clinicopathological analysis of patients with breast cancer and their families
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abstract
background: breast cancer is one of the most common malignancies among iranian women; however, its clinicopathological feature is uncertain. we pioneered a genetic counseling program among patients with breast cancer and their families in isfahan. this is the first report of this program. methods: this was a descriptive cross-sectional study on women with breast cancer registered in ala cancer control and prevention center (accpc)during 2014. the women and/or their first/second relatives were enrolled for genetic counseling, then their demographic and clinicopathological data were analyzed using spsssoftware. results: the records of 258 patients with breast cancer and their families were studied. the mean age of the patients at diagnosis was 44.2 years (range: 25-71 years). of these, 88 (34.1%) patients had ≤40 years at diagnosis. only 2 (0.8%) patients were men. also, 21 (8.1%) out of the 258 patients had died at the time of genetic counseling. distant metastasis was found in 40 (15.5%) patients at diagnosis. the most common pathological feature of breast tumor was invasive ductal carcinoma (68.2%) and the rarest were sarcoma (0.4%) and papillary carcinoma (0.4%). triple-negative molecular phenotype breast cancer was reported in 25 (9.7%) patients. estrogen receptor (er), progesterone receptor (pr) and human epidermal growth factor receptor 2 (her2) were negative in 32.2%, 27.1%, and 44.2% of the patients' tumors, respectively. p53 had been checked in 41.5% of the patients of which about 70.1% were mutant. overall, 895 cases of cancer were reported among the patients and their families (3.5 patients per family: range=1-9) of which breast, gastric, and colorectal cancers with an incidence of 43.9%, 8.3% and 5.5%, were the most common malignancies, respectively. conclusion: early-onset breast cancer and positive family history for cancer were seen in a significant proportion of the patients in our center, indicating the importance of genetic counseling among the patients and their families.
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Journal title:
iranian journal of blood and cancerجلد ۸، شماره ۱، صفحات ۱۷-۲۲
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