HIBRID: histology-based risk-stratification with deep learning and ctDNA in colorectal cancer

Nat Commun. 2025 Aug 14;16(1):7561. doi: 10.1038/s41467-025-62910-8.

Abstract

Although surgical resection is the standard therapy for stage II/III colorectal cancer, recurrence rates exceed 30%. Circulating tumor DNA (ctNDA) detects molecular residual disease (MRD), but lacks spatial and tumor microenvironment information. Here, we develop a deep learning (DL) model to predict disease-free survival from hematoxylin & eosin stained whole slide images in stage II-IV colorectal cancer. The model is trained on the DACHS cohort (n = 1766) and validated on the GALAXY cohort (n = 1404). In GALAXY, the DL model categorizes 304 patients as DL high-risk and 1100 as low-risk (HR 2.31; p < 0.005). Combining DL scores with MRD status improves prognostic stratification in both MRD-positive (HR 1.58; p < 0.005) and MRD-negative groups (HR 2.1; p < 0.005). Notably, MRD-negative patients predicted as DL high-risk benefit from adjuvant chemotherapy (HR 0.49; p = 0.01) vs. DL low-risk (HR = 0.92; p = 0.64). Combining ctDNA with DL-based histology analysis significantly improves risk stratification, with the potential to improve follow-up and personalized adjuvant therapy decisions.

MeSH terms

  • Adult
  • Aged
  • Biomarkers, Tumor / blood
  • Biomarkers, Tumor / genetics
  • Chemotherapy, Adjuvant
  • Circulating Tumor DNA* / blood
  • Circulating Tumor DNA* / genetics
  • Colorectal Neoplasms* / blood
  • Colorectal Neoplasms* / diagnosis
  • Colorectal Neoplasms* / genetics
  • Colorectal Neoplasms* / mortality
  • Colorectal Neoplasms* / pathology
  • Deep Learning*
  • Disease-Free Survival
  • Female
  • Humans
  • Male
  • Middle Aged
  • Neoplasm Recurrence, Local / genetics
  • Neoplasm Staging
  • Neoplasm, Residual / genetics
  • Prognosis
  • Risk Assessment / methods
  • Tumor Microenvironment

Substances

  • Circulating Tumor DNA
  • Biomarkers, Tumor