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Updated: Oct 18, 2025

Development and Maintenance of a Preclinical Patient Derived Tumor Xenograft Model for the Investigation of Novel Anti-Cancer Therapies
Published on: September 30, 2016
Genomic landscape of treatment refractory metastatic colorectal cancer
R L Eefsen1, K S Simonsen1, P Grundtvig1
1Department of Oncology, Herlev Gentofte Hospital, Herlev, Denmark.
Background:
Metastatic colorectal cancer (mCRC) is a complex and heterogeneous disease with few standard and targeted treatment options. Next-generation sequencing of tumor tissue was performed to identify cancer driver mutations to discover possible personalized treatment options, as targeted treatment possibilities are limited for this patient population. Results of genomic sequencing in patients with treatment-refractory mCRC are described in this retrospective analysis.
Material And Methods:
Clinico-pathological characteristics and genomic sequence results of consecutive patients with refractory mCRC, referred to the Experimental Cancer Therapy Unit (ECTU) at Department of Oncology, Herlev & Gentofte Hospital in the period from 1 October 2015 to 14 December 2018 were reviewed in this retrospective analysis. Tumor tissue from the patients was analyzed by next-generation sequencing using the Oncomine Comprehensive primer panel to detect actionable variants of cancer driver mutations and microsatellite instability status. From August 2018 tumor mutational burden was also analyzed.
Results:
A total of 80 patients with treatment-refractory mCRC and in a fairly good performance were referred to the ECTU during this period. Genomic sequencing of tumor tissue was performed for all 80 patients and a cancer driver mutation was identified in 90% (n = 72) of the patients. A total of 31.3% (n = 25) of the patients received therapy either as targetable therapy outside an available trial (n = 2), FDA approved therapy (n = 2), or treatment in phase 1 or 2 trials, independent of the genomic signature 26.3% (n = 21).
Conclusion:
Most mCRC patients refractory to standard anti-neoplastic therapies, presented with a cancer driver mutation, however, only a few of these mutations gave rise to matched therapies as only 2.5% of the patients from this period received targeted therapy.
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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