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Table 1 Baseline patient characteristics (ITT population)

From: A multicenter real-world evidence study in the Swiss treatment landscape of chronic myeloid leukemia

1 L treatmenta

ITT

Imatinib

N = 26

Nilotinib

N = 27

Dasatinib

N = 8

Ponatinib

N = 1

Imatinib (gen)

N = 1

Total

N = 63

Men, n (%)

13 (50)

15 (56)

6 (75)

1 (100)

0 (0)

35 (56)

Median age at diagnosis, years (IQR)

60 (40–75)

45 (38–65)

56 (50–61)

74

24

55 (40–68)

Sokal risk group at diagnosis, %

 Low

15

26

0

0

0

N.A.

 Intermediate

42

26

63

100

0

 High

27

37

38

0

0

 Unknown

15

11

0

0

100

Median Sokal score at diagnosis, score (IQR), n

1.04 (0.92–1.43), n = 19

1.16 (0.83–1.46), n = 16

1.14 (0.86–1.83), n = 6

– , n = 0

– , n = 0

1.10 (0.88–1.46), n = 41

Transcript type, n (%)

 e13a2 (b2a2)

10 (38)

9 (33)

2 (25)

0 (0)

0 (0)

21 (33)

 e14a2 (b3a2)

12 (46)

9 (33)

5 (63)

1 (100)

0 (0)

27 (43)

 both

3 (12)

1 (4)

1 (12)

0 (0)

0 (0)

5 (8)

 unknown

1 (4)

8 (30)

0 (0)

0 (0)

1 (100)

10 (16)

Inclusion in clinical trial, n (%)

1 (4)

7 (26)

0 (0)

1 (100)

0 (0)

9 (14)

Median daily dose, mg (IQR)

400 (400–400)

600 (600–600)

100 (100–100)

45

400

  1. There were no statistically significant differences between the groups for sex, age at diagnosis and median Sokal score (p > 0.05)
  2. IQR interquartile range, ITT intention to treat population, N.A. not available
  3. aNo patient had been treated with 1 L bosutinib. The transcript type was determined by qualitative PCR