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Table 2 Anti-trastuzumab Ab levels developed in 46 patien’s serum samples and determined at a single point during trastuzumab treatment course

From: Trastuzumab immunogenicity development in patients’ sera and in laboratory animals

Administered doses before blood sample withdrawal

Sample Code

Titer

*Percentage of positive samples

Value

±SD

1

T1–19

ND

 

33.33%

T1–20

4.61

0.62

T1–21

0.49

0.04

T1–22

ND

 

T1–23

3.64

0.02

T1–24

ND

 

2

T1–25

0.73

0.04

66.67%

T1–26

2.86

0.04

T1–27

6.65

1.78

3

T1–28

ND

 

75%

T1–29

1.27

0.02

T1–30

2.52

0.05

T1–31

5.31

0.07

4

T1–32

0.89

0.04

50%

T1–33

ND

 

T1–34

7.78

0.24

T1–35

8.18

0.60

5

T1–36

0.56

0.03

NVC

6

T1–37

ND

 

7

T1–38

ND

 

T1–39

1.07

0.07

8

T1–40

ND

 

33.33%

T1–41

ND

 

T1–42

ND

 

T1–43

2.03

0.1

T1–44

2.77

0.44

T1–45

ND

 

10

T1–46

ND

 

25%

T1–47

ND

 

T1–48

ND

 

T1–49

2.9

0.001

12

T1–50

ND

 

NVC

T1–51

ND

 

13

T1–52

ND

 

T1–53

ND

 

14

T1–54

3.36

0.06

16.67%

T1–55

ND

 

T1–56

ND

 

T1–57

0.98

0.08

T1–58

ND

 

T1–59

ND

 

15

T1–60

2.14

0.07

NVC

T1–61

0.99

0.03

16

T1–62

ND

 

T1–63

ND

 

17

T1–64

5.77

0.27

  1. *Percentage of positive samples was calculated from samples that gave titers ≥1 relative to the number of tested samples of patients administered the same number of doses
  2. ND no detected antibodies, NVC not valid for calculations