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Pathologic complete response of ductal carcinoma in situ to neoadjuvant systemic therapy in HER2-positive invasive breast cancer patients: a nationwide analysis

PURPOSE: Ductal carcinoma in situ (DCIS) is present in more than half of HER2-positive invasive breast cancer (IBC). Recent studies show that DCIS accompanying HER2-positive IBC can be completely eradicated by neoadjuvant systemic therapy (NST). Our aim was to determine the percentage of pathologic...

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Autores principales: Ploumen, Roxanne A. W., Claassens, Eva L., Kooreman, Loes F. S., Keymeulen, Kristien B. M. I., van Kats, Maartje A. C. E., Gommers, Suzanne, Siesling, Sabine, van Nijnatten, Thiemo J. A., Smidt, Marjolein L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10361905/
https://www.ncbi.nlm.nih.gov/pubmed/37395816
http://dx.doi.org/10.1007/s10549-023-07012-z
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author Ploumen, Roxanne A. W.
Claassens, Eva L.
Kooreman, Loes F. S.
Keymeulen, Kristien B. M. I.
van Kats, Maartje A. C. E.
Gommers, Suzanne
Siesling, Sabine
van Nijnatten, Thiemo J. A.
Smidt, Marjolein L.
author_facet Ploumen, Roxanne A. W.
Claassens, Eva L.
Kooreman, Loes F. S.
Keymeulen, Kristien B. M. I.
van Kats, Maartje A. C. E.
Gommers, Suzanne
Siesling, Sabine
van Nijnatten, Thiemo J. A.
Smidt, Marjolein L.
author_sort Ploumen, Roxanne A. W.
collection PubMed
description PURPOSE: Ductal carcinoma in situ (DCIS) is present in more than half of HER2-positive invasive breast cancer (IBC). Recent studies show that DCIS accompanying HER2-positive IBC can be completely eradicated by neoadjuvant systemic therapy (NST). Our aim was to determine the percentage of pathologic complete response of the DCIS component in a nationwide cohort and to assess associated clinicopathologic variables. Furthermore, the impact on surgical treatment after NST was investigated. METHODS: Women diagnosed with HER2-positive IBC, treated with NST and surgery, between 2010 and 2020, were selected from the Netherlands Cancer Registry. Pre-NST biopsy and postoperative pathology reports were obtained from the Dutch Nationwide Pathology Databank and assessed for the presence of DCIS. Clinicopathologic factors associated with DCIS response were assessed using logistic regression analyses. RESULTS: A DCIS component was present in the pre-NST biopsy in 1403 (25.1%) of 5598 included patients. Pathologic complete response of the DCIS component was achieved in 730 patients (52.0%). Complete response of DCIS occurred more frequently in case of complete response of IBC (63.4% versus 33.8%, p < 0.001). ER-negative IBC (OR 1.79; 95%CI 1.33–2.42) and more recent years of diagnosis (2014–2016 OR 1.60; 95%CI 1.17–2.19, 2017–2019 OR 1.76; 95%CI 1.34–2.34) were associated with DCIS response. Mastectomy rates were higher in IBC+DCIS compared to IBC (53.6% versus 41.0%, p < 0.001). CONCLUSION: Pathologic complete response of DCIS occurred in 52.0% of HER2-positive IBC patients and was associated with ER-negative IBC and more recent years of diagnosis. Future studies should investigate imaging evaluation of DCIS response to improve surgical decision making. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10549-023-07012-z.
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spelling pubmed-103619052023-07-23 Pathologic complete response of ductal carcinoma in situ to neoadjuvant systemic therapy in HER2-positive invasive breast cancer patients: a nationwide analysis Ploumen, Roxanne A. W. Claassens, Eva L. Kooreman, Loes F. S. Keymeulen, Kristien B. M. I. van Kats, Maartje A. C. E. Gommers, Suzanne Siesling, Sabine van Nijnatten, Thiemo J. A. Smidt, Marjolein L. Breast Cancer Res Treat Clinical Trial PURPOSE: Ductal carcinoma in situ (DCIS) is present in more than half of HER2-positive invasive breast cancer (IBC). Recent studies show that DCIS accompanying HER2-positive IBC can be completely eradicated by neoadjuvant systemic therapy (NST). Our aim was to determine the percentage of pathologic complete response of the DCIS component in a nationwide cohort and to assess associated clinicopathologic variables. Furthermore, the impact on surgical treatment after NST was investigated. METHODS: Women diagnosed with HER2-positive IBC, treated with NST and surgery, between 2010 and 2020, were selected from the Netherlands Cancer Registry. Pre-NST biopsy and postoperative pathology reports were obtained from the Dutch Nationwide Pathology Databank and assessed for the presence of DCIS. Clinicopathologic factors associated with DCIS response were assessed using logistic regression analyses. RESULTS: A DCIS component was present in the pre-NST biopsy in 1403 (25.1%) of 5598 included patients. Pathologic complete response of the DCIS component was achieved in 730 patients (52.0%). Complete response of DCIS occurred more frequently in case of complete response of IBC (63.4% versus 33.8%, p < 0.001). ER-negative IBC (OR 1.79; 95%CI 1.33–2.42) and more recent years of diagnosis (2014–2016 OR 1.60; 95%CI 1.17–2.19, 2017–2019 OR 1.76; 95%CI 1.34–2.34) were associated with DCIS response. Mastectomy rates were higher in IBC+DCIS compared to IBC (53.6% versus 41.0%, p < 0.001). CONCLUSION: Pathologic complete response of DCIS occurred in 52.0% of HER2-positive IBC patients and was associated with ER-negative IBC and more recent years of diagnosis. Future studies should investigate imaging evaluation of DCIS response to improve surgical decision making. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10549-023-07012-z. Springer US 2023-07-03 2023 /pmc/articles/PMC10361905/ /pubmed/37395816 http://dx.doi.org/10.1007/s10549-023-07012-z Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Clinical Trial
Ploumen, Roxanne A. W.
Claassens, Eva L.
Kooreman, Loes F. S.
Keymeulen, Kristien B. M. I.
van Kats, Maartje A. C. E.
Gommers, Suzanne
Siesling, Sabine
van Nijnatten, Thiemo J. A.
Smidt, Marjolein L.
Pathologic complete response of ductal carcinoma in situ to neoadjuvant systemic therapy in HER2-positive invasive breast cancer patients: a nationwide analysis
title Pathologic complete response of ductal carcinoma in situ to neoadjuvant systemic therapy in HER2-positive invasive breast cancer patients: a nationwide analysis
title_full Pathologic complete response of ductal carcinoma in situ to neoadjuvant systemic therapy in HER2-positive invasive breast cancer patients: a nationwide analysis
title_fullStr Pathologic complete response of ductal carcinoma in situ to neoadjuvant systemic therapy in HER2-positive invasive breast cancer patients: a nationwide analysis
title_full_unstemmed Pathologic complete response of ductal carcinoma in situ to neoadjuvant systemic therapy in HER2-positive invasive breast cancer patients: a nationwide analysis
title_short Pathologic complete response of ductal carcinoma in situ to neoadjuvant systemic therapy in HER2-positive invasive breast cancer patients: a nationwide analysis
title_sort pathologic complete response of ductal carcinoma in situ to neoadjuvant systemic therapy in her2-positive invasive breast cancer patients: a nationwide analysis
topic Clinical Trial
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10361905/
https://www.ncbi.nlm.nih.gov/pubmed/37395816
http://dx.doi.org/10.1007/s10549-023-07012-z
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