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Table 3 Anti-trastuzumab Ab levels developed in 32 patien’s serum samples and determined at two different points during trastuzumab treatment course

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

Sample code

No. of administered doses before 1st assay point

1st assay point titer

No. of administered doses before 2nd assay point

2nd assay point titer

  

Value

±SD

*Percentage of positive samples

 

Value

±SD

**Percentage of positive samples

T2–65

1

1.36

0.01

71.43%

12

ND

 

28.13%

T2–66

1.94

0.02

10

1.65

0.04

12

ND

 

T2–67

ND

 

10

ND

 

T2–68

1.61

0.02

16

ND

 

T2–69

ND

 

10

ND

 

T2–70

3.1

0.01

7

ND

 

T2–71

2.77

0.05

10

1.37

0.07

T2–72

2

ND

 

80%

12

ND

 

T2–73

1.78

0.06

14

2.25

0.01

T2–74

1.56

0.09

12

1.02

0.03

T2–75

3.07

0.05

14

2.4

0.04

T2–76

2.93

0.1

10

1.01

0.04

T2–77

3

ND

 

0%

8

ND

 

15

ND

 

T2–78

ND

 

17

ND

 

T2–79

ND

 

15

ND

 

T2–80

4

ND

 

33.33%

6

ND

 

T2–81

2.24

0.02

14

ND

 

T2–82

0.85

0.1

12

ND

 

T2–83

ND

 

16

ND

 

T2–84

ND

 

14

ND

 

T2–85

1.13

0.01

14

1.33

0.001

T2–86

6

ND

 

25%

13

ND

 

T2–87

ND

 

15

ND

 

T2–88

2.43

0.01

13

ND

 

T2–89

ND

 

14

ND

 

T2–90

7

2.63

0.16

67%

13

1.18

0.03

T2–91

ND

 

16

ND

 

T2–92

4.64

0.03

17

1.67

0.05

T2–93

8

ND

 

50%

17

ND

 

T2–94

0.85

0.01

15

ND

 

T2–95

1.29

0.08

16

ND

 

T2–96

1.95

0.06

16

ND

 
  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. **Percentage of positive samples was calculated from samples that gave titers ≥1 relative to the total number of samples in 2nd assay point