Table 3 |
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|
Classification of ER+ intrinsic subtypes, medullary breast cancer, and BRCA1 tumors into ER- subclasses |
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|
ER+ |
MBC |
DBC |
BRCA1 |
|||||
|
|
||||||||
|
Luminal B |
Luminal A |
Normal |
Basal |
HER2 |
||||
|
|
||||||||
|
n |
97 |
337 |
32 |
19 |
42 |
22 |
44 |
18 |
|
n classifiable |
37 |
113 |
19 |
17 |
16 |
20 |
33 |
16 |
|
CC+/IR+ |
17 |
2 |
0 |
13 |
11 |
14 |
4 |
13 |
|
CC+ |
20 |
2 |
0 |
4 |
1 |
3 |
3 |
2 |
|
ECM+ |
0 |
71 |
16 |
0 |
0 |
1 |
3 |
1 |
|
SR+ |
0 |
9 |
0 |
0 |
0 |
0 |
20 |
0 |
|
IR+ |
0 |
29 |
3 |
0 |
4 |
2 |
3 |
0 |
|
|
||||||||
|
Classification of ER+ intrinsic subtypes (527 samples from the integrated cohort NKI2 + EMC + NCH), 22 medullary breast cancers (MBCs) and 44 ductal breast cancers (DBCs) from [38], and 18 BRCA1 mutants from [3] into ER- subclasses, using the nearest centroid criterion with Pearson correlation as distance metric. Only samples with Pearson correlation coefficients larger than 0.25 were deemed classifiable. ER, estrogen receptor. |
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|
Teschendorff et al. Genome Biology 2007 8:R157 doi:10.1186/gb-2007-8-8-r157 |
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