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Standardizing Pathologic Evaluation of Breast Carcinoma After Neoadjuvant Chemotherapy
Sunati Sahoo1, Gregor Krings2, Yunn-Yi Chen2
1From the Department of Pathology, UTSW Medical Center, Dallas, Texas (Sahoo).
Neoadjuvant systemic therapy for breast cancer requires standardized pathology reporting. This review addresses challenges in evaluating post-treatment specimens and suggests improvements for staging systems like the American Joint Committee on Cancer and Residual Cancer Burden.
Area of Science:
- Pathology
- Oncology
- Breast Cancer Research
Background:
- Neoadjuvant systemic therapy is increasingly used for breast cancer before surgery.
- Evaluation of post-neoadjuvant breast cancer specimens lacks a universal reporting protocol.
- Current staging systems face challenges in assessing residual tumor burden accurately.
Purpose of the Study:
- To offer guidance for evaluating and reporting post-neoadjuvant breast specimens.
- To discuss limitations of existing staging and reporting systems.
- To propose modifications for the American Joint Committee on Cancer staging and Residual Cancer Burden calculator.
Main Methods:
- Literature review of English-language publications.
- Analysis of data from the I-SPY 2 neoadjuvant clinical trial.
Main Results:
- Identified challenges in the pathologic evaluation of treated breast carcinomas.
- Highlighted the need for standardized reporting protocols.
- Emphasized the utility of the Residual Cancer Burden system for quantifying treatment response.
Conclusions:
- Pathologic evaluation of post-neoadjuvant breast cancer specimens requires clear guidelines.
- Recommendations are provided for pathologists and clinicians.
- Future modifications to staging systems are suggested to improve residual tumor burden assessment.
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