Evidence map›Paper›PMID 40679712›Full record

ArticleBreast cancer research and treatment2025

Quantitative assessment of HER2 expression in invasive ductal carcinoma and co-existing DCIS.

Haiying Zhan, Nay Nwe Nyein Chan, Revekka Khaimova, Thazin N Aung, Patricia Gaule, Charles J Robbins, David L Rimm

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Article in Breast cancer research and treatment, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

7 authors.

Haiying ZhanDepartment of Pathology, Yale School of Medicine, New Haven, CT, 06520, USA. haiying.zhan@yale.edu.
Nay Nwe Nyein ChanDepartment of Pathology, Yale School of Medicine, New Haven, CT, 06520, USA.
Revekka KhaimovaDepartment of Pathology, Yale School of Medicine, New Haven, CT, 06520, USA.
Thazin N AungDepartment of Pathology, Yale School of Medicine, New Haven, CT, 06520, USA.
Patricia GauleDepartment of Pathology, Yale School of Medicine, New Haven, CT, 06520, USA.
Charles J RobbinsDepartment of Pathology, Yale School of Medicine, New Haven, CT, 06520, USA.
David L RimmDepartment of Pathology, Yale School of Medicine, New Haven, CT, 06520, USA.

Funding

Breast Cancer Research Foundation BCRF 23-138
6 · The paper itself

Abstract

purposePrevious studies have demonstrated that ductal carcinoma in situ (DCIS) component often exhibits higher HER2 expression than the invasive component when assessed by immunohistochemistry, while some other studies showed concordant HER2 expression between these two components. In this study, we used our high-sensitivity HER2 (HS-HER2) quantitative immunofluorescence assay to compare HER2 expression in IDC and co-existing DCIS and correlate with clinicopathologic characteristics.

methodsWe included 36 IDC + DCIS cases from the Yale Pathology department. DCIS was classified according to the three-tier nuclear grading system: low (grade 1), intermediate (grade 2), and high (grade 3) nuclear grade. Invasive carcinoma was graded according to the modified Bloom-Richardson histologic grading system. Cases were divided into two groups: low to intermediate-grade DCIS (G1-2) with co-existing invasive carcinoma (n = 26) and high-grade DCIS (G3) with co-existing invasive carcinoma (n = 10). Separate regions of interest for IDC and DCIS were annotated by two board-certified pathologists. Serial sections of FFPE tumor specimens were used to accurately measure the HER2 protein expression by the HS-HER2 assay in attomole/mm

resultsLow to intermediate-grade DCIS expressed higher HER2 levels (4295 ± 449 amol/mm

conclusionUsing the HS-HER2 assay, our results demonstrated comparable HER2 expression levels in DCIS and paired invasive carcinoma regardless of histopathological grade or HER2 immunohistochemical score. These findings contributed to a more nuanced understanding of HER2 biology in early breast carcinogenesis and may inform future biomarker-driven therapeutic strategies.

Indexed as

Biomarkers, TumorBreast NeoplasmsCarcinoma, Ductal, BreastCarcinoma, Intraductal, NoninfiltratingErb-b2 Receptor Tyrosine KinasesAdultAgedFemaleHumansImmunohistochemistryMiddle AgedNeoplasm GradingBiomarkers, TumorERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesDuctal carcinoma in situHigh sensitivity-HER2 (HS-HER2)Invasive ductal carcinomaQuantitative immunofluorescence

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.