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Piotr Potemski, Elżbieta Płuciennik, Andrzej K. Bednarek, Renata Kusińska, Grażyna Pasz-Walcza, Dorota Jesionek-Kupnicka, Cezary Watała, Radzisław Kordek
Med Sci Monit 2006; 12(12): MT57-61
Background: The most commonly used methods for detecting HER2 gene amplifi cation in breast cancer are immunohistochemistry and fl uorescence in-situ hybridization. The aim of this retrospective study was to assess HER2 expression by real-time RT-PCR.
Material/Methods: Expression of HER2 was analyzed by real-time RT-PCR and immunohistochemistry in specimens of invasive ductal breast cancer tissue obtained from 131 women during radical mastectomy.
Results: There was a highly signifi cant difference in mean relative gene expression between HER2-positive and HER2-negative patients as assessed by immunostaining (22.10±41.89 vs. 3.17±8.76; p<0.001). With a median follow-up of 56 months, the cancer-specific survival of HER2-positive patients assessed by RT-PCR was worse in all cases and in the node-positive group. In multivariate analysis, HER2 status was an independent prognostic factor in all patients.
Conclusions: Real-time RT-PCR is a valuable method for determining HER2 status, but the selection of the cut-off point of the relative gene expression differentiating between HER2-negative and -positive tumors is essential.