Receptor de estrogênio beta como marcador preditivo de resposta no tratamento neoadjuvante do carcinoma de mama com anastrozol e tamoxifeno

Detalhes bibliográficos
Autor(a) principal: Madeira, Marcelo [UNIFESP]
Data de Publicação: 2014
Tipo de documento: Tese
Idioma: por
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: https://sucupira.capes.gov.br/sucupira/public/consultas/coleta/trabalhoConclusao/viewTrabalhoConclusao.jsf?popup=true&id_trabalho=1775900
https://repositorio.unifesp.br/handle/11600/46388
Resumo: Background: The role of estrogen receptor beta (ER-β) in breast cancer (BC) remains unclear. Some studies have suggested that ER-β may oppose the actions of estrogen receptor alpha (ER-α), and clinical evidence has indicated that the loss of ER-β expression is associated with a poor prognosis and resistance to endocrine therapy. The objective of the present study is to determine the role of ER-β and the ER-α/ER-β ratio in predicting the response to endocrine therapy and whether different regimens have any effect on ER-β expression levels. Methods: Ninety postmenopausal patients with primary BC were recruited for a short-term double-blinded randomized prospective controlled study. To determine tumor cell proliferation, the expression of Ki67 was measured in tumor biopsy samples taken before and after 26 days of treatment with anastrozole 1 mg/day (N = 25), tamoxifen 20 mg/day (N = 24) or placebo (N = 29) of 78 participants. The pre- and post-samples were placed in tissue microarray blocks and submitted immunohistochemical assay. Biomarker statuses (ER-β, ER-α and Ki67) were obtained by comparing each immunohistochemical evaluation of the pre- and post-surgery samples using the semi-quantitative Allred´s method. Statistical analyses were performed using an ANOVA and Spearman´s correlation coefficient tests, with significance at p ≤ 0.05. Results: The frequency of ER-β expression did not change after treatment (p = 0.33). There were no significant changes in Ki67 levels in ER-β-negative cases (p = 0.45), but in the ER-β-positive cases, the anastrozole (p = 0.01) and tamoxifen groups (p = 0.04) presented a significant reduction in post-treatment Ki67 scores. There was a weak but positive correlation between the ER-α and ER-β expression levels. Only patients with an ER-α/ER-β expression ratio between 1 and 1.5 demonstrated significant differences in Ki67 levels after treatment with anastrozole (p = 0.005) and tamoxifen (p = 0.026). Conclusions: These results provide additional data that indicate that the measurement of ER-β in BC patients may help predict tamoxifen and anastrozole responsiveness in the neoadjuvant setting. These effects of hormonal treatment appear to be dependent on the ratio of ER-α/ER-β expression.
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spelling Receptor de estrogênio beta como marcador preditivo de resposta no tratamento neoadjuvante do carcinoma de mama com anastrozol e tamoxifenoEstrogen receptor alpha/beta ratio and estrogen receptor beta as predictors of endocrine therapy responsiveness–a randomized neoadjuvant trial comparison between anastrozole and tamoxifen for the treatment of postmenopausal breast cancercancerestrogen receptor betareceptor de estrogênio betareceptor de estrogênio alfacâncer de mamatamoxifenoinibidores da aromataseterapia neoadjuvanteBackground: The role of estrogen receptor beta (ER-β) in breast cancer (BC) remains unclear. Some studies have suggested that ER-β may oppose the actions of estrogen receptor alpha (ER-α), and clinical evidence has indicated that the loss of ER-β expression is associated with a poor prognosis and resistance to endocrine therapy. The objective of the present study is to determine the role of ER-β and the ER-α/ER-β ratio in predicting the response to endocrine therapy and whether different regimens have any effect on ER-β expression levels. Methods: Ninety postmenopausal