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Updated: Mar 8, 2026

Studying Triple Negative Breast Cancer Using Orthotopic Breast Cancer Model
Published on: March 20, 2020
Targeting Epidermal Growth Factor Receptor in triple negative breast cancer: New discoveries and practical insights
Ricardo Costa1, Ami N Shah2, Cesar A Santa-Maria3
1Developmental Therapeutics Program, Division of Hematology/Oncology, Feinberg School of Medicine, Chicago, USA.
Abstract:
Triple negative breast cancer (TNBC) accounts for 10-20% of cases in breast cancer. Despite recent advances in the treatment of hormonal receptor+ and HER2+ breast cancers, there are no targeted therapies available for TNBC. Evidence supports that most patients with TNBC express the transmembrane Epidermal Growth Factor Receptor (EGFR). However, early phase clinical trials failed to demonstrate significant activity of EGFR-targeted monoclonal antibodies and/or tyrosine kinase inhibitors. Here, we review the recent discoveries related to the underlying biology of the EGFR pathway in TNBC, clinical progress to date and suggest rational future approaches for investigational therapies in TNBC.
Insights
Triple negative breast cancer (TNBC) lacks targeted therapies, despite EGFR expression in most patients. This review explores EGFR pathway biology, clinical trials, and future therapeutic strategies for TNBC.
Area of Science:
- Oncology
- Molecular Biology
- Cancer Therapeutics
Background:
- Triple negative breast cancer (TNBC) represents 10-20% of all breast cancer cases.
- TNBC lacks targeted therapies, unlike hormone receptor-positive and HER2-positive breast cancers.
- Most TNBC tumors express the Epidermal Growth Factor Receptor (EGFR).
Purpose of the Study:
- To review recent discoveries in EGFR pathway biology specific to TNBC.
- To summarize the clinical progress of EGFR-targeted therapies in TNBC.
- To propose rational future investigational therapeutic approaches for TNBC.
Main Methods:
- Literature review of recent discoveries in EGFR pathway biology.
- Analysis of clinical trial data for EGFR-targeted agents in TNBC.
- Synthesis of current knowledge to suggest future therapeutic strategies.
Main Results:
- Early clinical trials of EGFR-targeted monoclonal antibodies and tyrosine kinase inhibitors showed limited success in TNBC.
- The underlying biology of the EGFR pathway in TNBC is complex and requires further elucidation.
- Despite challenges, the EGFR pathway remains a potential target for novel TNBC therapies.
Conclusions:
- Targeted therapies for TNBC are urgently needed.
- Further research into the EGFR pathway's role in TNBC is crucial.
- Developing novel therapeutic strategies targeting the EGFR pathway holds promise for improving TNBC treatment outcomes.
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