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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
Molecular mechanisms and targeting of colorectal cancer
1Department of Medicine, Medical Oncology and Hematology, Gastroenterology, and Infectious Disease, Marienkrankenhaus, Hamburg, Germany. vanhoefer.innere@marienkrankenhaus.org
Abstract:
Targeted therapies that are approved for metastatic colorectal cancer are divided into two groups: those affecting vascular endothelial growth factor (VEGF) known to interrupt tumor growth and metastasis (also called neo-angiogenesis), and agents that affect the tumor directly by interrupting the epidermal growth factor (EGF) and its receptor. Anti-angiogenic VEGF therapies are divided into two categories: one affecting the VEGF ligand, such as bevacizumab, and those that inhibit the VEGF receptor, such as PTK/ZK. Epidermal growth factor receptor (EGFR) therapies are divided into monoclonal antibodies that affect EGFR, such as cetuximab, and EGFR tyrosine kinase inhibitors, such as gefitinib. Both VEGF and EGFR areas of treatment have shown promising efficacy in first-line, combination therapy settings. Future targeted therapeutic strategies include gene profiling, combinations of capecitabine and oxaliplatin, with bevacizumab and/or cetuximab therapies.
Insights
Targeted therapies for metastatic colorectal cancer focus on inhibiting vascular endothelial growth factor (VEGF) or epidermal growth factor (EGF) pathways. These treatments show promise in combination therapies and future strategies involve gene profiling and drug combinations.
Area of Science:
- Oncology
- Pharmacology
- Molecular Biology
Background:
- Metastatic colorectal cancer (mCRC) treatment has advanced with targeted therapies.
- Current targeted agents focus on two main pathways: vascular endothelial growth factor (VEGF) and epidermal growth factor receptor (EGFR).
Purpose of the Study:
- To review approved targeted therapies for mCRC.
- To categorize therapies based on their molecular targets (VEGF or EGFR).
- To discuss the efficacy of these agents in combination settings and future therapeutic directions.
Main Methods:
- Literature review of approved targeted therapies for mCRC.
- Classification of therapies based on their mechanism of action (VEGF ligand/receptor inhibition, EGFR inhibition).
- Summary of clinical efficacy in first-line and combination settings.
Main Results:
- Targeted therapies for mCRC are grouped into anti-VEGF and anti-EGFR agents.
- Anti-VEGF therapies include ligand inhibitors (e.g., bevacizumab) and receptor inhibitors (e.g., PTK/ZK).
- Anti-EGFR therapies include monoclonal antibodies (e.g., cetuximab) and tyrosine kinase inhibitors (e.g., gefitinib).
- Both VEGF and EGFR-targeted therapies demonstrate efficacy in first-line and combination treatments.
Conclusions:
- VEGF and EGFR targeted therapies are crucial in managing metastatic colorectal cancer.
- Combination strategies and gene profiling are promising future directions for mCRC treatment.
- Future research may involve combining chemotherapy (capecitabine, oxaliplatin) with targeted agents like bevacizumab and cetuximab.
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