331 (7.9%) |
VM group tended to have a lower 60-month survival rate than the non-VM group |
p = 0.071 |
(18) |
|
VM group tended to have a higher hematogenous metastases than the non-VM group |
p = 0.059 |
|
90 (28.6%) |
VM correlated with lymph node metastases |
p = 0.004 |
(26) |
|
Histological grade |
p < 0.001 |
|
|
Nottingham prognostic index (NPI) (worse prognosis) |
p < 0.001 |
|
|
No correlated with the presence of: |
|
|
|
ER |
p = 0.391 |
|
|
PR |
p = 0.321 |
|
|
Her2 |
p = 0.114 |
|
|
VM correlated with overall survival |
p < 0.001 |
|
|
And disease-free survival |
p < 0.001 |
|
200 (30%) |
VM and Osteopontin co-expression correlated with pathological complete response |
p = 0.006 |
(27) |
202 (16.8%) |
VM presence was higher in TNBC vs. non TNBC |
p = 0.003 |
(28) |
|
VM correlated with worst |
p < 0.001 |
|
|
Disease free survival and overall survival |
p = 0.015 |
|
134 (30.6%) |
VM presence was higher in TNBC vs. non TNBC |
p = 0.004 |
(29) |
100 (29%) |
VM presence was higher in TNBC vs. non TNBC |
p = 0.020 |
(30) |
|
VM correlated with poorer overall survival |
p = 0.015 |
|
174 (24.7%) |
VM presence was higher in TNBC vs. non TNBC |
p = 0.044 |
(31) |
120 (22.5%) |
VM correlated with positive node status; |
p = 0.027 |
(32) |
|
a higher tumor stage |
p = 0.022 |
|
|
and higher levels of HER2 |
p = 0.018 |
|
|
VM did not correlate with ERalpha or PR status |
p = 0.143 |
|