patients with primary BC were recruited for a short-term double-blinded randomized prospective controlled study. To determine tumor cell proliferation, the expression of Ki67 was measured in tumor biopsy samples taken before and after 26 days of treatment with anastrozole 1 mg/day (N = 25), tamoxifen 20 mg/day (N = 24) or placebo (N = 29) of 78 participants. The pre- and post-samples were placed in tissue microarray blocks and submitted immunohistochemical assay. Biomarker statuses (ER-β, ER-α and Ki67) were obtained by comparing each immunohistochemical evaluation of the pre- and post-surgery samples using the semi-quantitative Allred´s method. Statistical analyses were performed using an ANOVA and Spearman´s correlation coefficient tests, with significance at p ≤ 0.05. Results: The frequency of ER-β expression did not change after treatment (p = 0.33). There were no significant changes in Ki67 levels in ER-β-negative cases (p = 0.45), but in the ER-β-positive cases, the anastrozole (p = 0.01) and tamoxifen groups (p = 0.04) presented a significant reduction in post-treatment Ki67 scores. There was a weak but positive correlation between the ER-α and ER-β expression levels. Only patients with an ER-α/ER-β expression ratio between 1 and 1.5 demonstrated significant differences in Ki67 levels after treatment with anastrozole (p = 0.005) and tamoxifen (p = 0.026). Conclusions: These results provide additional data that indicate that the measurement of ER-β in BC patients may help predict tamoxifen and anastrozole responsiveness in the neoadjuvant setting. These effects of hormonal treatment appear to be dependent on the ratio of ER-α/ER-β expression.Introdução: O papel do receptor de estrogênio beta (RE-β) no carcinoma de mama ainda não está esclarecido. Alguns estudos têm sugerido que o RE-β pode apresentar ações opostas ao receptor de estrogênio alfa (RE-α), e evidências clínicas indicaram que a perda de expressão do RE-β está associada a pior prognóstico e resistência à terapia endócrina. O objetivo do presente estudo é determinar o papel do RE-β e da razão de proporção RE-α/RE-β como marcadores preditivos de resposta à endocrinoterapia de curta duração do carcinoma de mama tratado com anastrozol e tamoxifeno e se os diferentes regimes de tratamento têm algum efeito sobre os níveis de expressão do RE-β. Métodos: Noventa pacientes na pós-menopausa com carcinoma primário de mama foram recrutadas para um estudo prospectivo neoadjuvante de curta duração, randomizado, duplo-cego e placebo-controlado. Para determinar o índice de proliferação das células tumorais, a expressão de Ki67 foi avaliada em amostras de biópsias antes e depois de 26 dias de tratamento com anastrozol 1 mg / dia (n = 25), tamoxifeno 20 mg / dia (n = 24) ou placebo (n = 29) nas 78 participantes finais. As amostras obtidas nas biópsias prévias e após tratamentos foram dispostas em blocos de tissue microarray e coradas por imunoistoquímica. A avaliação dos biomarcadores (RE-β, RE-α e Ki67) foi feita de forma semiquantitativa pelo escore de Allred. As análises estatísticas foram realizadas utilizando-se ANOVA e o teste de coeficiente de correlação de Spearman, com significância de p ≤ 0,05. Resultados: A expressão do RE-β não variou após tratamento (p = 0,33). Não houve alterações significativas nos níveis de Ki67 nos casos negativos para RE-β (p = 0,45), mas nos casos positivos, os grupos tratados com anastrozol (p = 0,01) e tamoxifeno (p = 0,04) apresentaram redução significativa na proliferação celular após exposição às drogas. Houve correlação fraca, mas positiva entre os níveis de expressão do RE-α e do RE-β. Somente as pacientes com razão de proporção de expressão RE-α/RE-β entre 1 e 1,5 demonstraram diferenças significativas nos níveis de Ki67 após o tratamento com anastrozol (p = 0,005) e tamoxifeno (p = 0,026). Conclusões: Estes resultados fornecem dados adicionais que indicam que a avaliação neoadjuvante