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An Overview of Clinical Development of Agents for Metastatic or Advanced Breast Cancer Without ERBB2 Amplification
Aleix Prat1,2,3, Aditya Bardia4, Giuseppe Curigliano5,6
1Department of Medical Oncology, Hospital Clinic of Barcelona, Barcelona, Spain.
Importance:
Erb-b2 receptor tyrosine kinase 2 (ERBB2; formerly HER2 [human epidermal growth factor receptor 2]) is an important prognostic and predictive factor in breast cancer. Anti-ERBB2 therapies have improved outcomes in ERBB2-positive breast cancer. However, based on current definitions, tumors with low ERBB2 expression are included in the ERBB2-negative subtype, and therefore, are ineligible for anti-ERBB2 therapies; patients with ERBB2-low (immunohistochemistry [IHC] 1 positive [+] or IHC 2+/in situ hybridization [ISH] negative [-]) tumors account for up to approximately 50% of breast cancer cases. Although the prognostic role of ERBB2-low needs to be defined, ERBB2 offers a potential therapeutic target in these patients.
Observations:
Most breast cancer tumors have some ERBB2 expression, with ERBB2-low being more common in hormone receptor-positive than in hormone receptor-negative breast cancer. Although an early clinical study failed to demonstrate benefit of adjuvant trastuzumab for ERBB2-low disease, several novel anti-ERBB2 therapies have shown efficacy in ERBB2-low breast cancer, including the antibody-drug conjugate trastuzumab deruxtecan in a phase 3 trial, and trastuzumab duocarmazine and the bispecific antibody zenocutuzumab in early-phase studies. Although reports are conflicting, some differences in biology and patient outcomes have been found between ERBB2-low and ERBB2 IHC-0 breast cancer. Currently, no established guidelines exist for scoring ERBB2-low expression in breast cancer because the focus has been on binary classification as ERBB2-positive or ERBB2-negative. Additional interpretive cutoffs may be needed to select patients for treatment with effective agents in ERBB2-low breast cancer, along with standardized laboratory quality assurance programs to ensure consistent patient identification for eligibility for ERBB2-low targeting agents.
Conclusions And Relevance:
This review suggests that ERBB2-low may be a distinct, clinically relevant breast cancer entity warranting reassessment of traditional diagnostic and therapeutic paradigms. Ongoing clinical trials and further investigations may provide optimized strategies for diagnosing and treating ERBB2-low breast cancer, including reproducible, consistent definitions to identify patients in this diagnostic category and demonstration of benefits of emerging therapies.
Insights
ERBB2-low breast cancer, comprising up to 50% of cases, represents a distinct subtype. Emerging therapies show promise for ERBB2-low patients, necessitating new diagnostic criteria for targeted treatment.
Area of Science:
- Oncology
- Molecular Biology
- Clinical Pathology
Background:
- Erb-b2 receptor tyrosine kinase 2 (ERBB2) is a key factor in breast cancer prognosis and treatment.
- Current definitions exclude ERBB2-low tumors (IHC 1+ or IHC 2+/ISH-) from anti-ERBB2 therapies, despite their prevalence (up to 50% of cases).
- ERBB2-low breast cancer is more common in hormone receptor-positive disease.
Purpose of the Study:
- To review the clinical relevance of ERBB2-low breast cancer.
- To discuss the potential of ERBB2 as a therapeutic target in ERBB2-low breast cancer.
- To highlight the need for revised diagnostic and therapeutic strategies.
Main Methods:
- Review of existing literature on ERBB2 expression in breast cancer.
- Analysis of clinical trial data for novel anti-ERBB2 therapies in ERBB2-low breast cancer.
- Discussion of diagnostic scoring and quality assurance for ERBB2-low identification.
Main Results:
- Several novel anti-ERBB2 therapies, including trastuzumab deruxtecan, demonstrate efficacy in ERBB2-low breast cancer.
- Conflicting reports exist regarding biological and outcome differences between ERBB2-low and ERBB2 IHC-0 breast cancer.
- Current diagnostic guidelines lack specific cutoffs for ERBB2-low expression.
Conclusions:
- ERBB2-low breast cancer may represent a distinct clinical entity requiring reassessment of current paradigms.
- Optimized diagnostic strategies and standardized quality assurance are crucial for patient selection.
- Ongoing trials are expected to provide further insights into effective treatments for ERBB2-low breast cancer.
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