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Molecular characterization of breast cancer needle core biopsy specimens by the 21‐gene Breast Recurrence Score test

BACKGROUND AND OBJECTIVE: Recent COVID‐19 pandemic guidelines recommend genomic assessment of core biopsies to help guide treatment decisions in estrogen receptor (ER)‐positive early‐stage breast cancer. Herein we characterize biopsy and excisional breast cancer specimens submitted for 21‐gene testi...

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Autores principales: Jakubowski, Debbie M., Bailey, Helen, Abran, John, Blacklock, Andrea, Ciau, Nancy, Mies, Carolyn, Tan, Vivian, Young, Rebekah, Lau, Anna, Baehner, Frederick L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7496790/
https://www.ncbi.nlm.nih.gov/pubmed/32497318
http://dx.doi.org/10.1002/jso.26050
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author Jakubowski, Debbie M.
Bailey, Helen
Abran, John
Blacklock, Andrea
Ciau, Nancy
Mies, Carolyn
Tan, Vivian
Young, Rebekah
Lau, Anna
Baehner, Frederick L.
author_facet Jakubowski, Debbie M.
Bailey, Helen
Abran, John
Blacklock, Andrea
Ciau, Nancy
Mies, Carolyn
Tan, Vivian
Young, Rebekah
Lau, Anna
Baehner, Frederick L.
author_sort Jakubowski, Debbie M.
collection PubMed
description BACKGROUND AND OBJECTIVE: Recent COVID‐19 pandemic guidelines recommend genomic assessment of core biopsies to help guide treatment decisions in estrogen receptor (ER)‐positive early‐stage breast cancer. Herein we characterize biopsy and excisional breast cancer specimens submitted for 21‐gene testing. METHODS: US samples submitted to Genomic Health for 21‐gene testing (01/2004‐04/2020) were assessed by pathologists and analyzed by a standardized quantitative reverse transcription‐polymerase chain reaction. Predefined cutoffs were: ESR1 (positive ≥6.5), PGR (positive ≥5.5), and ERBB2 (negative <10.7). ER status by immunohistochemistry (IHC) and lymph node status were determined locally. Median and interquartile range were reported for continuous variables, and total and percent for categorical variables. Distributions were assessed overall, by age, and by nodal involvement. RESULTS: Of 919 701 samples analyzed, 13% were biopsies and 87% were excisions. Initial assay success rates were 94.5% (biopsies) and 97.3% (excisions). ER IHC concordance with central ESR1 was 96.8% (biopsies) and 97.6% (excisions). Biopsy and excisional medians were: Recurrence Score results 16 (each); ESR1 10.2 (each); PGR 7.7 and 7.6; ERBB2 9.4 and 9.2, respectively. CONCLUSIONS: Biopsy submissions for 21‐gene testing are common and consistently generate results that are very similar to the experience with excisions. The 21‐gene test can be performed reliably on core biopsies.
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spelling pubmed-74967902020-09-25 Molecular characterization of breast cancer needle core biopsy specimens by the 21‐gene Breast Recurrence Score test Jakubowski, Debbie M. Bailey, Helen Abran, John Blacklock, Andrea Ciau, Nancy Mies, Carolyn Tan, Vivian Young, Rebekah Lau, Anna Baehner, Frederick L. J Surg Oncol Research Articles BACKGROUND AND OBJECTIVE: Recent COVID‐19 pandemic guidelines recommend genomic assessment of core biopsies to help guide treatment decisions in estrogen receptor (ER)‐positive early‐stage breast cancer. Herein we characterize biopsy and excisional breast cancer specimens submitted for 21‐gene testing. METHODS: US samples submitted to Genomic Health for 21‐gene testing (01/2004‐04/2020) were assessed by pathologists and analyzed by a standardized quantitative reverse transcription‐polymerase chain reaction. Predefined cutoffs were: ESR1 (positive ≥6.5), PGR (positive ≥5.5), and ERBB2 (negative <10.7). ER status by immunohistochemistry (IHC) and lymph node status were determined locally. Median and interquartile range were reported for continuous variables, and total and percent for categorical variables. Distributions were assessed overall, by age, and by nodal involvement. RESULTS: Of 919 701 samples analyzed, 13% were biopsies and 87% were excisions. Initial assay success rates were 94.5% (biopsies) and 97.3% (excisions). ER IHC concordance with central ESR1 was 96.8% (biopsies) and 97.6% (excisions). Biopsy and excisional medians were: Recurrence Score results 16 (each); ESR1 10.2 (each); PGR 7.7 and 7.6; ERBB2 9.4 and 9.2, respectively. CONCLUSIONS: Biopsy submissions for 21‐gene testing are common and consistently generate results that are very similar to the experience with excisions. The 21‐gene test can be performed reliably on core biopsies. John Wiley and Sons Inc. 2020-06-04 2020-09-15 /pmc/articles/PMC7496790/ /pubmed/32497318 http://dx.doi.org/10.1002/jso.26050 Text en © 2020 The Authors. Journal of Surgical Oncology published by Wiley Periodicals LLC This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Jakubowski, Debbie M.
Bailey, Helen
Abran, John
Blacklock, Andrea
Ciau, Nancy
Mies, Carolyn
Tan, Vivian
Young, Rebekah
Lau, Anna
Baehner, Frederick L.
Molecular characterization of breast cancer needle core biopsy specimens by the 21‐gene Breast Recurrence Score test
title Molecular characterization of breast cancer needle core biopsy specimens by the 21‐gene Breast Recurrence Score test
title_full Molecular characterization of breast cancer needle core biopsy specimens by the 21‐gene Breast Recurrence Score test
title_fullStr Molecular characterization of breast cancer needle core biopsy specimens by the 21‐gene Breast Recurrence Score test
title_full_unstemmed Molecular characterization of breast cancer needle core biopsy specimens by the 21‐gene Breast Recurrence Score test
title_short Molecular characterization of breast cancer needle core biopsy specimens by the 21‐gene Breast Recurrence Score test
title_sort molecular characterization of breast cancer needle core biopsy specimens by the 21‐gene breast recurrence score test
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7496790/
https://www.ncbi.nlm.nih.gov/pubmed/32497318
http://dx.doi.org/10.1002/jso.26050
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