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Prediction of Microsatellite Instability in Colorectal Cancer Using Two Internally Validated Radiomic Models.

Antonio Galluzzo1, Ginevra Danti1, Linda Calistri1

  • 1Department of Radiology, Careggi University Hospital, Largo Brambilla 3, 50134 Florence, Italy.

Tomography (Ann Arbor, Mich.)
|November 26, 2025
PubMed
Summary
This summary is machine-generated.

Two radiomic models predict microsatellite instability (MSI) in colorectal cancer (CRC) using preoperative CT scans. These models show promise for non-invasive MSI status prediction, potentially guiding treatment decisions.

Keywords:
IBSIclinical featurescolorectal neoplasmsmetricsmicrosatellite instabilityoverfittingprecision medicineradiomic featuresradiomics

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Area of Science:

  • Radiology
  • Oncology
  • Medical Imaging

Background:

  • Microsatellite instability (MSI) is a key biomarker in colorectal cancer (CRC).
  • Accurate preoperative prediction of MSI status is crucial for treatment selection.
  • Current methods often rely on invasive testing.

Purpose of the Study:

  • To develop and validate radiomic models using preoperative contrast-enhanced computed tomography (PP CT) to predict MSI in CRC patients.
  • To compare the performance of models developed using multi-scanner versus single-scanner data.

Main Methods:

  • 115 CRC patients' PP CT scans were analyzed.
  • Two radiomic models were developed: Model I (multi-scanner) and Model II (single-scanner).
  • Radiomic features (RFs) and clinical data were extracted and analyzed using LASSO regression for feature selection.

Main Results:

  • Model I (2 RFs + 1 clinical feature) achieved AUCs of 0.76 (training) and 0.74 (validation).
  • Model II (3 RFs) achieved AUCs of 0.85 (training) and 0.72 (validation).
  • Both models demonstrated good performance in distinguishing MSI from non-MSI tumors.

Conclusions:

  • Radiomic models show potential as non-invasive preoperative tools for predicting MSI status in CRC.
  • Model I, incorporating clinical features, showed better generalizability and less overfitting compared to Model II.
  • Further validation on larger, diverse datasets is recommended to enhance model generalizability.