do RE-β em pacientes com carcinoma de mama pode ajudar a prever a resposta ao tratamento com tamoxifeno e anastrozol. Estes efeitos da terapia endócrina do carcinoma de mama parecem ser dependentes da proporção de expressão RE-α/RE-β.Dados abertos - Sucupira - Teses e dissertações (2013 a 2016)Universidade Federal de São Paulo (UNIFESP)Gebrim, Luiz Henrique [UNIFESP]Universidade Federal de São Paulo (UNIFESP)Madeira, Marcelo [UNIFESP]2018-07-27T15:50:09Z2018-07-27T15:50:09Z2014-09-30info:eu-repo/semantics/doctoralThesisinfo:eu-repo/semantics/publishedVersion92 p.application/pdfhttps://sucupira.capes.gov.br/sucupira/public/consultas/coleta/trabalhoConclusao/viewTrabalhoConclusao.jsf?popup=true&id_trabalho=1775900MADEIRA, Marcelo. Receptor de estrogênio beta como marcador preditivo de resposta no tratamento neoadjuvante do carcinoma de mama com anastrozol e tamoxifeno. 2014. 92 f. Tese (Doutorado) - Escola Paulista de Medicina, Universidade Federal de São Paulo (UNIFESP), São Paulo, 2014.MARCELO MADEIRA.pdfhttps://repositorio.unifesp.br/handle/11600/46388porinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-08-06T13:59:36Zoai:repositorio.unifesp.br/:11600/46388Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-08-06T13:59:36Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.none.fl_str_mv Receptor de estrogênio beta como marcador preditivo de resposta no tratamento neoadjuvante do carcinoma de mama com anastrozol e tamoxifeno
Estrogen receptor alpha/beta ratio and estrogen receptor beta as predictors of endocrine therapy responsiveness–a randomized neoadjuvant trial comparison between anastrozole and tamoxifen for the treatment of postmenopausal breast cancer
title Receptor de estrogênio beta como marcador preditivo de resposta no tratamento neoadjuvante do carcinoma de mama com anastrozol e tamoxifeno
spellingShingle Receptor de estrogênio beta como marcador preditivo de resposta no tratamento neoadjuvante do carcinoma de mama com anastrozol e tamoxifeno
Madeira, Marcelo [UNIFESP]
cancer
estrogen receptor beta
receptor de estrogênio beta
receptor de estrogênio alfa
câncer de mama
tamoxifeno
inibidores da aromatase
terapia neoadjuvante
title_short Receptor de estrogênio beta como marcador preditivo de resposta no tratamento neoadjuvante do carcinoma de mama com anastrozol e tamoxifeno
title_full Receptor de estrogênio beta como marcador preditivo de resposta no tratamento neoadjuvante do carcinoma de mama com anastrozol e tamoxifeno
title_fullStr Receptor de estrogênio beta como marcador preditivo de resposta no tratamento neoadjuvante do carcinoma de mama com anastrozol e tamoxifeno
title_full_unstemmed Receptor de estrogênio beta como marcador preditivo de resposta no tratamento neoadjuvante do carcinoma de mama com anastrozol e tamoxifeno
title_sort Receptor de estrogênio beta como marcador preditivo de resposta no tratamento neoadjuvante do carcinoma de mama com anastrozol e tamoxifeno
author Madeira, Marcelo [UNIFESP]
author_facet Madeira, Marcelo [UNIFESP]
author_role author
dc.contributor.none.fl_str_mv Gebrim, Luiz Henrique [UNIFESP]
Universidade Federal de São Paulo (UNIFESP)
dc.contributor.author.fl_str_mv Madeira, Marcelo [UNIFESP]
dc.subject.por.fl_str_mv cancer
estrogen receptor beta
receptor de estrogênio beta
receptor de estrogênio alfa
câncer de mama
tamoxifeno
inibidores da aromatase
terapia neoadjuvante
topic cancer
estrogen receptor beta
receptor de estrogênio beta
receptor de estrogênio alfa
câncer de mama
tamoxifeno
inibidores da aromatase
terapia neoadjuvante
