Teste de receptores de estrógeno e progesterona em carcinoma de mama

concordância dos resultados entre laboratórios locais e de referência no Brasil

Autores

  • Sheila Cristina Lordelo Wludarski Pathology Consultancy
  • Lisandro Ferreira Lopes Pathology Consultancy
  • Ívison Xavier Duarte Pathology Consultancy
  • Filomena Marino Carvalho Pathology Consultancy
  • Lawrence Weiss Pathology Consultancy
  • Carlos Eduardo Bacchi Pathology Consultancy

Palavras-chave:

Neoplasias da mama, Receptores estrogênicos, Receptores de progesterona, Imunoistoquímica, Brasil

Resumo

CONTEXTO E OBJETIVO: O carcinoma de mama é responsável por cerca de um quarto de todos os cânceres em mulheres. O teste de receptores de estrógeno e progesterona se tornou parte essencial da avaliação clínica de pacientes com carcinoma de mama; assim, resultados precisos são fundamentais para identificação de pacientes que podem se beneficiar da terapia hormonal. O presente estudo tem por objetivo investigar a concordância nos resultados do teste de receptores hormonais entre um laboratório referência e laboratórios locais (ou comunitários) do Brasil. TIPO DE ESTUDO E LOCAL: Estudo retrospectivo em laboratório referência em patologia no Brasil. MÉTODOS: A concordância nos resultados dos testes de receptores hormonais entre um laboratório referência e 146 diferentes laboratórios locais brasileiros foi comparada em 500 casos de carcinoma invasivo de mama através da imunoistoquímica. RESULTADOS: Houve concordância de 89,4% (447/500 casos) e 85,0% (425/500 casos) nos resultados dos testes de receptores de estrógeno (k = 0,744, P < 0,001) e progesterona (k = 0,688, P < 0,001), respectivamente, entre laboratórios locais e referência, similar à descrita em outros países. A taxa de resultados falso-negativos nos testes de receptores de estrógeno e progesterona em laboratórios locais foi de 8,7% e 14,4%, respectivamente. A taxa de resultados falso-positivos nos testes de receptores de estrógeno e progesterona em laboratórios locais foi de 15,5% e 16,0%, respectivamente. CONCLUSÃO: Questões técnicas e de interpretação dos resultados podem explicar a maior parte das discordâncias nos testes de receptores hormonais em laboratórios locais. A validação dos testes de receptores de estrógeno e progesterona pelos laboratórios locais com medidas de controle de qualidade rigorosas é fortemente recomendada de modo a evitar o tratamento errôneo de pacientes com carcinoma de mama.

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Biografia do Autor

Sheila Cristina Lordelo Wludarski, Pathology Consultancy

MD. Associate Pathologist, Pathology Consultancy, Botucatu, São Paulo, Brazil.

Lisandro Ferreira Lopes, Pathology Consultancy

MD. Associate Pathologist, Pathology Consultancy, Botucatu, São Paulo, Brazil.

Ívison Xavier Duarte, Pathology Consultancy

MD. Associate Pathologist, Pathology Consultancy, Botucatu, São Paulo, Brazil.

Filomena Marino Carvalho, Pathology Consultancy

MD, PhD. Associate Professor, Department of Pathology, Faculdade de Medicina da Universidade de São Paulo (FMUSP), São Paulo, Brazil.

Lawrence Weiss, Pathology Consultancy

MD, PhD. Chair, Division of Pathology, City of Hope National Medical Center, Duarte, California, United States.

Carlos Eduardo Bacchi, Pathology Consultancy

MD, PhD. Director and Chief Pathologist, Pathology Consultancy, Botucatu, São Paulo, Brazil.

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Publicado

2011-07-07

Como Citar

1.
Wludarski SCL, Lopes LF, Duarte Ívison X, Carvalho FM, Weiss L, Bacchi CE. Teste de receptores de estrógeno e progesterona em carcinoma de mama: concordância dos resultados entre laboratórios locais e de referência no Brasil. Sao Paulo Med J [Internet]. 7º de julho de 2011 [citado 10º de março de 2025];129(4):236-42. Disponível em: https://periodicosapm.emnuvens.com.br/spmj/article/view/1606

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