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Table 4 Correlation of basal cytotoxicity and ADCC with response to trastuzumab of neoadjuvant breast cancer patients

From: Analysis of in vitro ADCC and clinical response to trastuzumab: possible relevance of FcγRIIIA/FcγRIIA gene polymorphisms and HER-2 expression levels on breast cancer cell lines

NEO patients

pPR (n = 3)

P

pCR (n = 12)

P

P c

Cytotoxicity

Cytotoxicity

BASAL

ADCC

BASAL

ADCC

SKBR3

n = 3

n = 3

 

n = 11

n = 11

  

Present

1 (33.3)

3 (100.0)

0.400

4 (36.4)

9 (81.8)

0.080

0.240

Absent

2 (66.7)

0 (–)

 

7 (63.6)

2 (18.2)

  

BT474

n = 2

n = 2

 

n = 9

n = 9

  

Present

0 (–)

1 (50.0)

0.400

1 (11.1)

6 (66.7)

0.050

0.147

Absent

2 (100.0)

1 (50.0)

 

8 (88.9)

3 (33.3)

  

MCF-7

n = 2

n = 2

 

n = 11

n = 11

  

Present

0 (–)

2 (100.0)

0.333

2 (18.2)

10 (90.9)

0.002

0.006

Absent

2 (100.0)

0 (–)

 

9 (81.8)

1 (9.1)

  
  1. PBMCs were analyzed for their cytolytic activity in an ADCC assay using trastuzumab (2 µg/ml) and SKBR3, BT474 and MCF-7 cell lines at 20:1 effector to target cell ratio. PBMCs were incubated with target cells in medium alone (BASAL) or in the presence of trastuzumab (ADCC). Results are expressed as number and percentages (in brackets) of patients showing basal or trastuzumab-mediated cytotoxicity (cut off: >5 %)
  2. Comparison of BASAL cytotoxicity and ADCC was estimated using the Fisher’s test (P value) (significance level <0.05) and further adjusted with Bonferroni correction for multiple comparisons (P c value) in the indicated patients
  3. NEO neoadjuvant, ADCC antibody-dependent cellular cytotoxicity, pPR pathological partial response, pCR pathological complete response