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. 2011 May 15;11(10):853–865. doi: 10.4161/cbt.11.10.15177

Table 2.

Frequency distribution of clinical and tumor features for N = 99 cases

Breast diagnosis N (%) Percent × 100
CIS 11 11
DCIS-mINV 15 15
Invasive carcinoma 73 73
Tumor stage
TIS 11 11
T1 53 53
T2 30 30
T3 5 5
Tumor grade
I 10 10
II 71 70
III 15 15
LCIS 3 3
Bilateral breast Dx
Yes 19 19
No 80 80
Metastatic disease
Yes 17 17
No 82 82
Recurrence
Yes 24 24
No 75 75
Age of cancer onset
<30 4 4
30–39 19 19
40–49 43 43
50–59 28 28
60–69 4 4
70–79 1 1
Lymph node status
Positive 27 27
Negative 72 72
ER IHC status
Positive 60 60
Negative 28 28
ND 11 11
PR IHC status
Positive 63 63
Negative 24 24
ND 12 12
HER2 IHC status
Positive 21 21
Negative 36 36
ND 42 42
Deceased
Yes 13 13
No 86 86
BRCA mutation status
BRCA+ 11 11
UNK 7 7
VUS 6 6
NEG 26 26
NT 49 49

Breast diagnosis: CIS, carcinoma in situ; DCIS-mINV, case diagnosed with a <1.0 cm micro-invasive carcinoma, but for which only DCIS remained on the tissue block; IC, invasive carcinoma. Lymph node status: indicates if lymph nodes were positive or negative for tumor cells at initial diagnosis of breast cancer. ER, PR and HER2 status: IHC tumor staining with antibodies to the estrogen and progesterone receptors, and HER2 growth factor receptor, respectively. BRCA mutation status: genetic mutation testing of BRCA1 and BRCA2 genes; BRCA+, carrier of a known deleterious BRCA1 or BRCA2 mutation; UNK, test results unknown. By report, the individual underwent BRCA mutation testing, but the test result was not reported in any of the three Johns Hopkins clinical databases abstracted in the study. VUS, variant of unknown significance; e.g., a BRCA gene mutation was found, but no population data as yet exists to determine if the mutation is deleterious; NEG, negative, the patient did not carry a BRCA1 or BRCA2 gene mutation. NT, not tested.