What is a breast panel?

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Last updated: November 24, 2025View editorial policy

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What is a Breast Panel?

A "breast panel" refers to the comprehensive set of biomarker tests performed on breast tissue specimens to determine tumor hormone receptor status (estrogen receptor/progesterone receptor [ER/PR]) and HER2 status, which are essential for guiding treatment decisions in breast cancer. 1

Core Components of the Breast Panel

The breast panel includes testing for three critical biomarkers:

  • Estrogen Receptor (ER) status - determines if the tumor responds to estrogen and predicts response to endocrine therapy 1
  • Progesterone Receptor (PR) status - provides additional information about hormone sensitivity and treatment response 1
  • HER2 status - identifies tumors that overexpress HER2 protein, which predicts response to HER2-targeted therapies like trastuzumab 1

When the Breast Panel is Performed

All patients with newly diagnosed invasive breast cancer must have determination of ER/PR and HER2 status as part of their initial pathologic assessment. 1

The panel is performed on tissue obtained from:

  • Core needle biopsy of the primary breast tumor (preferred initial method) 1
  • Surgical excision specimens if core biopsy was not performed 1
  • Lymph node biopsies when metastatic disease is present 1

Clinical Significance

These biomarkers are not merely prognostic—they are predictive factors that directly determine treatment selection:

  • ER/PR-positive tumors (approximately 70% of breast cancers) are treated with endocrine therapy (tamoxifen, aromatase inhibitors) 1
  • HER2-positive tumors (approximately 15-20% of breast cancers) receive HER2-targeted therapy such as trastuzumab or pertuzumab 1
  • Triple-negative tumors (ER-negative, PR-negative, HER2-negative) require chemotherapy as the primary systemic treatment 1

Standardized Reporting Requirements

The College of American Pathologists (CAP) protocols must be used for all breast cancer pathology reporting, including the breast panel results. 1

This standardization is critical because:

  • National surveys show up to 50% of breast cancer pathology reports are missing critical elements needed for treatment decisions 1
  • Incomplete reporting can lead to inappropriate treatment selection and worse outcomes 1
  • The CAP protocols ensure consistent, complete documentation of all biomarkers 1

Common Pitfalls to Avoid

  • Failing to test all three markers - some providers may omit PR testing if ER is positive, but PR status provides independent prognostic information 1
  • Not obtaining adequate tissue - insufficient tissue from fine-needle aspiration may preclude complete biomarker testing; core biopsy is preferred 1
  • Delaying treatment while awaiting results - the breast panel should be ordered immediately upon diagnosis, as results typically take 3-5 days and are required before initiating systemic therapy 1

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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