description Background: The role of estrogen receptor beta (ER-β) in breast cancer (BC) remains unclear. Some studies have suggested that ER-β may oppose the actions of estrogen receptor alpha (ER-α), and clinical evidence has indicated that the loss of ER-β expression is associated with a poor prognosis and resistance to endocrine therapy. The objective of the present study is to determine the role of ER-β and the ER-α/ER-β ratio in predicting the response to endocrine therapy and whether different regimens have any effect on ER-β expression levels. Methods: Ninety postmenopausal patients with primary BC were recruited for a short-term double-blinded randomized prospective controlled study. To determine tumor cell proliferation, the expression of Ki67 was measured in tumor biopsy samples taken before and after 26 days of treatment with anastrozole 1 mg/day (N = 25), tamoxifen 20 mg/day (N = 24) or placebo (N = 29) of 78 participants. The pre- and post-samples were placed in tissue microarray blocks and submitted immunohistochemical assay. Biomarker statuses (ER-β, ER-α and Ki67) were obtained by comparing each immunohistochemical evaluation of the pre- and post-surgery samples using the semi-quantitative Allred´s method. Statistical analyses were performed using an ANOVA and Spearman´s correlation coefficient tests, with significance at p ≤ 0.05. Results: The frequency of ER-β expression did not change after treatment (p = 0.33). There were no significant changes in Ki67 levels in ER-β-negative cases (p = 0.45), but in the ER-β-positive cases, the anastrozole (p = 0.01) and tamoxifen groups (p = 0.04) presented a significant reduction in post-treatment Ki67 scores. There was a weak but positive correlation between the ER-α and ER-β expression levels. Only patients with an ER-α/ER-β expression ratio between 1 and 1.5 demonstrated significant differences in Ki67 levels after treatment with anastrozole (p = 0.005) and tamoxifen (p = 0.026). Conclusions: These results provide additional data that indicate that the measurement of ER-β in BC patients may help predict tamoxifen and anastrozole responsiveness in the neoadjuvant setting. These effects of hormonal treatment appear to be dependent on the ratio of ER-α/ER-β expression.
publishDate 2014
dc.date.none.fl_str_mv 2014-09-30
2018-07-27T15:50:09Z
2018-07-27T15:50:09Z
dc.type.driver.fl_str_mv info:eu-repo/semantics/doctoralThesis
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format doctoralThesis
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://sucupira.capes.gov.br/sucupira/public/consultas/coleta/trabalhoConclusao/viewTrabalhoConclusao.jsf?popup=true&id_trabalho=1775900
MADEIRA, Marcelo. Receptor de estrogênio beta como marcador preditivo de resposta no tratamento neoadjuvante do carcinoma de mama com anastrozol e tamoxifeno. 2014. 92 f. Tese (Doutorado) - Escola Paulista de Medicina, Universidade Federal de São Paulo (UNIFESP), São Paulo, 2014.
MARCELO MADEIRA.pdf
https://repositorio.unifesp.br/handle/11600/46388
url https://sucupira.capes.gov.br/sucupira/public/consultas/coleta/trabalhoConclusao/viewTrabalhoConclusao.jsf?popup=true&id_trabalho=1775900
https://repositorio.unifesp.br/handle/11600/46388
identifier_str_mv MADEIRA, Marcelo. Receptor de estrogênio beta como marcador preditivo de resposta no tratamento neoadjuvante do carcinoma de mama com anastrozol e tamoxifeno. 2014. 92 f. Tese (Doutorado) - Escola Paulista de Medicina, Universidade Federal de São Paulo (UNIFESP), São Paulo, 2014.
MARCELO MADEIRA.pdf
dc.language.iso.fl_str_mv por
language por
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 92 p.
application/pdf
dc.publisher.none.fl_str_mv Universidade Federal de São Paulo (UNIFESP)
publisher.none.fl_str_mv Universidade Federal de São Paulo (UNIFESP)
dc.source.none.fl_str_mv reponame:Repositório Institucional da UNIFESP
instname:Universidade Federal de São Paulo (UNIFESP)
instacron:UNIFESP
instname_str Universidade Federal de São Paulo (UNIFESP)
instacron_str UNIFESP
institution UNIFESP
reponame_str Repositório Institucional da UNIFESP
collection Repositório Institucional da UNIFESP
repository.name.fl_str_mv Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)
repository.mail.fl_str_mv biblioteca.csp@unifesp.br
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