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Clinical utility of the IHC4+C score in oestrogen receptor-positive early breast cancer: a prospective decision impact study

BACKGROUND: Most oestrogen receptor (ER)-positive early breast cancer diagnosed today is highly curable with multimodality treatment. Systemic adjuvant treatments including endocrine therapy and chemotherapy have made a significant contribution to the increasing cure rates over the past three decade...

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Autores principales: Yeo, B, Zabaglo, L, Hills, M, Dodson, A, Smith, I, Dowsett, M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4522631/
https://www.ncbi.nlm.nih.gov/pubmed/26180920
http://dx.doi.org/10.1038/bjc.2015.222
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author Yeo, B
Zabaglo, L
Hills, M
Dodson, A
Smith, I
Dowsett, M
author_facet Yeo, B
Zabaglo, L
Hills, M
Dodson, A
Smith, I
Dowsett, M
author_sort Yeo, B
collection PubMed
description BACKGROUND: Most oestrogen receptor (ER)-positive early breast cancer diagnosed today is highly curable with multimodality treatment. Systemic adjuvant treatments including endocrine therapy and chemotherapy have made a significant contribution to the increasing cure rates over the past three decades. However not all women will require chemotherapy. The IHC4+C score is a prognostic tool that integrates four immunohistochemical measures with clinicopathological features to estimate the residual risk of distant recurrence at 10 years in post-menopausal women with ER-positive breast cancer who have received 5 years of endocrine therapy. Retrospective studies indicate that the test can identify a set of women that are at such low risk of recurrence that chemotherapy can be of little benefit. METHODS: In this study, 124 patients were prospectively selected from the multidisciplinary team meeting between January 2013 and April 2014 for IHC4+C testing. Adjuvant systemic treatment recommendations by clinicians were recorded without and with the availability of the score in addition to the patient's decision. RESULTS: There was concordance in the MDT's recommendation without and with the availability of the score in 73% of cases. Clinicians recommended chemotherapy or at least its discussion to 74 (59%) patients, which fell to 32 (34%) patients after the IHC4+C score was made available, sparing one in four tested patients a chemotherapy recommendation, along with its toxicity and expense. CONCLUSION: This decision impact study shows that when used by clinicians in the multidisciplinary team meeting for adjuvant decision-making, a significant proportion of patients are spared chemotherapy recommendations.
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spelling pubmed-45226312016-07-28 Clinical utility of the IHC4+C score in oestrogen receptor-positive early breast cancer: a prospective decision impact study Yeo, B Zabaglo, L Hills, M Dodson, A Smith, I Dowsett, M Br J Cancer Clinical Study BACKGROUND: Most oestrogen receptor (ER)-positive early breast cancer diagnosed today is highly curable with multimodality treatment. Systemic adjuvant treatments including endocrine therapy and chemotherapy have made a significant contribution to the increasing cure rates over the past three decades. However not all women will require chemotherapy. The IHC4+C score is a prognostic tool that integrates four immunohistochemical measures with clinicopathological features to estimate the residual risk of distant recurrence at 10 years in post-menopausal women with ER-positive breast cancer who have received 5 years of endocrine therapy. Retrospective studies indicate that the test can identify a set of women that are at such low risk of recurrence that chemotherapy can be of little benefit. METHODS: In this study, 124 patients were prospectively selected from the multidisciplinary team meeting between January 2013 and April 2014 for IHC4+C testing. Adjuvant systemic treatment recommendations by clinicians were recorded without and with the availability of the score in addition to the patient's decision. RESULTS: There was concordance in the MDT's recommendation without and with the availability of the score in 73% of cases. Clinicians recommended chemotherapy or at least its discussion to 74 (59%) patients, which fell to 32 (34%) patients after the IHC4+C score was made available, sparing one in four tested patients a chemotherapy recommendation, along with its toxicity and expense. CONCLUSION: This decision impact study shows that when used by clinicians in the multidisciplinary team meeting for adjuvant decision-making, a significant proportion of patients are spared chemotherapy recommendations. Nature Publishing Group 2015-07-28 2015-07-16 /pmc/articles/PMC4522631/ /pubmed/26180920 http://dx.doi.org/10.1038/bjc.2015.222 Text en Copyright © 2015 Cancer Research UK http://creativecommons.org/licenses/by-nc-sa/4.0/ From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 4.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/
spellingShingle Clinical Study
Yeo, B
Zabaglo, L
Hills, M
Dodson, A
Smith, I
Dowsett, M
Clinical utility of the IHC4+C score in oestrogen receptor-positive early breast cancer: a prospective decision impact study
title Clinical utility of the IHC4+C score in oestrogen receptor-positive early breast cancer: a prospective decision impact study
title_full Clinical utility of the IHC4+C score in oestrogen receptor-positive early breast cancer: a prospective decision impact study
title_fullStr Clinical utility of the IHC4+C score in oestrogen receptor-positive early breast cancer: a prospective decision impact study
title_full_unstemmed Clinical utility of the IHC4+C score in oestrogen receptor-positive early breast cancer: a prospective decision impact study
title_short Clinical utility of the IHC4+C score in oestrogen receptor-positive early breast cancer: a prospective decision impact study
title_sort clinical utility of the ihc4+c score in oestrogen receptor-positive early breast cancer: a prospective decision impact study
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4522631/
https://www.ncbi.nlm.nih.gov/pubmed/26180920
http://dx.doi.org/10.1038/bjc.2015.222
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