Skip to main content
. 2018 Nov 7;13(6):757–767. doi: 10.1007/s11523-018-0602-1

Table 1.

Correlations between stromal tumor-infiltrating lymphocytes and clinicopathologic characteristics in HER2-positive breast cancers

Variables No. of patients (%) p value of sTILs
Total number of patients 143 (100)
Age (years)
 < 50 64 (44.8) 0.574
 ≥ 50 79 (55.2)
Tumor size (cm)
 ≤ 2 16 (11.2) 0.824
 2–5 96 (67.1)
 > 5 31 (21.7)
Histological gradea
 2 65 (45.5) 0.402
 3 78 (54.5)
Ki-67 index (%)b
 ≤ 10 9 (6.3) 0.166
 10–30 47 (32.9)
 > 30 87 (60.8)
Nodal status
 Negative 57 (39.9) <0.001
 Positive 86 (60.1)
Lympho-vascular invasion
 Negative 109 (76.2) 0.009
 Positive 34 (23.8)
MP gradingc
 1 7 (4.9) 0.002
 2 16 (11.2)
 3 10 (7.0)
 4 18 (12.6)
 5 92 (64.3)
Pathological response
 pCR 86 (60.1) < 0.001
 Non-pCR 57 (39.9)

HER2 Human epidermal growth factor receptor 2, sTILs tumor-Infiltrating lymphocytes, pCR pathological complete response

aThe histological grade of tumor was evaluated in pre-neoadjuvant chemotherapy (NAC) core needle biopsy specimens using the Nottingham grading system, with 3 being the worst score

bFraction of Ki-67-positive tumor cells

cMiller–Payne grading system; a histopathological classification system used to categorize tumor response to treatment relative to tumor cellularity in the pre-treatment section, with grade 1 indicating no reduction in overall cellularity and grade 5 indicating no invasive carcinoma