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D2-40 in breast cancer: should we detect more vascular emboli?

Abstract
Peritumoral emboli assessed on hematoxylin-eosin-stained slides are taken into account for treatment of patients with operable breast cancer. We assessed whether immunostaining with D2-40 improves the prognostic significance of emboli in a group of tumors with a large immunohistochemical sampling and a long-term follow-up. Topography, number, and extension of hematoxylin-eosin and D2-40 emboli were compared in 94 node-negative breast cancers (median number of immunostained slides per tumor: 3). Metastasis-free survival of patients with or without hematoxylin-eosin and/or D2-40 emboli were evaluated (median follow-up of 178 months). Hematoxylin-eosin emboli were detected in 14 (15%) tumors and were located at distance from the tumor. D2-40 emboli were detected in 39 (41%) tumors and was often multiple (n=30), extensive (n=23), located within (n=13), close to (n=10) or at distance from the tumor (n=16). The 12 distant hematoxylin-eosin and D2-40 emboli were located in the same vessels (seven missed at the first hematoxylin-eosin examination and secondarily diagnosed by D2-40 staining). A difference in metastasis-free survival was found only between patients with no D2-40 emboli and those with distant D2-40 emboli (P=0.02). D2-40 emboli located within or close to the tumor had no prognostic value. Comparing the metastasis-free survival of patients with or without hematoxylin-eosin emboli, the prognostically unfavorable significance of hematoxylin-eosin emboli was improved when taking into account the seven patients with missed emboli at the first examination and secondarily diagnosed by D2-40 staining (P=0.006 vs 0.003). To conclude, D2-40 increases the diagnostic sensitivity of emboli in breast carcinoma and the high incidence of D2-40 emboli might be related to the number of immunostained slides per case. Nevertheless, only distant D2-40+ emboli had a prognostic impact. In practice, D2-40 might be useful to detect missed hematoxylin-eosin emboli especially in cases without any other prognostically unfavorable criterion.
AuthorsIsabelle de Mascarel, Gaëtan MacGrogan, Marc Debled, Ghislaine Sierankowski, Véronique Brouste, Simone Mathoulin-Pélissier, Louis Mauriac
JournalModern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc (Mod Pathol) Vol. 22 Issue 2 Pg. 216-22 (Feb 2009) ISSN: 1530-0285 [Electronic] United States
PMID18820667 (Publication Type: Comparative Study, Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Antibodies, Monoclonal
  • Antibodies, Monoclonal, Murine-Derived
  • Antigens, Tumor-Associated, Carbohydrate
  • Coloring Agents
  • monoclonal antibody D2-40
  • Eosine Yellowish-(YS)
  • Hematoxylin
Topics
  • Antibodies, Monoclonal
  • Antibodies, Monoclonal, Murine-Derived
  • Antigens, Tumor-Associated, Carbohydrate (analysis)
  • Blood Vessels (immunology, pathology)
  • Breast Neoplasms (diagnosis, immunology, pathology, therapy)
  • Carcinoma (diagnosis, immunology, pathology, therapy)
  • Coloring Agents
  • Embolism (diagnosis, immunology, pathology)
  • Eosine Yellowish-(YS)
  • False Negative Reactions
  • Female
  • Hematoxylin
  • Humans
  • Immunohistochemistry (methods)
  • Kaplan-Meier Estimate
  • Lymphatic Metastasis
  • Lymphatic Vessels (immunology, pathology)
  • Middle Aged
  • Neoplasm Invasiveness
  • Neoplasm Metastasis
  • Neoplastic Cells, Circulating (immunology, pathology)
  • Predictive Value of Tests
  • Reproducibility of Results
  • Staining and Labeling (methods)
  • Time Factors
  • Treatment Outcome

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