Surgical specimen can be replaced by core samples in assessment of ER, PR and HER-2 for invasive breast cancer.
Author(s): Sutela A, Vanninen R, Sudah M, Berg M, Kiviniemi V, Rummukainen J, Kataja V, Kärjä V
Publication: Acta Oncol, 2008, Vol. 47, Page 38-46
PubMed ID: 17851859 PubMed Review Paper? No
Purpose of Paper
Conclusion of Paper
Studies
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Study Purpose
The purpose of this study was to compare IHC staining of ER, PR and HER-2 in SCNB and surgical specimens from breast carcinomas. SCNB from the tumor center versus 2 mm away were also compared.
Summary of Findings:
Concordance between IHC staining of surgical specimens and SCNB was observed in 83% of cases for ER, and 88% of cases for PR and HER-2, and 93% of cases if HER-2 ISH was also performed. The false negative rate from surgical specimens was 14% for ER, 15% for PR and 7% for HER-2 (when ISH was included). In contrast, false negatives in SCNB did not occur for PR and HER-2 (with ISH) and occurred in only 6% of specimens for ER. The center and margins of the tumor were concordant 100% of the time for ER but only 85% of the time for PR and HER-2. The use of three core specimens for IHC staining allowed for 95% sensitivity for ER, and 92% for PR and HER-2, however, the sensitivity increased to 100% for HER-2 if ISH was also used. The addition of further specimens did not increase ER sensitivity, but did increase sensitivity of PR to 100%. In conclusion, SCNB were more sensitive than surgical specimens for ER, PR, and HER-2 staining, but it was necessary to analyze multiple SCNB.
Biospecimens
Preservative Types
- Formalin
Diagnoses:
- Neoplastic - Carcinoma
Platform:
Analyte Technology Platform Protein Immunohistochemistry DNA In situ hybridization Morphology H-and-E microscopy Pre-analytical Factors:
Classification Pre-analytical Factor Value(s) Immunohistochemistry Specific Targeted peptide/protein Estrogen receptor
Progesterone receptor
Human epidermal growth-factor receptor
In situ hybridization Specific Targeted nucleic acid Human epidermal growth-factor receptor
Biospecimen Aliquots and Components Biospecimen heterogeneity Biospecimen core
Biospecimen periphery
Biospecimen Acquisition Method of tissue acquisition Core needle biopsy
Surgical resection