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.

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.