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A consensus molecular subtypes classification strategy for clinical colorectal cancer tissues

  • Tim R. de Back
  • , Tan Wu
  • , Pascale J.M. Schafrat
  • , Sanne Ten Hoorn
  • , Miaomiao Tan
  • , Lingli He
  • , Sander R. van Hooff
  • , Jan Koster
  • , Lisanne E. Nijman
  • , Geraldine R. Vink
  • , Inès J. Beumer
  • , Clara C. Elbers
  • , Kristiaan J. Lenos
  • , Dirkje W. Sommeijer
  • , Xin Wang
  • , Louis Vermeulen*
  • *Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

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Abstract

Consensus Molecular Subtype (CMS) classification of colorectal cancer (CRC) tissues is complicated by RNA degradation upon formalin-fixed paraffin-embedded (FFPE) preservation. Here, we present an FFPE-curated CMS classifier. The CMSFFPE classifier was developed using genes with a high transcript integrity in FFPE-derived RNA. We evaluated the classification accuracy in two FFPE-RNA datasets with matched fresh-frozen (FF) RNA data, and an FF-derived RNA set. An FFPE-RNA application cohort of metastatic CRC patients was established, partly treated with anti-EGFR therapy. Key characteristics per CMS were assessed. Cross-referenced with matched benchmark FF CMS calls, the CMSFFPE classifier strongly improved classification accuracy in two FFPE datasets compared with the original CMSClassifier (63.6% versus 40.9% and 83.3% versus 66.7%, respectively). We recovered CMS-specific recurrence-free survival patterns (CMS4 versus CMS2: hazard ratio 1.75, 95% CI 1.24–2.46). Key molecular and clinical associations of the CMSs were confirmed. In particular, we demonstrated the predictive value of CMS2 and CMS3 for anti-EGFR therapy response (CMS2&3: odds ratio 5.48, 95% CI 1.10–27.27). The CMSFFPE classifier is an optimized FFPE-curated research tool for CMS classification of clinical CRC samples.

Original languageEnglish
Article numbere202402730
Number of pages17
JournalLife Science Alliance
Volume7
Issue number8
DOIs
Publication statusPublished - Aug 2024

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