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Retrospective observational study of HER2 immunohistochemistry in borderline breast cancer patients undergoing neoadjuvant therapy, with an emphasis on Group 2 (HER2/CEP17 ratio ≥2.0, HER2 copy number <4.0 signals/cell) cases

BACKGROUND: The ASCO/CAP guidance on HER2 testing in breast cancer (BC) has recently changed. Group 2 tumours with immunohistochemistry score 2+ and HER2/CEP17 ratio ≥2.0 and HER2 copy number <4.0 signals/cell were re-classified as HER2 negative. This study aims to examine the response of Group 2...

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Autores principales: Rakha, Emad A., Miligy, Islam M., Quinn, Cecily M., Provenzano, Elena, Shaaban, Abeer M., Marchiò, Caterina, Toss, Michael S., Gallagy, Grace, Murray, Ciara, Walshe, Janice, Katayama, Ayaka, Eldib, Karim, Badr, Nahla, Tanchel, Bruce, Millican-Slater, Rebecca, Purdie, Colin, Purnell, Dave, Pinder, Sarah E., Ellis, Ian O., Lee, Andrew H. S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8144199/
https://www.ncbi.nlm.nih.gov/pubmed/33762723
http://dx.doi.org/10.1038/s41416-021-01351-8
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author Rakha, Emad A.
Miligy, Islam M.
Quinn, Cecily M.
Provenzano, Elena
Shaaban, Abeer M.
Marchiò, Caterina
Toss, Michael S.
Gallagy, Grace
Murray, Ciara
Walshe, Janice
Katayama, Ayaka
Eldib, Karim
Badr, Nahla
Tanchel, Bruce
Millican-Slater, Rebecca
Purdie, Colin
Purnell, Dave
Pinder, Sarah E.
Ellis, Ian O.
Lee, Andrew H. S.
author_facet Rakha, Emad A.
Miligy, Islam M.
Quinn, Cecily M.
Provenzano, Elena
Shaaban, Abeer M.
Marchiò, Caterina
Toss, Michael S.
Gallagy, Grace
Murray, Ciara
Walshe, Janice
Katayama, Ayaka
Eldib, Karim
Badr, Nahla
Tanchel, Bruce
Millican-Slater, Rebecca
Purdie, Colin
Purnell, Dave
Pinder, Sarah E.
Ellis, Ian O.
Lee, Andrew H. S.
author_sort Rakha, Emad A.
collection PubMed
description BACKGROUND: The ASCO/CAP guidance on HER2 testing in breast cancer (BC) has recently changed. Group 2 tumours with immunohistochemistry score 2+ and HER2/CEP17 ratio ≥2.0 and HER2 copy number <4.0 signals/cell were re-classified as HER2 negative. This study aims to examine the response of Group 2 tumours to neoadjuvant chemotherapy (NACT). METHODS: 749 BC cases were identified from 11 institutions. The association between HER2 groups and pathological complete response (pCR) was assessed. RESULTS: 54% of immunohistochemistry HER2 positive (score 3+) BCs showed pCR, compared to 19% of immunohistochemistry 2+ FISH amplified cases. 27% of Group 2 treated with HER2 targeted therapy achieved pCR, compared to 19 and 11% in the combined Groups 1 + 3 and Groups 4 + 5, respectively. No difference in pCR rates was identified between Group 2 and Group 1 or combined Groups 1 + 3. However, Group 2 response rate was higher than Groups 4 + 5 (p = 0.017). CONCLUSION: No difference in pCR was detected in tumours with a HER2/CEP17 ratio ≥2.0 and a HER2 score 2+ by IHC when stratified by HER2 gene copy number. Our data suggest that ASCO/CAP HER2 Group 2 carcinomas should be evaluated further with respect to eligibility for HER2 targeted therapy.
