Human epidermal growth factor receptor targeted inhibitors for the treatment of ovarian cancer
Maria Bonello1, Andrew Harvey Sims1, Simon Peter Langdon1
1Cancer Research UK Edinburgh Center and Division of Pathology Laboratory, MRC Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh, EH4 2XU, UK.
Abstract:
Ovarian cancer is the second most lethal gynecological cancer worldwide and while most patients respond to initial therapy, they often relapse with resistant disease. Human epidermal growth factor receptors (especially HER1/EGFR and HER2/ERBB2) are involved in disease progression; hence, strategies to inhibit their action could prove advantageous in ovarian cancer patients, especially in patients resistant to first line therapy. Monoclonal antibodies and tyrosine kinase inhibitors are two classes of drugs that act on these receptors. They have demonstrated valuable antitumor activity in multiple cancers and their possible use in ovarian cancer continues to be studied. In this review, we discuss the human epidermal growth factor receptor family; review emerging clinical studies on monoclonal antibodies and tyrosine kinase inhibitors targeting these receptors in ovarian cancer patients; and propose future research possibilities in this area.
Insights
Targeting human epidermal growth factor receptors (EGFR, ERBB2) with new drugs offers hope for ovarian cancer patients who relapse. These therapies, including monoclonal antibodies and tyrosine kinase inhibitors, are being studied for resistant disease.
Area of Science:
- Oncology
- Molecular Biology
- Pharmacology
Background:
- Ovarian cancer is a leading cause of cancer death globally.
- Most patients initially respond to treatment but often develop resistant disease, necessitating novel therapeutic strategies.
- The human epidermal growth factor receptor (HER) family, including EGFR and ERBB2, plays a role in ovarian cancer progression.
Purpose of the Study:
- To review the human epidermal growth factor receptor family in the context of ovarian cancer.
- To examine emerging clinical studies on targeted therapies for ovarian cancer.
- To propose future research directions for HER-targeted treatments in ovarian cancer.
Main Methods:
- Literature review of the human epidermal growth factor receptor family.
- Analysis of emerging clinical studies on monoclonal antibodies and tyrosine kinase inhibitors in ovarian cancer.
- Synthesis of current research to identify future therapeutic possibilities.
Main Results:
- Human epidermal growth factor receptors are implicated in ovarian cancer progression and resistance.
- Monoclonal antibodies and tyrosine kinase inhibitors targeting HER receptors show potential in various cancers.
- Clinical studies are exploring the efficacy of these targeted agents in ovarian cancer, particularly in resistant cases.
Conclusions:
- Targeting the human epidermal growth factor receptor family presents a promising avenue for treating ovarian cancer, especially in patients with resistant disease.
- Further clinical investigation of monoclonal antibodies and tyrosine kinase inhibitors is warranted.
- Future research should focus on optimizing these targeted therapies for improved patient outcomes in ovarian cancer.
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