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Table 1 Frequency of genetic abnormalities by tumour type

From: Prognostic and predictive markers in recurrent high grade glioma; results from the BR12 randomised trial

 

Tumour grade

AOA

AA

GB

Total

N

%

N

%

N

%

N

%

Chromosome 1 status

 Normal copy number

3

50%

26

72%

127

56%

156

58%

 Trisomy

0

0%

0

0%

4

2%

4

1%

 Monosomy

0

0%

0

0%

0

0%

0

0%

 Any other abnormality

3

50%

10

28%

94

42%

107

40%

1p status

 Normal copy number

4

67%

28

78%

150

67%

182

68%

 Loss of 1 copy

1

17%

1

3%

2

1%

4

1%

 Any other abnormality

1

17%

7

19%

73

32%

81

30%

1p36 status

 Normal copy number

4

67%

31

86%

161

72%

196

73%

 Loss of 1 copy

1

17%

4

11%

49

22%

54

20%

 Loss of both regions

0

0%

0

0%

6

3%

6

2%

 Any other abnormality

1

17%

1

3%

9

4%

11

4%

Other abnormality

 No

4

67%

28

78%

160

71%

192

72%

 Yes

2

33%

8

22%

65

29%

75

28%

Chromosome 10 status

 Normal copy number

4

67%

14

39%

24

11%

42

16%

 Monosomy

0

0%

4

11%

146

65%

150

56%

 10q partial deletion

2

33%

14

39%

45

20%

61

23%

 Any other abnormality

0

0%

4

11%

10

4%

14

5%

PTEN

 Normal copy number

6

100%

26

72%

54

24%

86

32%

 Hemizygous deletion

0

0%

10

28%

162

72%

172

64%

 Homozygous deletion

0

0%

0

0%

9

4%

9

3%

MGMT

 Normal copy number

4

67%

15

42%

28

12%

47

18%

 Hemizygous deletion

2

33%

21

58%

196

87%

219

82%

 Homozygous deletion

0

0%

0

0%

1

0%

1

0%

 

6

100%

36

100%

225

100%

267

100%

Chromosome 7 status

 Normal copy number

3

50%

22

61%

36

16%

61

23%

 Trisomy/polysomy

0

0%

2

6%

143

64%

145

54%

 Monosomy

0

0%

0

0%

1

0%

1

0%

 Any other abnormality

3

50%

12

33%

45

20%

60

22%

Chromosome 19 status

 Normal copy number

4

67%

26

72%

135

60%

165

62%

 Trisomy

0

0%

4

11%

48

21%

52

19%

 Monosomy

0

0%

0

0%

4

2%

4

1%

 Any other abnormality

2

33%

6

17%

38

17%

46

17%

19q status

 Normal copy number

4

67%

27

75%

139

62%

170

64%

 Loss of 1 copy

1

17%

1

3%

2

1%

4

1%

 Any other abnormality

1

17%

8

22%

84

37%

93

35%

19q13 status

 Normal copy number

4

67%

27

75%

139

62%

170

64%

 Loss of 1 copy

0

0%

3

8%

20

9%

23

9%

 Any other abnormality

2

33%

6

17%

66

29%

74

28%

EGFR Amplification

 No

6

100%

32

89%

125

56%

163

61%

 Yes (>4 copies)

0

0%

4

11%

100

44%

104

39%

CDKN2A/p14 ARF

 Normal copy number

4

67%

24

67%

87

39%

115

43%

 Hemizygous deletion

2

33%

11

31%

67

30%

80

30%

 Homozygous deletion

0

0%

1

3%

71

32%

72

27%

MDM2 Amplification

 No

6

100%

34

94%

205

91%

245

92%

 Yes (>4 copies)

0

0%

2

6%

20

9%

22

8%

CDK4 amplification

 No

6

100%

33

92%

200

89%

239

90%

 Yes (>4 copies)

0

0%

3

8%

25

11%

28

10%

PDGFRA amplification

 No

6

100%

33

92%

211

94%

250

94%

 Yes (>4 copies)

0

0%

3

8%

14

6%

17

6%

RB1 copy number

 Normal

5

100%

31

86%

164

73%

200

75%

 Hemizygous deletion

0

0%

5

14%

60

27%

65

24%

 3 copies

0

0%

0

0%

1

0%

1

0%

TP53 mutation cases with complete dataset only

 No

2

40%

4

40%

43

64%

49

60%

 Yes

3

60%

6

60%

24

36%

33

40%

IDH1/IDH2 mutation

 No

1

17%

7

16%

191

82%

199

71%

 Yes

5

83%

36

84%

41

18%

82

29%

RB1 pathway

 Normal

3

60%

19

53%

52

23%

74

28%

 Abnormal

2

40%

17

47%

173

77%

192

72%

p53 pathway

 Normal

2

33%

2

7%

10

5%

14

6%

 Abnormal

4

67%

26

93%

181

95%

211

94%

MGMT Methylation

 <10%

0

0%

5

12%

66

28%

71

25%

 ≥10%

6

100%

36

88%

168

72%

210

75%

  1. AOA, Anaplastic oligoastrocytoma; AA, Anaplastic Astrocytoma; GB, Glioblastoma.