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Quantitative immunocytochemical profile to predict early outcome of disease in triple-negative breast carcinomas.

Abstract
We aimed in this study at identifying prognostic immunohistochemical molecular signatures indicative of disease outcome, also relevant for development of new specific therapies, in triple-negative (ER, PR, c-erbB2- negative) breast carcinoma subtypes. We evaluated 42 markers in tissue micro-arrays from a series of 924 breast carcinomas including 184 triple-negative tumors using standardized quantitative immunocytochemical assays and correlated the data with patients' outcome (mean follow-up of 79 months). When 27/42 markers including basal-like markers first found to be individually significant for prognosis in a univariate analysis (log-rank test) in 924 tumors, were secondly evaluated in the triple-negative tumor subtype (184/924), eleven including maspin, P21, P27, PTEN, caveolin, EGFR, FAK, P38, pMAPK, STAT1 and CD10 were 89.2% predictive of disease outcome in logistic regression. When markers reported in the literature as expressed in basal-like subtype were evaluated in the 924 series, only eight (EGFR, CK14, moesin, caveolin, cMet, ckit, CD44v6, C10) were prognosis predictive in univariate analysis (log-rank test) and in logistic regression were predictive of disease outcome in 66.3% independently of ER, PR and c-erbB2 expression and in 72% in triple-negative tumor subset. The results suggest that the category of 'triple-negative' breast carcinomas does not exactly overlap the basal-like subtype, and that immunoprofiling of triple-negative tumors (not similar to that of basal-like tumors) may be helpful to select patients for more aggressive treatment and provides a basis for development of tailored therapy.
AuthorsColette Charpin, Sophie Giusiano, Véronique Secq, Séverine Carpentier, Lucile Andrac, Marie-Noëlle Lavaut, Claude Allasia, Pascal Bonnier, Stéphane Garcia
JournalInternational journal of oncology (Int J Oncol) Vol. 34 Issue 4 Pg. 983-93 (Apr 2009) ISSN: 1019-6439 [Print] Greece
PMID19287955 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Topics
  • Area Under Curve
  • Breast Neoplasms (metabolism, mortality, therapy)
  • Carcinoma (metabolism, mortality, therapy)
  • Gene Expression Regulation, Neoplastic
  • Humans
  • Immunohistochemistry (methods)
  • Neoplasm Metastasis
  • Phenotype
  • Prognosis
  • ROC Curve
  • Recurrence
  • Regression Analysis
  • Sensitivity and Specificity
  • Treatment Outcome

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