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Development and Maintenance of a Preclinical Patient Derived Tumor Xenograft Model for the Investigation of Novel Anti-Cancer Therapies
Published on: September 30, 2016
Addressing Challenges in Targeted Therapy for Metastatic Colorectal Cancer
Maria El Hage1, Zhaoran Su1, Michael Linnebacher1
1Molecular Oncology and Immunotherapy, Clinic of General Surgery, Rostock University Medical Center, 18057 Rostock, Germany.
Abstract:
This review article aims to address the challenges associated with targeted therapy for the treatment of metastatic colorectal cancer (mCRC). We will first provide an overview of approved targeted therapies for treating mCRC, which include antiangiogenic therapy, as well as inhibitors of EGFR, BRAFV600E, HER2 inhibitors, and immune checkpoints. Second, we discuss the different mechanisms of primary resistance, including tumor heterogeneity, both as inter-patient and intra-patient heterogeneity, and mechanisms of secondary resistance which include: driver oncogene alterations, downstream or parallel bypass signaling, presence of co-dominant driver oncogenes, tumor lineage plasticity, and epithelial to mesenchymal transition. Resistance mechanisms towards the different drug classes targeting mCRC are discussed in detail. Strategies to overcome resistance primarily involve combination of therapies, although this approach is typically linked to increased drug toxicity, manifesting as on and off-target effects. Moreover, the cost and accessibility of targeted therapies pose significant challenges for diverse populations. Addressing these challenges necessitates further research efforts aimed at optimizing the use of targeted therapy in mCRC. Integration of genomic biomarkers, such as sequencing and liquid biopsy, into routine clinical practice holds promise in enhancing treatment outcomes. In conclusion, this comprehensive review underscores the complex challenges encountered in targeted therapy for mCRC.
Insights
Targeted therapy for metastatic colorectal cancer (mCRC) faces challenges from primary and secondary resistance mechanisms. Overcoming these requires combination therapies and genomic biomarkers for optimized treatment outcomes.
Area of Science:
- Oncology
- Pharmacology
- Genetics
Background:
- Metastatic colorectal cancer (mCRC) treatment relies on targeted therapies.
- Approved therapies include antiangiogenic agents, EGFR, BRAFV600E, HER2 inhibitors, and immune checkpoints.
- Resistance to these therapies is a significant clinical challenge.
Purpose of the Study:
- To review approved targeted therapies for mCRC.
- To discuss primary and secondary resistance mechanisms.
- To explore strategies for overcoming resistance and improving treatment outcomes.
Main Methods:
- Literature review of targeted therapies for mCRC.
- Analysis of resistance mechanisms, including tumor heterogeneity and genetic alterations.
- Discussion of combination therapy strategies and genomic biomarker integration.
Main Results:
- Multiple targeted therapies are available for mCRC.
- Primary resistance mechanisms include tumor heterogeneity.
- Secondary resistance involves driver oncogene alterations, bypass signaling, co-dominant oncogenes, lineage plasticity, and epithelial-mesenchymal transition.
- Combination therapies can increase toxicity.
- Cost and accessibility are significant barriers.
Conclusions:
- Targeted therapy for mCRC is complex due to resistance mechanisms.
- Combination therapies and genomic biomarkers (sequencing, liquid biopsy) are promising strategies.
- Further research is needed to optimize targeted therapy use and address accessibility issues.
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