Table 1 Characteristics of patients with CML-BC.

From: Clonal evolution and clinical implications of genetic abnormalities in blastic transformation of chronic myeloid leukaemia

Number of cases

136

Age at BC diagnosis (y), median (range) (n = 126)

50 (16–86)

Sex, n (%) (n = 132)

 

  Male

79 (59.8)

  Female

53 (40.2)

Lineage of blasts, n (%) (n = 129)

 

  Myeloid

81 (62.8)

  Lymphoid

48 (37.2)

WBC (×103/uL), median (range) (n = 123)

40,600 (1700–580,000)

Hb (g/dL), median (range) (n = 123)

9.6 (5.0–15.8)

PLT (×103/uL), median (range) (n = 123)

105,000 (3000–2,740,000)

LDH (U/L), median (range) (n = 79)

696 (75–6332)

Blasts in BM (%), median (range) (n = 126)

59.5 (1.0–98.4)

Prior history of CP diagnosis, n (%) (n = 135)

 

  Yes

103 (76.3)

  No

32 (23.7)

Time from CP diagnosis (m), median (range) (n = 93)

34.3 (0.27–363)

Age at CP diagnosis (y), median (range) (n = 92)

45 (14–85)

Prior TKI before BC, n (%) (n = 134)

 

  Yes

57 (42.5)

  No

77 (57.5)

TKIs used for CP, n (%) (n = 53)

 

  Imatinib

50 (94.3)

  Dasatinib

2 (3.8)

  Nilotinib

1 (1.9)

TKI-based therapy for BC, n (%) (n = 119)

 

  Yes

72 (60.5)

  No

47 (39.5)

TKIs used for BC, n (%) (n = 72)

 

  Imatinib

36 (50.0)

  Dasatinib

32 (44.4)

  Nilotinib

2 (2.8)

  Ponatinib

2 (2.8)

Final status, n (%) (n = 123)

 

  Alive

26 (21.1)

  Dead

97 (78.9)

Method, n (%) (n = 136)

 

  Whole-exome sequencing

76 (55.9)

  Targeted capture sequencing

60 (44.1)

Median follow-up time (m), median (range) (n = 123)

38.2 (0.13–365)