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Polymalic Acid-based Nano Biopolymers for Targeting of Multiple Tumor Markers: An Opportunity for Personalized Medicine?
Published on: June 13, 2014
Optimizing treatment for HER2-positive HR-positive breast cancer
Veronique Debien1, Evandro de Azambuja1, Martine Piccart-Gebhart2
1Université Libre de Bruxelles (U.L.B), Hôpital Universitaire de Bruxelles (HUB), Institut Jules Bordet, Academic Trials Promoting Team, Brussels, Belgium.
Abstract:
Triple-positive breast tumors overexpress human epidermal growth factor receptor 2 (HER2) and are positive for hormone receptor (HR) expression. Data from real-life and clinical trials show that estrogen receptor (ER) expression affects the response to combinations of anti-HER2 and associated systemic therapies. Despite triple-positive tumors having decreased response rates compared to HR-negative/HER2-positive breast cancers, optimizing anti-HER2 treatment with dual anti-HER2 blockade remains important for optimal disease control. Preclinical data on the cross-talk between ER and growth factor receptor pathways show the efficacy of combinations of endocrine therapy and anti-HER2 drugs, which is confirmed in the clinic. Molecular dissection of triple-positive breast cancer might provide the rational for additional therapeutic strategies and the identification of promising biomarkers. This review summarizes data on systemic treatment efficacy from major clinical trials and perspectives for future clinical research in triple-positive breast cancer.
Insights
Triple-positive breast cancer, overexpressing HER2 and HR, benefits from dual anti-HER2 blockade and endocrine therapy. Research explores optimizing treatments and identifying biomarkers for better disease control.
Area of Science:
- Oncology
- Breast Cancer Research
Background:
- Triple-positive breast tumors overexpress human epidermal growth factor receptor 2 (HER2) and hormone receptors (HR).
- Estrogen receptor (ER) expression influences treatment response in HER2-positive breast cancers receiving anti-HER2 and systemic therapies.
Purpose of the Study:
- To review systemic treatment efficacy in triple-positive breast cancer from clinical trials.
- To explore future research directions and potential biomarkers for triple-positive breast cancer.
Main Methods:
- Review of clinical trial data on systemic treatment efficacy.
- Analysis of preclinical and clinical data on endocrine therapy and anti-HER2 drug combinations.
Main Results:
- Triple-positive breast cancers show decreased response rates compared to HR-negative/HER2-positive subtypes.
- Combinations of endocrine therapy and anti-HER2 drugs demonstrate clinical efficacy.
- Dual anti-HER2 blockade is crucial for optimal disease control.
Conclusions:
- Optimizing anti-HER2 treatment with dual blockade is vital for triple-positive breast cancer.
- Molecular insights may reveal new therapeutic strategies and biomarkers.
- Further research is needed to refine treatment approaches for this subtype.
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