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Updated: May 15, 2025

Validated Immunochemical Assay for Comprehensive Determination of the Human Epidermal Growth Factor Receptor 2 Released from and Bound to Cells
Published on: May 9, 2025
Incidence, Clinicopathologic Features, and Follow-Up Results of human epidermal growth factor receptor-2-Ultralow
Yan Hu1, Daniel Jones1, Weiqiang Zhao1
1Department of Pathology, The Ohio State University Wexner Medical Center, Columbus, Ohio.
Abstract:
The preliminary result of DESTINY-Breast06 trial demonstrated the effectiveness of antibody-drug conjugate in patients with human epidermal growth factor receptor-2 (HER2)-ultralow breast carcinoma (BC), defined by the presence of ≤10% of infiltrating cancer cells showing incomplete and faint/weak membrane staining on HER2 immunohistochemistry. In this study, we investigated the pathologic features and clinical outcomes in patients with HER2-ultralow, HER2-null, and HER2-low expression. The incidence of HER2 ultralow was 17.5% (260/1486). The incidence of other groups is as follows: 7.7% for HER2 null, 56.8% for HER2 low, and 18% for HER2 positive. HER2-ultralow cases showed similarity to HER2-low cases but a significant difference from HER2-null cases, including older age (61.1 vs 57.3 years; P = .0099), fewer grade 3 BCs (18.1% vs 53.9%; P < .0001), triple-negative BCs (16.2% vs 42.6%; P < .0001), estrogen receptor (ER)-negative BCs (16.5% vs 47.8%; P < .0001), and progesterone receptor-negative BCs (26.2% vs 54.8%; P < .0001). When cases were stratified based on ER positivity, these differences between HER2-null and HER2-ultralow groups were confined to ER+ but not ER- cases. There were no discernible differences in response to neoadjuvant chemotherapy (n = 125) among HER2-null, HER2-ultralow, and HER2-low BCs. HER2-null/ER-BCs displayed a lower probability of overall survival than HER2-ultralow and HER2-low/ER-BCs, but no statistically significant difference was observed in disease-free survival among the 3 groups. HER2-ultralow BCs exhibit distinct features that align more closely with HER2-low BCs than HER2-null BCs. These findings contribute to the evolving classification of HER2 expression in BC and may have implications for refining treatment strategies in this subgroup.
Insights
Human epidermal growth factor receptor-2 (HER2)-ultralow breast cancer (BC) shares features with HER2-low BC, not HER2-null BC. This finding aids in classifying HER2 expression and refining treatment strategies for HER2-ultralow BC.
Area of Science:
- Oncology
- Pathology
- Genetics
Background:
- The DESTINY-Breast06 trial highlighted antibody-drug conjugate efficacy in HER2-ultralow breast carcinoma (BC).
- HER2-ultralow BC is defined by ≤10% of cancer cells with incomplete/faint membrane staining on HER2 immunohistochemistry.
- Understanding HER2-ultralow BC's distinct characteristics is crucial for treatment stratification.
Purpose of the Study:
- To investigate the pathologic features and clinical outcomes of HER2-ultralow BC.
- To compare HER2-ultralow BC with HER2-null and HER2-low BC subtypes.
- To inform the evolving classification and treatment strategies for HER2-expressing breast cancers.
Main Methods:
- Retrospective analysis of patient data including pathologic features and clinical outcomes.
- Classification of breast cancer cases into HER2-null, HER2-ultralow, HER2-low, and HER2-positive groups.
- Statistical comparison of demographic, pathologic, and survival data across HER2 expression groups.
Main Results:
- HER2-ultralow BC (17.5% incidence) showed similarities to HER2-low BC but differed significantly from HER2-null BC.
- HER2-ultralow BC cases were associated with older age, fewer grade 3 tumors, and lower rates of triple-negative, ER-negative, and PR-negative status compared to HER2-null BC.
- No significant differences in neoadjuvant chemotherapy response were observed among HER2-null, HER2-ultralow, and HER2-low BCs.
Conclusions:
- HER2-ultralow breast cancer exhibits distinct pathologic and clinical features that align more closely with HER2-low BC.
- These findings support refining the classification of HER2 expression in breast cancer.
- The distinct profile of HER2-ultralow BC may necessitate tailored treatment strategies.

