Is the 21-Gene Recurrence Score on Core Needle Biopsy Equivalent to Surgical Specimen in Early-Stage Breast Cancer? A Comparison of Gene Expression Between Paired Core Needle Biopsy and Surgical Specimens

Background Molecular testing on surgical specimens predicts disease recurrence and benefit of adjuvant chemotherapy in hormone receptor-positive (HR+), human epidermal growth factor receptor 2-negative (HER2−) early-stage breast cancer (EBC). Testing on core biopsies has become common practice despi...

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Veröffentlicht in:Annals of surgical oncology 2021-10, Vol.28 (10), p.5588-5596
Hauptverfasser: Orozco, Javier I. J., Chang, Shu-Ching, Matsuba, Chikako, Ensenyat-Mendez, Miquel, Grunkemeier, Gary L., Marzese, Diego M., Grumley, Janie G.
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Sprache:eng
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Zusammenfassung:Background Molecular testing on surgical specimens predicts disease recurrence and benefit of adjuvant chemotherapy in hormone receptor-positive (HR+), human epidermal growth factor receptor 2-negative (HER2−) early-stage breast cancer (EBC). Testing on core biopsies has become common practice despite limited evidence of concordance between core/surgical samples. In this study, we compared the gene expression of the 21 genes and the recurrence score (RS) between paired core/surgical specimens. Methods Eighty patients with HR+/HER2− EBC were evaluated from two publicly available gene expression datasets (GSE73235, GSE76728) with paired core/surgical specimens without neoadjuvant systemic therapy. The expression of the 21 genes was compared in paired samples. A microarray-based RS was calculated and a value ≥ 26 was defined as high-RS. The concordance rate and kappa statistic were used to evaluate the agreement between the RS of paired samples. Results Overall, there was no significant difference and a high correlation in the gene expression levels of the 21 genes between paired samples. However, CD68 and RPLP0 in GSE73235, AURKA , BAG1 , and TFRC in GSE76728, and MYLBL2 and ACTB in both datasets exhibited weak to moderate correlation ( r  
ISSN:1068-9265
1534-4681
DOI:10.1245/s10434-021-10457-5