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Discordant Marker Expression Between Invasive Breast Carcinoma and Corresponding Synchronous and Preceding DCIS.
Visser, Lindy L; Elshof, Lotte E; Van de Vijver, Koen; Groen, Emma J; Almekinders, Mathilde M; Sanders, Joyce; Bierman, Carolien; Peters, Dennis; Hofland, Ingrid; Broeks, Annegien; van Leeuwen, Flora E; Rutgers, Emiel J Th; Schmidt, Marjanka K; Schaapveld, Michael; Lips, Esther H; Wesseling, Jelle.
Afiliação
  • Visser LL; Division of Molecular Pathology.
  • Elshof LE; Division of Molecular Pathology.
  • Van de Vijver K; Division of Psychosocial research and Epidemiology.
  • Groen EJ; Department of Surgery.
  • Almekinders MM; Department of Pathology, Division of Diagnostic Oncology.
  • Sanders J; Division of Molecular Pathology.
  • Bierman C; Department of Pathology, Division of Diagnostic Oncology.
  • Peters D; Division of Molecular Pathology.
  • Hofland I; Department of Pathology, Division of Diagnostic Oncology.
  • Broeks A; Department of Pathology, Division of Diagnostic Oncology.
  • van Leeuwen FE; Department of Pathology, Division of Diagnostic Oncology.
  • Rutgers EJT; Core Facility Molecular Pathology and Biobanking, Division of Molecular Pathology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.
  • Schmidt MK; Core Facility Molecular Pathology and Biobanking, Division of Molecular Pathology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.
  • Schaapveld M; Core Facility Molecular Pathology and Biobanking, Division of Molecular Pathology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.
  • Lips EH; Division of Psychosocial research and Epidemiology.
  • Wesseling J; Department of Surgery.
Am J Surg Pathol ; 43(11): 1574-1582, 2019 11.
Article em En | MEDLINE | ID: mdl-31206365
ABSTRACT
Ductal carcinoma in situ (DCIS) is considered a potential precursor of invasive breast carcinoma (IBC). Studies aiming to find markers involved in DCIS progression generally have compared characteristics of IBC lesions with those of adjacent synchronous DCIS lesions. The question remains whether synchronous DCIS and IBC comparisons are a good surrogate for primary DCIS and subsequent IBC. In this study, we compared both primary DCIS and synchronous DCIS with the associated IBC lesion, on the basis of immunohistochemical marker expression. Immunohistochemical analysis of ER, PR, HER2, p53, and cyclo-oxygenase 2 (COX-2) was performed for 143 primary DCIS and subsequent IBC lesions, including 81 IBC lesions with synchronous DCIS. Agreement between DCIS and IBC was assessed using kappa, and symmetry tests were performed to assess the pattern in marker conversion. The primary DCIS and subsequent IBC more often showed discordant marker expression than synchronous DCIS and IBC. Strikingly, 18 of 49 (36%) women with HER2-positive primary DCIS developed an HER2-negative IBC. Such a difference in HER2 expression was not observed when comparing synchronous DCIS and IBC. The frequency of discordant marker expression did not increase with longer time between primary DCIS and IBC. In conclusion, comparison of primary DCIS and subsequent IBC yields different results than a comparison of synchronous DCIS and IBC, in particular with regard to HER2 status. To gain more insight into the progression of DCIS to IBC, it is essential to focus on the relationship between primary DCIS and subsequent IBC, rather than comparing IBC with synchronous DCIS.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Biomarcadores Tumorais / Carcinoma Ductal de Mama / Carcinoma Intraductal não Infiltrante / Neoplasias Primárias Múltiplas Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans Idioma: En Revista: Am J Surg Pathol Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Biomarcadores Tumorais / Carcinoma Ductal de Mama / Carcinoma Intraductal não Infiltrante / Neoplasias Primárias Múltiplas Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans Idioma: En Revista: Am J Surg Pathol Ano de publicação: 2019 Tipo de documento: Article
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