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Clinical and microarray analysis of breast cancers of all subtypes from two prospective preoperative chemotherapy studies

BACKGROUND: We aimed to analyse clinical and gene expression profiles to predict pathologic complete response and disease-free survival using two consecutive, prospective, preoperative chemotherapy trial cohorts. METHODS: Clinicopathological and gene expression data were evaluated in a cohort from t...

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Autores principales: Okuma, H S, Koizumi, F, Hirakawa, A, Nakatochi, M, Komori, O, Hashimoto, J, Kodaira, M, Yunokawa, M, Yamamoto, H, Yonemori, K, Shimizu, C, Fujiwara, Y, Tamura, K
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4985347/
https://www.ncbi.nlm.nih.gov/pubmed/27415010
http://dx.doi.org/10.1038/bjc.2016.184
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author Okuma, H S
Koizumi, F
Hirakawa, A
Nakatochi, M
Komori, O
Hashimoto, J
Kodaira, M
Yunokawa, M
Yamamoto, H
Yonemori, K
Shimizu, C
Fujiwara, Y
Tamura, K
author_facet Okuma, H S
Koizumi, F
Hirakawa, A
Nakatochi, M
Komori, O
Hashimoto, J
Kodaira, M
Yunokawa, M
Yamamoto, H
Yonemori, K
Shimizu, C
Fujiwara, Y
Tamura, K
author_sort Okuma, H S
collection PubMed
description BACKGROUND: We aimed to analyse clinical and gene expression profiles to predict pathologic complete response and disease-free survival using two consecutive, prospective, preoperative chemotherapy trial cohorts. METHODS: Clinicopathological and gene expression data were evaluated in a cohort from two consecutive phase II preoperative studies that included patients with stage IIA–IIIC breast cancer of all subtypes. Analysed specimens were obtained before preoperative chemotherapy, and cDNA microarray analyses were performed using the Affymetrix Gene Chip U133 plus 2.0. RESULTS: Between December 2005 and December 2010, 122 patients were analysed. The pathologic complete response rate was significantly higher in HER2+ and HR−/HER2− cancers. Age, pathologic complete response, HR−/HER2− status, and lymph node positivity (⩾4) were significant poor prognostic factors for disease-free survival. For the cDNA microarray analyses, sufficient tumour samples were available from 78 of the 107 patients (73%). An 8-gene signature predictive of pathologic complete response and a 17-gene signature predictive of prognosis were identified. Patients were categorised into low-risk (n=45) and high-risk groups (n=33) (HR 70.0, P=0.004). CONCLUSIONS: This study yielded preliminary data on the expression of specific genes predicting pathologic complete response and disease-free survival in a cohort of chemonaïve breast cancer patients. Further validation may distinguish those who would benefit most from perioperative chemotherapy as well as those needing further intervention.
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spelling pubmed-49853472016-08-29 Clinical and microarray analysis of breast cancers of all subtypes from two prospective preoperative chemotherapy studies Okuma, H S Koizumi, F Hirakawa, A Nakatochi, M Komori, O Hashimoto, J Kodaira, M Yunokawa, M Yamamoto, H Yonemori, K Shimizu, C Fujiwara, Y Tamura, K Br J Cancer Clinical Study BACKGROUND: We aimed to analyse clinical and gene expression profiles to predict pathologic complete response and disease-free survival using two consecutive, prospective, preoperative chemotherapy trial cohorts. METHODS: Clinicopathological and gene expression data were evaluated in a cohort from two consecutive phase II preoperative studies that included patients with stage IIA–IIIC breast cancer of all subtypes. Analysed specimens were obtained before preoperative chemotherapy, and cDNA microarray analyses were performed using the Affymetrix Gene Chip U133 plus 2.0. RESULTS: Between December 2005 and December 2010, 122 patients were analysed. The pathologic complete response rate was significantly higher in HER2+ and HR−/HER2− cancers. Age, pathologic complete response, HR−/HER2− status, and lymph node positivity (⩾4) were significant poor prognostic factors for disease-free survival. For the cDNA microarray analyses, sufficient tumour samples were available from 78 of the 107 patients (73%). An 8-gene signature predictive of pathologic complete response and a 17-gene signature predictive of prognosis were identified. Patients were categorised into low-risk (n=45) and high-risk groups (n=33) (HR 70.0, P=0.004). CONCLUSIONS: This study yielded preliminary data on the expression of specific genes predicting pathologic complete response and disease-free survival in a cohort of chemonaïve breast cancer patients. Further validation may distinguish those who would benefit most from perioperative chemotherapy as well as those needing further intervention. Nature Publishing Group 2016-08-09 2016-07-14 /pmc/articles/PMC4985347/ /pubmed/27415010 http://dx.doi.org/10.1038/bjc.2016.184 Text en Copyright © 2016 Cancer Research UK http://creativecommons.org/licenses/by-nc-sa/4.0/ This work is licensed under the Creative Commons Attribution-Non-Commercial-Share Alike 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/
spellingShingle Clinical Study
Okuma, H S
Koizumi, F
Hirakawa, A
Nakatochi, M
Komori, O
Hashimoto, J
Kodaira, M
Yunokawa, M
Yamamoto, H
Yonemori, K
Shimizu, C
Fujiwara, Y
Tamura, K
Clinical and microarray analysis of breast cancers of all subtypes from two prospective preoperative chemotherapy studies
title Clinical and microarray analysis of breast cancers of all subtypes from two prospective preoperative chemotherapy studies
title_full Clinical and microarray analysis of breast cancers of all subtypes from two prospective preoperative chemotherapy studies
title_fullStr Clinical and microarray analysis of breast cancers of all subtypes from two prospective preoperative chemotherapy studies
title_full_unstemmed Clinical and microarray analysis of breast cancers of all subtypes from two prospective preoperative chemotherapy studies
title_short Clinical and microarray analysis of breast cancers of all subtypes from two prospective preoperative chemotherapy studies
title_sort clinical and microarray analysis of breast cancers of all subtypes from two prospective preoperative chemotherapy studies
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4985347/
https://www.ncbi.nlm.nih.gov/pubmed/27415010
http://dx.doi.org/10.1038/bjc.2016.184
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