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Published on: August 1, 2018
The Relationships between HER2 Overexpression and DCIS Characteristics
Pamela Di Cesare1, Lorenzo Pavesi2, Laura Villani2
1Department of Medical Oncology, Humanitas Mater Domini Hospital, Castellanza, Italy.
Human epidermal growth factor receptor 2 (HER2) overexpression in ductal carcinoma in situ (DCIS) is linked to younger patients and higher recurrence risk. HER2-positive DCIS correlates with poor prognostic factors, suggesting its utility in treatment decisions.
Area of Science:
- Oncology
- Pathology
- Genetics
Background:
- Ductal carcinoma in situ (DCIS) is a non-invasive breast cancer precursor.
- HER2 overexpression is a known factor in invasive breast cancer prognosis.
- The prognostic significance of HER2 in DCIS requires further elucidation.
Purpose of the Study:
- To investigate the correlation between HER2 overexpression and prognostic factors in DCIS.
- To assess the recurrence risk associated with HER2 status in DCIS patients.
- To determine if HER2 testing can guide treatment decisions for DCIS.
Main Methods:
- Evaluation of 48 DCIS cases based on HER2 amplification status.
- Immunohistochemistry used to assess HER2, Ki67, estrogen receptor (ER), and progesterone receptor (PgR) expression.
- Histopathological variables including nuclear grade and "cancerization of lobules" were analyzed.
- Comparison of recurrence risk factors between HER2-positive and HER2-negative DCIS groups.
Main Results:
- HER2-positive DCIS was significantly associated with younger patient age (p = 0.002).
- HER2-positive DCIS correlated with adverse prognostic factors: high nuclear grade (p < 0.001), high Ki67 (p = 0.003), low ER/PgR (p < 0.001), and "cancerization of lobules" (p = 0.049).
- A high risk of recurrence was hypothesized for HER2-positive DCIS.
Conclusions:
- HER2 amplification in DCIS is more frequent in younger patients.
- HER2-positive DCIS is associated with histopathological predictors of recurrence.
- HER2 testing in DCIS may aid clinicians in selecting optimal patient treatments.
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