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Article Open Access

Outcome of Epstein-Barr virus-associated primary breast cancer

  • Authors:
    • Chafika Mazouni
    • Frédéric Fina
    • Sylvie Romain
    • L'Houcine Ouafik
    • Pascal Bonnier
    • Pierre‑Marie Martin
  • View Affiliations / Copyright

    Affiliations: Transfer Laboratory of Biological Oncology, Public Assistance Hospitals of Marseille, Northern Faculty of Medicine, Marseille, France, Institute of Surgery and Gynecological and Breast Oncology, Beauregard Hospital, Marseille, France
    Copyright: © Mazouni et al. This is an open access article distributed under the terms of Creative Commons Attribution License.
  • Pages: 295-298
    |
    Published online on: November 20, 2014
       https://doi.org/10.3892/mco.2014.459
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Abstract

The presence of the Epstein‑Barr‑virus (EBV) has been reported to be a pathogenic factor in breast cancer (BC). We previously demonstrated the aggressiveness of EBV‑positive BC. The purpose of the present study was to evaluate the effect of EBV on the prognosis of BC according to the BC phenotype. A total of 117 patients with primary BC previously tested for the presence of EBV were evaluated. The presence of the virus was evaluated in breast specimens using quantitative PCR (qPCR). Disease‑free survival (DFS) and overall survival (OS) were evaluated for 4 molecular subtypes, namely luminal A and B (lumA and lumB, respectively), human epidermal growth factor receptor 2 (HER2) and triple‑negative (TN) subtypes and according to the EBV status. EBV positivity was observed in 32.5% of the cases. TN, HER2 and lumB tumours were more frequent among EBV‑BC cases (P=0.02). The DFS rates were different between BC subtypes (P=0.002), but the differences were not statistically significant when the cases were stratified according to the EBV status (P=0.08 for EBV‑negative and 0.06 for EBV‑positive cases). The OS rates were similar for BC subtypes (P=0.50) and when the cases were stratified according to the EBV status (P=0.16 and P=0.67 for EBV-positive and -negative cases, respectively). EBV was not associated with DFS or OS, in contrast to BC phenotypes, tumour size or nodal status. Therefore, EBV positivity was found to exert no effect on survival, despite its association with aggressive BC phenotypes.
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Copy and paste a formatted citation
Spandidos Publications style
Mazouni C, Fina F, Romain S, Ouafik L, Bonnier P and Martin PM: Outcome of Epstein-Barr virus-associated primary breast cancer. Mol Clin Oncol 3: 295-298, 2015.
APA
Mazouni, C., Fina, F., Romain, S., Ouafik, L., Bonnier, P., & Martin, P. (2015). Outcome of Epstein-Barr virus-associated primary breast cancer. Molecular and Clinical Oncology, 3, 295-298. https://doi.org/10.3892/mco.2014.459
MLA
Mazouni, C., Fina, F., Romain, S., Ouafik, L., Bonnier, P., Martin, P."Outcome of Epstein-Barr virus-associated primary breast cancer". Molecular and Clinical Oncology 3.2 (2015): 295-298.
Chicago
Mazouni, C., Fina, F., Romain, S., Ouafik, L., Bonnier, P., Martin, P."Outcome of Epstein-Barr virus-associated primary breast cancer". Molecular and Clinical Oncology 3, no. 2 (2015): 295-298. https://doi.org/10.3892/mco.2014.459
Copy and paste a formatted citation
x
Spandidos Publications style
Mazouni C, Fina F, Romain S, Ouafik L, Bonnier P and Martin PM: Outcome of Epstein-Barr virus-associated primary breast cancer. Mol Clin Oncol 3: 295-298, 2015.
APA
Mazouni, C., Fina, F., Romain, S., Ouafik, L., Bonnier, P., & Martin, P. (2015). Outcome of Epstein-Barr virus-associated primary breast cancer. Molecular and Clinical Oncology, 3, 295-298. https://doi.org/10.3892/mco.2014.459
MLA
Mazouni, C., Fina, F., Romain, S., Ouafik, L., Bonnier, P., Martin, P."Outcome of Epstein-Barr virus-associated primary breast cancer". Molecular and Clinical Oncology 3.2 (2015): 295-298.
Chicago
Mazouni, C., Fina, F., Romain, S., Ouafik, L., Bonnier, P., Martin, P."Outcome of Epstein-Barr virus-associated primary breast cancer". Molecular and Clinical Oncology 3, no. 2 (2015): 295-298. https://doi.org/10.3892/mco.2014.459
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