Targeted therapy in advanced metastatic colorectal cancer: current concepts and perspectives

Florian Hohla1, Thomas Winder1, Richard Greil1

  • 1Florian Hohla, Richard Greil, III Medical Department with Hematology, Medical Oncology, Hemostasis, Rheumatology and Infectious Diseases, Oncologic Center, Center for Clinical Cancer and Immunology Trials, Laboratory of Immunological and Molecular Cancer Research, Paracelsus Medical University of Salzburg, A-5020 Salzburg, Austria.

Insights

New treatments targeting vascular endothelial growth factor (VEGF) and epidermal growth factor receptor (EGFR) have improved outcomes for metastatic colorectal cancer (mCRC). However, resistance necessitates novel strategies, including targeting GI peptides and growth factors implicated in CRC progression.

Area of Science:

  • Oncology
  • Molecular Biology
  • Clinical Research

Background:

  • Metastatic colorectal cancer (mCRC) treatments have advanced with cytotoxic agents and targeted therapies.
  • Vascular Endothelial Growth Factor (VEGF) and Epidermal Growth Factor Receptor (EGFR) signaling inhibitors have improved clinical outcomes in mCRC.
  • Treatment resistance and disease progression remain significant challenges in mCRC management.

Purpose of the Study:

  • To review current clinical data on VEGF and EGFR targeting regimens in mCRC.
  • To explore novel therapeutic strategies targeting peptide receptors and growth factors implicated in CRC growth.
  • To summarize experimental investigations of antagonistic analogs and cytotoxic peptides for CRC treatment.

Main Methods:

  • Comprehensive literature review of clinical trials and experimental studies.
  • Analysis of data on VEGF and EGFR targeting agents in mCRC.
  • Summary of research on GI peptides, growth factors, and neuropeptides in CRC.
  • Review of experimental data on peptide-based therapies for CRC.

Main Results:

  • VEGF and EGFR targeting therapies offer temporary benefits in mCRC, often followed by resistance.
  • Several GI peptides (gastrin, GRP), growth factors (IGF-I, IGF-II), and neuropeptides (GHRH) are implicated in CRC growth.
  • Experimental approaches using antagonistic analogs and targeted cytotoxic peptides show promise for CRC treatment.

Conclusions:

  • Despite advances, resistance to current mCRC therapies necessitates the development of new treatment strategies.
  • Targeting peptide receptors with specific analogs and cytotoxic peptides represents a promising avenue for future CRC therapies.
  • Further research into the role of GI peptides and growth factors could unveil new therapeutic targets for mCRC.

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