Changes of topoisomerase IIalpha expression in breast tumors after neoadjuvant chemotherapy predicts relapse-free survival

To assess the value of changes in the expression of topoisomerase IIalpha (TopoII) and the proto-oncogene erbB-2 (HER-2) as predictors of relapse-free survival in women with operable breast cancer treated with anthracycline-based neoadjuvant chemotherapy. Seventy-seven patients with primary breast c...

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Veröffentlicht in:Clinical cancer research 2006-03, Vol.12 (5), p.1501
Hauptverfasser: Tinari, Nicola, Lattanzio, Rossano, Natoli, Clara, Cianchetti, Ettore, Angelucci, Domenico, Ricevuto, Enrico, Ficorella, Corrado, Marchetti, Paolo, Alberti, Saverio, Piantelli, Mauro, Iacobelli, Stefano
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container_title Clinical cancer research
container_volume 12
creator Tinari, Nicola
Lattanzio, Rossano
Natoli, Clara
Cianchetti, Ettore
Angelucci, Domenico
Ricevuto, Enrico
Ficorella, Corrado
Marchetti, Paolo
Alberti, Saverio
Piantelli, Mauro
Iacobelli, Stefano
description To assess the value of changes in the expression of topoisomerase IIalpha (TopoII) and the proto-oncogene erbB-2 (HER-2) as predictors of relapse-free survival in women with operable breast cancer treated with anthracycline-based neoadjuvant chemotherapy. Seventy-seven patients with primary breast cancer who had undergone neoadjuvant anthracycline-based chemotherapy were included in the present study. TopoII and HER-2 were measured by immunohistochemistry in prechemotherapy and postchemotherapy (at the time of surgery) tumor specimens, and the value of their changes as predictors of relapse-free survival were evaluated by Kaplan-Meier and Cox proportional hazard regression analyses. Neoadjuvant chemotherapy resulted in a significant reduction in the percentage of cells expressing TopoII (P < 0.0001). No significant change was observed for HER-2. TopoII and HER-2 expression before chemotherapy predicted tumor response to treatment. Changes in TopoII expression after chemotherapy were strongly associated with a poor relapse-free survival (P < 0.0001) in a Cox multivariate analysis adjusted for other clinicopathologic prognostic factors. Changes in TopoII expression after anthracycline-based neoadjuvant chemotherapy is an independent predictor of a poor relapse-free survival in patients with breast cancer. Tumor cells displaying an increased TopoII expression after treatment may be responsible for relapses, and may, therefore, define a group of patients with anthracycline-resistant breast cancer.
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Seventy-seven patients with primary breast cancer who had undergone neoadjuvant anthracycline-based chemotherapy were included in the present study. TopoII and HER-2 were measured by immunohistochemistry in prechemotherapy and postchemotherapy (at the time of surgery) tumor specimens, and the value of their changes as predictors of relapse-free survival were evaluated by Kaplan-Meier and Cox proportional hazard regression analyses. Neoadjuvant chemotherapy resulted in a significant reduction in the percentage of cells expressing TopoII (P &lt; 0.0001). No significant change was observed for HER-2. TopoII and HER-2 expression before chemotherapy predicted tumor response to treatment. Changes in TopoII expression after chemotherapy were strongly associated with a poor relapse-free survival (P &lt; 0.0001) in a Cox multivariate analysis adjusted for other clinicopathologic prognostic factors. Changes in TopoII expression after anthracycline-based neoadjuvant chemotherapy is an independent predictor of a poor relapse-free survival in patients with breast cancer. 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Seventy-seven patients with primary breast cancer who had undergone neoadjuvant anthracycline-based chemotherapy were included in the present study. TopoII and HER-2 were measured by immunohistochemistry in prechemotherapy and postchemotherapy (at the time of surgery) tumor specimens, and the value of their changes as predictors of relapse-free survival were evaluated by Kaplan-Meier and Cox proportional hazard regression analyses. Neoadjuvant chemotherapy resulted in a significant reduction in the percentage of cells expressing TopoII (P &lt; 0.0001). No significant change was observed for HER-2. TopoII and HER-2 expression before chemotherapy predicted tumor response to treatment. Changes in TopoII expression after chemotherapy were strongly associated with a poor relapse-free survival (P &lt; 0.0001) in a Cox multivariate analysis adjusted for other clinicopathologic prognostic factors. 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Seventy-seven patients with primary breast cancer who had undergone neoadjuvant anthracycline-based chemotherapy were included in the present study. TopoII and HER-2 were measured by immunohistochemistry in prechemotherapy and postchemotherapy (at the time of surgery) tumor specimens, and the value of their changes as predictors of relapse-free survival were evaluated by Kaplan-Meier and Cox proportional hazard regression analyses. Neoadjuvant chemotherapy resulted in a significant reduction in the percentage of cells expressing TopoII (P &lt; 0.0001). No significant change was observed for HER-2. TopoII and HER-2 expression before chemotherapy predicted tumor response to treatment. Changes in TopoII expression after chemotherapy were strongly associated with a poor relapse-free survival (P &lt; 0.0001) in a Cox multivariate analysis adjusted for other clinicopathologic prognostic factors. Changes in TopoII expression after anthracycline-based neoadjuvant chemotherapy is an independent predictor of a poor relapse-free survival in patients with breast cancer. Tumor cells displaying an increased TopoII expression after treatment may be responsible for relapses, and may, therefore, define a group of patients with anthracycline-resistant breast cancer.</abstract><cop>United States</cop><pmid>16533774</pmid></addata></record>
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source MEDLINE; American Association for Cancer Research; EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection
subjects Adult
Aged
Antigens, Neoplasm - metabolism
Antineoplastic Combined Chemotherapy Protocols - therapeutic use
Breast Neoplasms - diagnosis
Breast Neoplasms - drug therapy
Breast Neoplasms - metabolism
Cyclophosphamide - therapeutic use
Disease-Free Survival
DNA Topoisomerases, Type II - metabolism
DNA-Binding Proteins - metabolism
Drug Resistance, Neoplasm
Epirubicin - therapeutic use
Female
Fluorouracil - therapeutic use
Humans
Mastectomy
Middle Aged
Neoadjuvant Therapy
Neoplasm Invasiveness - pathology
Neoplasm Recurrence, Local - diagnosis
Neoplasm Recurrence, Local - drug therapy
Neoplasm Recurrence, Local - metabolism
Neoplasm, Residual - drug therapy
Neoplasm, Residual - metabolism
Prognosis
Receptor, ErbB-2 - metabolism
Stereoisomerism
title Changes of topoisomerase IIalpha expression in breast tumors after neoadjuvant chemotherapy predicts relapse-free survival
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