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spelling pubmed-81441992021-06-07 Retrospective observational study of HER2 immunohistochemistry in borderline breast cancer patients undergoing neoadjuvant therapy, with an emphasis on Group 2 (HER2/CEP17 ratio ≥2.0, HER2 copy number <4.0 signals/cell) cases Rakha, Emad A. Miligy, Islam M. Quinn, Cecily M. Provenzano, Elena Shaaban, Abeer M. Marchiò, Caterina Toss, Michael S. Gallagy, Grace Murray, Ciara Walshe, Janice Katayama, Ayaka Eldib, Karim Badr, Nahla Tanchel, Bruce Millican-Slater, Rebecca Purdie, Colin Purnell, Dave Pinder, Sarah E. Ellis, Ian O. Lee, Andrew H. S. Br J Cancer Article BACKGROUND: The ASCO/CAP guidance on HER2 testing in breast cancer (BC) has recently changed. Group 2 tumours with immunohistochemistry score 2+ and HER2/CEP17 ratio ≥2.0 and HER2 copy number <4.0 signals/cell were re-classified as HER2 negative. This study aims to examine the response of Group 2 tumours to neoadjuvant chemotherapy (NACT). METHODS: 749 BC cases were identified from 11 institutions. The association between HER2 groups and pathological complete response (pCR) was assessed. RESULTS: 54% of immunohistochemistry HER2 positive (score 3+) BCs showed pCR, compared to 19% of immunohistochemistry 2+ FISH amplified cases. 27% of Group 2 treated with HER2 targeted therapy achieved pCR, compared to 19 and 11% in the combined Groups 1 + 3 and Groups 4 + 5, respectively. No difference in pCR rates was identified between Group 2 and Group 1 or combined Groups 1 + 3. However, Group 2 response rate was higher than Groups 4 + 5 (p = 0.017). CONCLUSION: No difference in pCR was detected in tumours with a HER2/CEP17 ratio ≥2.0 and a HER2 score 2+ by IHC when stratified by HER2 gene copy number. Our data suggest that ASCO/CAP HER2 Group 2 carcinomas should be evaluated further with respect to eligibility for HER2 targeted therapy. Nature Publishing Group UK 2021-03-24 2021-05-25 /pmc/articles/PMC8144199/ /pubmed/33762723 http://dx.doi.org/10.1038/s41416-021-01351-8 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Rakha, Emad A.
Miligy, Islam M.
Quinn, Cecily M.
Provenzano, Elena
Shaaban, Abeer M.
Marchiò, Caterina
Toss, Michael S.
Gallagy, Grace
Murray, Ciara
Walshe, Janice
Katayama, Ayaka
Eldib, Karim
Badr, Nahla
Tanchel, Bruce
Millican-Slater, Rebecca
Purdie, Colin
Purnell, Dave
Pinder, Sarah E.
Ellis, Ian O.
Lee, Andrew H. S.
Retrospective observational study of HER2 immunohistochemistry in borderline breast cancer patients undergoing neoadjuvant therapy, with an emphasis on Group 2 (HER2/CEP17 ratio ≥2.0, HER2 copy number <4.0 signals/cell) cases
title Retrospective observational study of HER2 immunohistochemistry in borderline breast cancer patients undergoing neoadjuvant therapy, with an emphasis on Group 2 (HER2/CEP17 ratio ≥2.0, HER2 copy number <4.0 signals/cell) cases
title_full Retrospective observational study of HER2 immunohistochemistry in borderline breast cancer patients undergoing neoadjuvant therapy, with an emphasis on Group 2 (HER2/CEP17 ratio ≥2.0, HER2 copy number <4.0 signals/cell) cases
title_fullStr Retrospective observational study of HER2 immunohistochemistry in borderline breast cancer patients undergoing neoadjuvant therapy, with an emphasis on Group 2 (HER2/CEP17 ratio ≥2.0, HER2 copy number <4.0 signals/cell) cases
title_full_unstemmed Retrospective observational study of HER2 immunohistochemistry in borderline breast cancer patients undergoing neoadjuvant therapy, with an emphasis on Group 2 (HER2/CEP17 ratio ≥2.0, HER2 copy number <4.0 signals/cell) cases
title_short Retrospective observational study of HER2 immunohistochemistry in borderline breast cancer patients undergoing neoadjuvant therapy, with an emphasis on Group 2 (HER2/CEP17 ratio ≥2.0, HER2 copy number <4.0 signals/cell) cases
title_sort retrospective observational study of her2 immunohistochemistry in borderline breast cancer patients undergoing neoadjuvant therapy, with an emphasis on group 2 (her2/cep17 ratio ≥2.0, her2 copy number <4.0 signals/cell) cases
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8144199/
https://www.ncbi.nlm.nih.gov/pubmed/33762723
http://dx.doi.org/10.1038/s41416-021-01351-8
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