medium-, and high-risk for recurrence.

conclusionsBoth radiomics and morphomics features were independently associated with the risk of CRC recurrence and, when combined, each contributed valuable information to explain risk of recurrence.

trial registrationClinical trial.gov NCT02842203. Patient recruitment occurred between 22/07/2016 and 18/03/2020.

Indexed as

Colorectal NeoplasmsNeoplasm Recurrence, LocalTomography, X-Ray ComputedWhole Body ImagingAdultAgedAged, 80 and overBiomarkers, TumorBody CompositionFemaleHumansMaleMiddle AgedNeoplasm StagingPredictive Value of TestsPrognosisBiomarkers, TumorColorectal cancerImaging biomarkerMorphomicsRadiomicsTumor recurrence

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Registered trials

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.