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Breast Cancers With Brain Metastases are More Likely to be Estrogen Receptor Negative, Express the Basal Cytokeratin CK5/6, and Overexpress HER2 or EGFR
260
Citations
34
References
2006
Year
Breast OncologyOncologyCancer EpidemiologyBrain MetastasesBreast Cancer PatientsMedicineCancer GrowthPathologyGynecologyCancer PrognosisEstrogen Receptor NegativeBreast CancerTissue MicroarrayBreast CancersCancer BiologyRadiation OncologyTumor BiologyEndocrine-related Cancer
Brain metastases from breast cancer cause significant morbidity and mortality. The study aims to identify clinical‑pathologic markers that flag breast cancer patients at high risk for brain metastases at diagnosis. Primary tumors from 55 patients who developed brain metastases were assembled into a tissue microarray, immunostained for ER, HER2, CK5/6, and EGFR, and compared to tumors from 254 non‑metastatic patients and 40 patients with other metastatic sites. Patients who developed brain metastases were more likely to be under 50, have ER‑negative, high‑grade tumors, and express CK5/6, EGFR, and HER2.
Brain metastases (BM) from breast cancer are associated with significant morbidity and mortality. In the current study, we have examined a cohort of breast cancer patients who went on to develop BM for clinical-pathologic features and predictive markers that identify this high-risk subgroup of patients at the time of diagnosis. The primary tumors from 55 patients who developed BM were used to construct a tissue microarray. The clinical and pathologic features were recorded and the tissue microarray was stained for estrogen receptor, human epidermal growth factor receptor 2, cytokeratin 5/6, and epidermal growth factor receptor by immunohistochemistry. This cohort of patients was compared against a group of 254 patients who remain free of metastases (67 mo mean follow-up), and another cohort of 40 patients who developed mixed visceral and bone metastatic disease without brain recurrence over a similar period of time. Breast cancer patients who went on to develop BM were more likely to be <50 years old (P<0.001), and the primary tumors were more likely to be estrogen receptor negative (P<0.001) and high grade (P=0.002). The primary tumors were also more likely to express cytokeratin 5/6 (P<0.001) and epidermal growth factor receptor (P=0.001), and to overexpress human epidermal growth factor receptor 2 (P=0.001). The data presented above suggest a profile for breast cancer patients at increased risk for developing BM. Predictive factors to help identify patients with metastatic breast cancer who are at an increased risk for developing central nervous system recurrence might allow for screening of this population for early detection and treatment or for the development of targeted strategies for prevention.
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