Genomic landscape of treatment refractory metastatic colorectal cancer

R L Eefsen1, K S Simonsen1, P Grundtvig1

  • 1Department of Oncology, Herlev Gentofte Hospital, Herlev, Denmark.

Abstract

Insights

Genomic sequencing identified cancer driver mutations in 90% of patients with refractory metastatic colorectal cancer (mCRC). However, only a small fraction received targeted therapy, highlighting a gap in personalized treatment options for mCRC.

Area of Science:

  • Oncology
  • Genomics
  • Personalized Medicine

Background:

  • Metastatic colorectal cancer (mCRC) presents treatment challenges due to its complexity and heterogeneity.
  • Limited standard and targeted therapy options exist for patients with refractory mCRC.
  • Genomic sequencing offers potential for personalized treatment strategies.

Purpose of the Study:

  • To analyze genomic profiles of patients with treatment-refractory mCRC.
  • To identify actionable cancer driver mutations for personalized therapy.
  • To evaluate the feasibility of targeted treatment based on genomic findings.

Main Methods:

  • Retrospective analysis of 80 patients with refractory mCRC referred to the Experimental Cancer Therapy Unit (ECTU).
  • Next-generation sequencing (NGS) of tumor tissue using the Oncomine Comprehensive primer panel.
  • Detection of actionable variants, microsatellite instability, and tumor mutational burden.

Main Results:

  • Cancer driver mutations were identified in 90% of patients.
  • 31.3% of patients received therapy, including targeted, FDA-approved, or phase 1/2 trial treatments.
  • Only 2.5% of patients received targeted therapy matched to their genomic mutations.

Conclusions:

  • The majority of refractory mCRC patients harbor actionable cancer driver mutations.
  • A significant gap exists between identified mutations and the availability of matched targeted therapies.
  • Personalized treatment strategies for mCRC require further development to bridge this gap.

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